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CURRICULUM VITAE
Part I
General Information
DATE PREPARED
09/23/11
Name:
Sabina Signoretti, M.D.
Office Address:
Department of Pathology,
Brigham and Women’s Hospital, Thorn 504A
75 Francis Street
Boston MA 02115
Ph : 617-525-7437
e-mail: [email protected]
Home Address:
77 Wenham Street Apt.2, Jamaica Plain, MA 02130
Work E:Mail:
[email protected]
Place of birth:
Rome, Italy
Work FAX: 617-264-5169
Education:
1982-1988
M.D. University of Rome “La Sapienza”, Rome, Italy
Postdoctoral Training:
Residencies:
1989-1993
Resident in Pathology, University of Rome “La Sapienza”
Fellowships:
1995-1996
1996-1997
Research Fellow in Hematopathology, Beth Israel Hospital, Boston,
MA
Research Fellow in Molecular Pathology, Beth Israel Deaconess
Medical Center, Boston MA.
Licensure and Certification:
1988
State licensure examination, Italy
Academic Appointments:
1996-1997
1999-2003
2003-2008
2009-
Research Fellow, Harvard Medical School, Boston, MA
Instructor in Pathology, Harvard Medical School
Assistant Professor of Pathology, Harvard Medical School
Associate Professor of Pathology, Harvard Medical School
Hospital Appointments:
1993-1995; 1998
1999-2003
1999-
Attending Pathologist, Istituto Dermopatico dell'Immacolata (IDI),
Rome, Italy
Research Associate, Brigham and Women’s Hospital
Associate Pathologist, Dana-Farber Cancer Institute
1
2003200620062011-
Associate Pathologist, Brigham and Women’s Hospital
Affiliate Faculty, Harvard Stem Cell Institute
Member, DFCI/BWH Center for Molecular Oncologic Pathology
Visiting Postdoctoral Scholar, Broad Institute of Harvard and MIT
Hospital and Health Care Organization Responsabilities:
1993-1995; 1998
1996-1997
1999-2004
2005-
Diagnostic Dermatopathology, Istituto Dermopatico
dell'Immacolata (IDI), Rome, Italy
Supervisor of the Core Molecular Pathology Laboratory at
Beth Israel Deaconess Medical Center
Associate Pathologist, Prostate Cancer Pathology Core Facility and In
situ Hybridization Core Facility, Dana-Farber Harvard Cancer Center
(DF/HCC)
Associate Pathologist, Specialized Histopathology Core Facility,
Dana-Farber Harvard Cancer Center (DF/HCC)
Major Administrative Responsibilities:
Local
200420082010-
Director, Tissue Acquisition Pathology and Clinical Data Core of
DF/HCC Kidney Cancer SPORE and Program
Director, DF/HCC Tissue Microarray and Imaging (TMI) Core
Co-Leader, DF/HCC Kidney Cancer Program
Major Committee Assignments:
Local
200420042005200520082008200920102011-
Member, DF/HCC Kidney Cancer SPORE Governance Committee
Co-chair, DF/HCC Kidney Cancer SPORE Specimens & Data
Utilization Committee
Member, DF/HCC Specialized Histopathology Core Facility User
Committee
Member, DF/HCC Tissue Microarray Core Facility User Committee
Member, DFCI/BWH Center for Molecular Oncologic Pathology
Advisory Committee
Member, DF/HCC Scientific Council
Member, Urologic Disease Working Group of The Cancer Genome
Atlas (TCGA) Program (NCI/ NHGRI)
Member, NCI Renal Cancer Task Force (RCTF)
Kidney Cancer Analysis Working Group of The Cancer Genome Atlas
(TCGA) Program (NCI/ NHGRI)
Professional Societies (Member):
1999-
American association for Cancer Research
New England Society of Pathologists
US and Canadian Academy of Pathology
2
Grant review activities:
2003
2004- 2005
2006-
Scientific Reviewer, Cell Biology Review Panel #1, Department of
Defense Prostate Cancer Research Program
Scientific Reviewer, Pathobiology Review Panel #3, Department of
Defense Prostate Cancer Research Program
Scientific Reviewer, Pathobiology Review Panel #2, Department of
Defense Prostate Cancer Research Program
Community Service Related to Professional Work:
2006; 2010
2007- 2009
Mentor, DF/HCC Continuing Umbrella of Research Experiences
(CURE) Program
Mentor, Partners Student Success Jobs Program, Brigham and
Women’s Hospital
Editorial activities:
2004-
Ad hoc reviewer:
American Journal of Pathology, American Journal of Physiology,
Breast Cancer Research, British Journal of Cancer, BJU International,
Cancer, Cancer Research, Clinical Cancer Research, Development,
Developmental Biology, Diagnostic Molecular Pathology, Human
Pathology, International Journal of Cancer, Journal of Urology,
Laboratory Investigation, Lancet Oncology, Nature Medicine, PLoS
ONE
2008-
Member, Editorial Board:
Clinical Cancer Research
Diagnostic Molecular Pathology
Awards and Honors:
1988
1998
2001
2002
2007
Part II
M.D, summa cum laude, University of Rome
The Daland Award, The New England Cancer Society, Worcester, MA
Hershey Young Investigator Award, Boston MA
CaP CURE Award
Partners in Excellence Award, Student Success Jobs Program Mentor
Research, Teaching, and Clinical Contribution
A. Narrative Report:
Research contributions: My research is focused on genitourinary malignancies, including
prostate, bladder and renal cancer.
Defining the cell(s) of origin of tumors is fundamental to elucidate the molecular mechanisms
involved in their pathogenesis. A major limitation for the identification of the cell type(s)
involved in the initiation and propagation of prostate and bladder cancers is that the identity of
stem cells and differentiation programs in these epithelia remains unclear. My research aims to
identify cell lineages in the prostate and bladder urothelium. I have previously demonstrated that
p63 is selectively expressed in basal cells of the prostate and urothelium and that p63-deficient
3
mice present defects in the development of these tissues. My subsequent studies have shown that
the early developing prostate (prostate buds) consists exclusively of p63-positive basal cells,
which then give rise to secretory cells and thus represent progenitor/stem cells. In contrast, my
analysis of the urothelium shows that umbrella (superficial) cells can develop and be maintained
independently from p63-positive cells. I am currently utilizing animal models to further
characterize the role of p63 in the development and renewal of the prostate and bladder
epithelium. This approach is likely to offer new insights in the biology of prostate and bladder
development and open new perspectives in the identification of the cell of origin of prostate and
bladder carcinoma.
An important focus of my research in kidney cancer is the identification of novel oncogenes and
tumor suppressor genes. In collaboration with Drs. Kaelin and Beroukhim at DFCI and the Broad
Institute, we are currently using an integrated analysis of single-nucleotide polymorphism (SNP)
arrays data with matched gene expression data to identify genes targeted by non-random genetic
aberrations in RCC. Results from these studies have the potential to identify new drug targets and
may eventually lead to new therapeutic approaches for patients with kidney cancer.
My laboratory is also very involved in translational research activities. I currently serve as the
Director of the Tissue Acquisition, Pathology, and Clinical Data (TAPCD) Core of the DF/HCC
Kidney Cancer SPORE and Program. I am also the Director of the DF/HCC Tissue Microaaray
and Imaging Core.
Teaching contributions: I have been actively involved in teaching since the beginning of my
career. I daily teach and tutor post-doctoral fellows and research assistant working in my research
laboratory. Moreover, I serve as a Tutor in the Pathology course at Harvard Medical School.
Clinical contributions: Throughout my career I have been involved in both patient care and in
the development of new tools that could be helpful in the diagnosis and treatment of diseases. As
a Research Fellow, I developed a novel PCR-based T-cell clonality assay, which is currently
being utilized for the diagnosis of T-cell lymphomas (Signoretti et al., Am J Pathol, 1999 and
accompanying editorial). More recently, I demonstrated that p63 is a reliable marker of prostate
basal cells that is not expressed in prostate carcinoma. After extensive validation by other
groups, p63 immunohistochemistry is currently used in routine clinical practice for the evaluation
of challenging prostate biopsies.
B. Funded Research Support:
Past
1996-1997
1997-1998
2001
Oncor, Inc. Evaluation of the Oncor HER-2/neu (ERBB2) gene
amplification detection kit for the interpahse detection of HER-2/neu
(ERBB2) genomic sequences in human breast tissue for node-negative
primary breast cancer. Multi-institutional study for FDA approval of
the HER-2/neu (ERBB2) gene amplification detection kit. (Kit FDA
approved Jan 1998). Co-investigator.
Ministero della Pubblica Istruzione, Rome, Italy. Detection of B-cell
clonality in cutaneous B-cell infiltrates. Co-investigator.
Hershey Foundation Award (Signoretti, DFCI). A mouse model for
prostate stem cells. Principal Investigator.
4
2001-2004
DOD U.S. Army, CDMRP - New Investigator Award (Signoretti,
DFCI). The basal cell marker p63 and prostate stem cells. Principal
Investigator.
2002
CaP CURE Foundation Award (Signoretti, DFCI). An animal model
for the identification of prostate stem cells. Principal Investigator.
2002-2007
NIH/NCI. Prostate Cancer SPORE / Pathology Core (Kantoff, DFCI).
Co-investigator.
2004-2006
NIH/NCI. Kidney Cancer SPORE Developmental Project (Signoretti,
BWH). Molecular analysis of renal cell carcinoma using Single
Nucleotide Polymorphisms (SNP) arrays. Principal Investigator.
2005-2007
NIH/NIDDK-R21. Defining cell lineages in the bladder urothelium
(Signoretti, BWH). Principal Investigator.
2006-2008
NIH/NCI.
Kidney Cancer SPORE Developmental Project.
Development of mouse orthotopic xenografts of human renal cell
carcinoma (Signoretti, BWH). Principal Investigator.
02/08/06-02/07/10
DOD. U.S. Army. CDMRP - Idea Development Award. p63 in
development and maintenance of the prostate epithelium (Signoretti,
BWH). Principal Investigator.
2007
NIH/NCI. ICBP Pilot Project supported by 5U54 CA112962-03
(Golub, DFCI). Integrating gene expression with high-resolution
genetic analysis to identify oncogenic kinases in kidney cancer.
Principal Investigator.
01/01/07-12/31/08
Doris Duke Charitable Foundation. Distinguished Clinical Scientist
Award (Kaelin, DFCI). Co-investigator.
06/01/07-06/30/09
Harvard Stem Cell Institute. Seed Grant. Identification of Stem Cells
In Prostate and Bladder Epithelia (Signoretti, BWH). Principal
Investigator.
09/01/09 – 08/31/10 NIH/NCI. of the Kidney Cancer SPORE P50 CA101942 Developmental Project.
Clinical, histological and molecular
determinants of bilateral renal cell cancer. Principal Investigator.
Current
Active
04/01/01-03/31/11
05/19/06-11/30/11
05/19/06-11/30/11
06/01/09-05/31/14
NIH/NCI. PO1 CA089021. The Role of PTEN and PI3K Pathway in
Prostate Cancer (Cantley, BIDMC). Co-investigator.
NIH/NCI. DF/HCC P30 CA06516. Specialized Histopathology Core
(Aster, BWH). Co-investigator.
NIH/NCI. DF/HCC P30 CA06516. Tissue Microarray and Imaging
(TMI) Core (Signoretti, BWH). Principal Investigator.
NIH/NCI. Kidney Cancer SPORE P50 CA101942. Tissue Acquisition
Pathology and Clinical Data Core (CORE# 3) (Signoretti, BWH).
Principal Investigator.
5
06/01/09-05/31/14
NIH/NCI. Kidney Cancer SPORE P50 CA101942. Treatment of
VHL-/- clear cell renal carcinoma with HIF2 siRNA (Kaelin DFCI,
Choueiri DFCI, Signoretti BWH). Co-Principal Investigator of
Project 2.
09/01/10 – 07/31/15 NIH/NIDDK. 1R01DK089975 (Signoretti, BWH). Mechanisms
Regulating Prostate Epithelium Maintenance and Regeneration.
Principal Investigator.
04/01/11-03/31/15
NIH/NCI. 1R01 CA152330-01 (Seth, BIDMC). Pathway Specific
Imaging in VHL Deficient Renal Cancer. Co-investigator.
11/01/11-10/30/15
NIH/NCI. 1R01CA154475-01 (Pedrosa, BIDMC). Non-invasive
Physiologic Predictors of Aggressiveness in Renal Cell Carcinoma.
Co-investigator.
11/01/11-10/30/12
NIH/NCI. Kidney Cancer SPORE P50 CA101942. Director’s choice
Award. Characterization of molecular alterations in metanephric
adenoma of the kidney. Principal Investigator.
C. Current Research Activities
#1: Role of p63 in development and renewal of the prostate and bladder epithelium
Unraveling the mechanisms regulating the development and renewal of normal tissues is not only
one of the main goals of developmental biology but also an essential step for the elucidation of
the mechanisms underlying the development of pathological processes, namely cancer. Although
epithelial stem cells have been identified in the skin and intestine, the way the prostate and
bladder epithelium are formed and maintained remains unclear.
The basal cell marker p63 is selectively expressed in the basal cells of several epithelia, including
the prostate and the bladder. My research group has previously demonstrated that p63-deficient
(p63-/-) mice present defects in prostate buds and urothelial development (Signoretti et al., Am J
Pathol 2000). We have more recently performed in vivo studies utilizing the p63-/- mouse as a
tool to define cell lineages in the prostate epithelium and urothelium. Results from these studies
show that when developmental defects of p63-/- embryos are abolished by injecting p63+/+ ES
cells into 3.5dpc p63-/- blastocysts, only p63+/+ cells compose the normal prostate epithelium of
7-weeks old chimeric mice. These findings indicate that prostate secretory cells of young adult
mice derive from p63-positive progenitor cells that constitute the prostate buds. Surprisingly, in
contrast with the prostate findings, analysis of the urothelium of the rescued p63-/- chimeras
demonstrates that urothelial umbrella cells can develop independently from p63-positive basal
and intermediate cells (Signoretti et al, Proc Natl Acad Sci U S A 2005).
My current research aims at further defining stem cells and differentiation programs in the adult
prostate and bladder epithelia. Specifically, we are performing genetic lineage tracing
experiments to directly follow the fate of p63-positive cells in the prostate and bladder epithelia
in vivo.
The secondary goal of this endeavor is to identify molecular mechanisms mediating p63 function
during both development and tumorogenesis. We have shown that prostate basal cells
predominantly express the Np63 isosform and that Np63 is required for cell survival.
Importantly, we have also demonstrated that Fatty Acid Synthase (FASN) is a functionally
6
relevant target of p63 and is required for mediating its pro-survival effects (Sabbisetti, PLoS
ONE, 2009). Our results establish a novel functional link between this p53 family member and
lipid metabolism and suggest that maintenance of fatty acid synthesis is a key mechanism
through which p63 acts as a pro-survival molecule in both development and cancer.
Research #2: Molecular Analysis Of Renal Cell Carcinoma Using Single Nucleotide
Polymorphisms (SNP) Arrays
Clear cell renal cell carcinoma (cRCC) represents the most common and fatal form of renal
cancer and accounts for 70-80% of cases. In patients with advanced disease, response rates to
traditional chemotherapy and radiotherapy are, unfortunately, very low. The introduction of
cytokine-based immunotherapy with interferon- or interleukin-2 for patients with metastatic
disease has shown survival improvements, but the treatment is often not well tolerated and only a
limited subset of patients experience clinically meaningful benefit. Recently, tyrosine kinase
inhibitors (TKIs) that target the VHL pathway, including sorafenib and sunitinib, have shown
clear activity in metastatic cRCC and have received approval by the FDA. However, not all the
patients treated with these targeted therapies experience a substantial clinical benefit and almost
all of them eventually progress. Therefore, more effective treatments for cRCC are warranted.
Kinases are tractable therapeutic targets with multiple small molecule inhibitors in development.
Identification of new kinases that play an important role in the development and progression of
cRCC would enable rapid development of more effective therapeutic approaches. Highthroughput genetic studies represent a unique opportunity to identify the tumor suppressor genes
(TSGs) and oncogenes, including kinases, upon which genetic subtypes of cRCC depend. Highresolution single nucleotide polymorphism (SNP) arrays are able simultaneously to delineate
regions of copy-number gain and loss and loss-of-heterozygosity (LOH) at high resolution
throughout the genome. In collaboration with Drs. Kaelin and Beroukhim at DFCI and the Broad
Institute, we are currently performing integrated analysis of SNP array data describing
chromosomal aberrations with matched gene expression data to identify candidate kinases
targeted by these aberrations in cRCC (Beroukhim et al, Cancer Res, 2009). Results from these
studies will shed light on the molecular mechanisms underlying kidney cancer development and
might eventually lead to more effective targeted therapies for this disease.
D. Report of Teaching:
1. Local contributions
Medical School Teaching
1995; 1998
1997
1998
Resident teaching: daily training of pathology Residents from
University of Rome “la Sapienza”, rotating through the Pathology
Service of Istituto Dermopatico dell’Immacolata. 4 Residents per year.
Preparation and contact time: 1-3 hours/day.
Resident teaching: Clinical Pathology rotation (of one month duration)
in the Molecular Pathology Laboratory at Beth Israel Deaconess
Medical Center. 6 Residents per year. Preparation and contact time: 510 hours/week.
Istituto Dermopatico dell’Immacolata, Rome, Italy. Basic course in
dermatopathology for Pathologists and Dermatologists. Lecturer. 10-
7
1999-2003
2001-2007
15 Post-doctoral Fellows. Duration of the course: 1 week. Preparation
and contact time: 3 hours/day.
Teaching and supervising of rotating Genetic Pathology Fellows from
the Department of Pathology, Brigham and Women’s Hospital,
Boston. 1 Post-doctoral Fellow per year. Duration of the rotation: 1
month. Preparation and contact time: 6-8 hours/week
Pathology course, Harvard Medical School (course director: Dr.
Andrew Lichtman), Tutor. 8-10 Medical Students. Preparation and
contact time: 8-10 hours for each tutorial.
Local Invited Teaching Presentations
2000
2002
2005
2005
2005
2006
2006
2007
2008
2009
2009
2009
2009
2010
2010
Dana-Farber Cancer Institute. Seminars in Genitourinary Oncology.
Invited speaker: “p63 is a prostate basal cell marker and is required for
prostate development”.
Dana-Farber Cancer Institute. Seminars in Genitourinary
Oncology. Invited speaker: “p63 and prostate stem cells”.
Dana-Farber Cancer Institute. Seminars in Cancer Genomics. Invited
Speaker: “Role of the F-box protein Skp2 in human breast cancer”.
DF/HCC Kidney Cancer Program Meeting. Invited Speaker:
“Molecular analysis of renal cell carcinoma using single nucleotide
polymorphisms (SNP) arrays”.
Brigham and Women’s Hospital. Thorn 5/6 Seminar Series. Invited
Speaker: “p63 and Prostate Development”.
DF/HCC Kidney Cancer Program Meeting. Invited Speaker:
“Genome-wide analysis of genetic alterations in clear cell carcinoma
of the kidney”.
Beth Israel Deaconess Medical Center. GU Data Club. Invited
Speaker. “p63 in genitourinary development”.
DF/HCC Kidney Cancer Program Meeting. Invited Speaker:
“Development of Clinically Relevant Mouse Orthotopic Xenografts of
Human Renal Cell Carcinoma”.
DF/HCC Kidney Cancer Program Meeting. Invited Speaker:
“Mouse Orthotopic Xenografts of Human Renal Cell Carcinoma”.
Harvard Urology and Prostate Cancer Research Seminar Series.
Invited Speaker: “p63 and Prostate Cell Lineages”.
Brigham and Women’s Hospital. Thorn 5/6 Seminar Series. Invited
Speaker: “Non-Random Genetic Abnormalities in Kidney Cancer”
Dana-Farber Cancer Institute. Seminars in Genitourinary Oncology.
Invited speaker: “Defining cell lineages in the prostate epithelium”.
Harvard Stem Cell Institute Retreat. Invited speaker:
“Identification of stem cells in prostate and bladder epithelia”.
Brigham and Women’s Hospital. Surgical Pathology Updates Seminar
Series. Invited Speaker: “Molecular Pathology of Kidney Cancer”.
Brigham and Women’s Hospital. Thorn 5/6 Seminar Series. Invited
Speaker: “Molecular Characterization of Kidney Cancer”
8
2011
2011 DF/HCC Kidney Cancer Program Retreat. Invited Speaker:
“Orthotopic Xenografts of RCC retain histological, immunophenotypic
and genetic features of tumors in patients”.
Continuing Medical Education
2006
Harvard Medical School, Department of Continuing Education.
Regional Renal Cancer Symposium: Recent Advances in the Biology
and Treatment of Renal Cell Carcinoma. Invited Speaker: “Renal
Cancer Pathology and Tissue Banking”.
Advisory And Supervisory Responsibilities In Laboratory Setting
20032006; 2010
2007-2009
Supervising research activities of Post-doctoral Fellows and College
Graduates. 30 hours/week
Mentor. The DF/HCC Continuing Umbrella of Research Experiences
(CURE) Program. 6 hours/week
Mentor. Brigham and Women’s Hospital Student Success Jobs
Program. 6 hours/week
2. Regional, National and International Contributions
Regional presentations
1997
1998
1998
2007
University of Rome, Rome, Italy. Invited lecture: “Antigen receptor
genes analysis in the diagnosis of cutaneous.lymphomas”.
Istituto Dermopatico dell’Immacolata, Rome, Italy. Continuing
medical education course: “Melanocytic nevi: histological features”.
Istituto Dermopatico dell’Immacolata, Rome, Italy. Invited lecture:
“Detection of clonal T-cell receptor  gene rearrangements by PCRSSCP analysis”.
University of Massachusetts Medical School, Genitourinary Program
Seminars. Invited lecture: “p63 in genitourinary development”.
National presentations
2002
2006
2006
2006
2006
Prouts Neck Prostate Cancer Meeting. Invited lecture: The basal cell
marker p63 and prostate stem cells.
14th Annual SPORE Investigators’ Workshop, GU (Renal) Breakout
Session. Invited lecture: “Predictive markers for response to CCI-779,
IL-2, and sorafenib”.
2006 AUA/SBUR Summer Research Conference. Invited lecture: “p63
in bladder development”.
Basic Research in Interstitial Cystitis: Second Investigators’ Meeting
(NIH/NIDDK). Guest Speaker. “p63 in the development of the
urothelium”.
NCI-Sponsored Renal Cancer Biomarkers Workshop. Organizer and
Invited Speaker. “Preparation and use of RCC Tissue Microarrays”.
9
2007
2008
15th Annual SPORE Investigators’ Workshop, GU (Renal) Breakout
Session. Invited lecture: “Report on the NCI-Sponsored Renal Cancer
Biomarkers Workshop”.
Cambridge Conference on Innovations and Challenges in Renal
Cancer. Invited lecture: “Tissue Biomarkers in Renal Cell Carcinoma:
Issues and Solutions"
International presentations
2000
2004
2006
2007
2008
2009
International Academy of Pathology, Alghero, Italy. Invited lecture:
“The use of laser capture microdissection (LCM) in molecular
pathology”.
5th World Congress on Urological Research, London, UK. Invited
lecture: “Defining progenitor cells in the prostate epithelium”.
The Kidney Cancer Association’s Fifth International Kidney Cancer
Symposium. Invited lecture: “Predictive markers of response to
therapy for advanced renal cancer”.
CAIX Symposium- Brussels, Belgium. Invited lecture: “CAIX
Expression as a Biomarker in Renal Cancer”.
2008 Prostate Cancer Research Foundation Forum, Toronto, Canada.
Invited lecture: “Lineage commitment in prostate development”.
2009 ASCO Annual Meeting, Orlando, FL. Invited lecture: “Tumor
biology to predict response and resistance in renal carcinoma”.
E. Report of clinical activities:
1. Field:
Dermatopathology. Teaching hospital: Staff pathologist, Istituto
Dermopatico dell’Immacolata (1993-1995; 1998).
2. Patient load:
30,000 surgical pathology cases/year (1993-1995; 1998). 500
molecular diagnostic cases/year (1996-1997).
3. Clinical contributions:
1998
2000
Development of a PCR-based methodology for TCR gene
rearrangement analysis in paraffin-embedded tissue, extensively used
in routine clinical practice.
Identification of p63 as a reliable marker of prostate basal cells that is
not expressed in prostate carcinoma. p63 immunohistochemistry is
currently used in routine clinical practice for the diagnosis of
challenging prostate biopsies.
10
Part III
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8. Ascoli V, Nardi F, Carnovale Scalzo C, Signoretti S, Pistilli A, Lo Coco F. Absence of
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11
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transcription factors are critical effectors of cell death and cell cycle arrest downstream of
PTEN. Mol Cell Biol. 2000;20:8969-82.
21. Ascoli V, Signoretti S, Onetti Muda A, Della Rocca C, Mastroianni C M, Gastaldi R,
Pescarmona E, Nardi F, Gaidiana G, Carbone A, Lo Coco F. Primary effusion lymphoma in
HIV-infected patients with multicentric Castleman’s disease. J Pathol. 2001;193:200-9.
22. Datta MW, Macri’ E, Signoretti S, Renshaw A A, Loda M. Transition from in situ to
invasive testicular germ cell neoplasia is characterized by the loss of p21 and gain of mdm-2
expression. Mod Pathol. 2001;14:437-42.
23. Waltregny D, Leav I, Signoretti S, Soung P, Lin D, Merk F, Adam YA, Bhattacharya N,
Cirenei N, Loda M. Androgen-driven prostate epithelial cell proliferation and differentiation
in vivo involve the regulation of p27 kip1 through its proteasome-mediated degradation. Mol
Endocrinol. 2001;15:765-82.
24. Di Rienzo J, Signoretti S, Nakamura N, Rivera-Gonzales R, Sellers WR, Loda M, Brown M.
Growth factor requirement and basal phenotype of immortalized mammary epithelial cells.
Cancer Res. 2002 Jan 1;62(1):89-98.
25. Bardeesy N, Morgan J, Sinha M, Signoretti S, Srivastava S, Loda M, Merlino G, DePinho
RA. Obligate role for p16Ink4a and p19arf-p53 in murine pancreatic neoplasia. Mol Cell Biol.
2002;22:635-43.
26. Lindeman N, Waltregny D, Signoretti S, Loda M. Gene transcript quantitation by real time
RT-PCR in cells selected by immunohistochemistry-laser capture microdissection. Diag Mol
Pathol. 2002;4:187-92.
27. Gounari F, Signoretti S, Klein L, Bronson R, Sellers WR, Kum J, Siermann A, Taketo MM,
von Boehmer H, Khazaie K. Stabilization of -Catenin induces prostatic intraepithalial
12
neoplasia, but terminal squamous transdifferetiation of other secretory epithelia. Oncogene.
2002;21:4099-107.
28. Signoretti S, di Marcotullio L, Richardson A, Ramaswamy S, Carrano A C, Isaac B, Rue M,
Monti F, Loda M and Pagano M. Oncogenic role of the ubiquitin ligase subunit Skp2 in
human breast cancer. J Clin Invest. 2002;110:633-41.
29. Bardeesy N, Sinha M, Hezel A F, Signoretti S, Hathaway N A, Sharpless N E, Loda M,
Carrasco D R and DePinho RA. Loss of the Lkb1 tumor suppressor provokes intestinal
polyposis but resistance to transformation. Nature. 2002;419:162-7.
30. Weinstein MH, Signoretti S, Loda M. Diagnostic utility of immunohistochemical staining
for p63, a sensitive marker of prostatic basal cells. Mod Pathol. 2002;12:1302-1308.
31. Garraway LA, Lin D, Signoretti S, Waltregny D, Dilks J, Bhattacharya N, Loda M.
Intermediate Basal Cells of the Prostate: In Vitro and In Vivo Characterization. Prostate.
2003;15:206-18.
32. Graner E, Tang D, Rossi S, Baron A, Migita T, Weinstein LJ, Lechpammer M, Huesken D,
Zimmermeann J, Signoretti S, Loda M. The isopeptidase USP2a regulates the stability of
Fatty Acid Synthase in prostate cancer. Cancer Cell. 2004; 5:253-61.
33. Murphy M, Carlson JA, Keough MP, Claffey KP, Signoretti S, Loda M. Hypoxia regulation
of the cell cycle in malignant melanoma: putative role for the cyclin dependent kinase
inhibitor p27. J Cutan Pathol. 2004;31:477-82.
34. Berger R, Febbo PG, Majumder PK , Zhao J, Mukherjee S, Signoretti S, Campbell KT,
Sellers WR, Roberts TM, Loda M, Golub TR, Hahn WC. Androgen-induced differentiation
and tumorigenicity of human prostate epithelial cells. Cancer Res. 2004; 64:8867-75.
35. Horkan C, Dalal K, Coderre JA, Kiger JL, Dupuy DE, Signoretti S, Goldberg SN. Tumor
ablation: reduced tumor growth with combined radiofrequency ablation and radiation therapy
in a rat breast tumor model. Radiology. 2005;235(1):81-8.
36. Atkins MB, Regan M, McDermott D, Mier J, Stanbridge E, Youmans A, Febbo P, Upton M,
Lechpammer M, Signoretti S. Carbonic Anhydrase IX Expression Predicts Outcome of IL-2
Therapy. Clin Cancer Res. 2005; 11:3714-21.
37. Zea AH, Rodriguez PC, Atkins MB, Hernandez C, Zabaleta J, Quiceno D, Signoretti S,
McDermott D, Youmans A, O’Neill A, Regan M, Mier J, Ochoa AC. Suppressor Myeloid
Cells in Renal Cell Carcinoma Block T Cell Function and z Chain Expression. Cancer Res.
2005; 65:3044-8.
38. Ahmed M, Liu Z, Lukyanov AN, Signoretti S, Horkan C, Monsky WL, Torchilin VP,
Goldberg SN. Combination radiofrequency ablation with intratumoral liposomal
doxorubicin: effect on drug accumulation and coagulation in multiple tissues and tumor types
in animals. Radiology. 2005; 235:469-77.
39. Luo J, Sobkiw CL, Logsdon NM, Watt JM, Signoretti S, O'connell F, Shin E, Shim Y, Pao
L, Neel BG, Depinho RA, Loda M, Cantley LC. Modulation of epithelial neoplasia and
lymphoid hyperplasia in PTEN+/- mice by the p85 regulatory subunits of phosphoinositide 3kinase. Proc Natl Acad Sci (U S A). 2005; 102:10238-43.
13
40. Signoretti S*, Pires MM, Lindauer M, Horner JW, Grisanzio C, Dhar S, Majumder P,
McKeon F, Kantoff PW, Sellers WR, Loda M*. p63 regulates commitment to the epithelial
cell lineage. Proc Natl Acad Sci (U S A). 2005; 102:11355-60.
41. De Marzo AM, Platz EA, Epstein JI, Ali T, Billis A, Chan TY, Cheng L, Datta M, Egevad L,
Ertoy-Baydar D, Farre X, Fine SW, Iczkowski K A, Ittmann M, Knudsen S, Loda M, LopezBeltran A, Magi-Galluzzi C, Mikuz G, Montironi R, Pikarsky E, Pizov G, Rubin M A,
Samaratunga H, Sebo T, Sesterhenn IA, Shah RB, Signoretti S, Simko J, Thomas G,
Troncoso P, Tsuzuki TT, van Leenders GJ, Yang XJ, Zhou M, Figg WD, Hoque A and Lucia
MS. A working group classification of focal prostate atrophy lesions. Am J Surg Pathol.
2006; 30(10):1281-91.
42. Berger R, Lin DI, Nieto, Sicinska Ewa, L. Garraway LA, Heiner A, Signoretti S, Hahn WC
and Loda M. Androgen-dependent regulation of Her-2/neu In Prostate Cancer Cells. Cancer
Res. 2006; 66:5723-8.
43. Hines-Peralta A, Sukhatme V, Regan M, Signoretti S, Liu ZJ, Goldberg SN. Improved
Tumor Destruction with Arsenic Trioxide and Radiofrequency Ablation in Three Animal
Models. Radiology. 2006; 240(1):82-9.
44. Hakime A, Hines-Peralta A, Peddi H,. Atkins MB, Sukhatme VP, Signoretti S, Regan M,
and Goldberg SN. Combination of radiofrequency with antiagiogenic therapy increases tumor
ablation efficacy. Radiology. 2007; 244(2):464-70.
45. Zhan Q, Signoretti S, Whitaker-Menezes D, Friedman TM, Korngold R and Murphy GF.
Cytokeratin15-Positive Basal Epithelial Cells Targeted in Graft-Versus-Host Disease Express
a Constitutive Antiapoptotic Phenotype. J Invest Dermatol. 2006; 27(1):106-15.
46. Thomas RK, Baker AC, Debiasi RM, Winckler W, Laframboise T, Lin WM, Wang M, Feng
W, Zander T, Macconnaill LE, Lee JC, Nicoletti R, Hatton C, Goyette M, Girard L,
Majmudar K, Ziaugra L, Wong KK, Gabriel S, Beroukhim R, Peyton M, Barretina J, Dutt A,
Emery C, Greulich H, Shah K, Sasaki H, Gazdar A, Minna J, Armstrong SA, Mellinghoff IK,
Hodi FS, Dranoff G, Mischel PS, Cloughesy TF, Nelson SF, Liau LM, Mertz K, Rubin MA,
Moch H, Loda M, Catalona W, Fletcher J, Signoretti S, Kaye F, Anderson KC, Demetri GD,
Dummer R,Wagner S, Herlyn M, Sellers WR, Meyerson M, Garraway LA. High-throughput
oncogene mutation profiling in human cancer. Nat Genet. 2007; 39(3):347-51.
47. Cho D, Signoretti S, Dabora S, Regan M, Seeley A, Mariotti M, Youmans A,
Polivy A, Mandato L, McDermott D, Stanbridge E, Atkins M. Potential
histologic
and
molecular
predictors
of
response
to
temsirolimus
in
patients with advanced renal cell carcinoma.
Clin Genitourin Cancer.
2007;5(6):379-85.
48. Sabir A, Schor-Bardach R, Wilcox CJ, Rahmanuddin S, Atkins MB, Kruskal JB, Signoretti
S, Raptopoulos VD, Goldberg SN. Perfusion MDCT enables early detection of therapeutic
response to antiangiogenic therapy. AJR Am J Roentgenol. 2008 Jul;191(1):133-9.
49. Young AP, Schlisio S, Minamishima YA, Zhang Q, Li L, Grisanzio C, Signoretti S, Kaelin
WG Jr. Acute Loss of pVHL Actuates a HIF-independent Senescence Program Mediated by
pRb and p400. Nat Cell Biol. 2008; 10(3):361-9.
14
50. Jia S, Liu Z, Zhang S, Liu P, Zhang L, Lee SH, Zhang J, Signoretti S, Loda M, Roberts TM,
and Zhao JJ. Kinase-dependent and -independent roles of PI3K-p110β in cell growth,
metabolism and tumorigenesis. Nature. 2008;454(7205):776-9.
51. Majumder P, Grisanzio C, O’Connell F, Xu Q, Berger R, Herman P, Bikoff R, Baek WK,
Wang S, Ellwood-Yen K, Hahn WC, Wu H, Sawyers CL, Signoretti S, Loda M, Sellers WR.
A prostatic intraepithelial neoplasia-dependent p27kip1 checkpoint induces senescence,
inhibits cell proliferation and cancer progression. Cancer Cell. 2008;14(2):146-55.
52. Hulick P, Zimmer M, Margulis V, Skates S, Hamel M, Dahl M. D, Michaelson D,
Liebermann T, Signoretti S, Carney W, Wood C, Iliopoulos O. Blood Levels of Carbonic
Anhydrase 9 Correlate with Clear Cell Renal Cell Carcinoma Activity. Clin Proteom. 2009;
5:37-45.
53. Xie H, Valera VA, Merino MJ, Amato AM, Signoretti S, Linehan WM, Sukhatme VP, Seth
P. LDH-A Inhibition, a therapeutic strategy for treatment of Hereditary Leiomyomatosis and
Renal Cell Cancer (HLRCC). Mol Cancer Ther. 2009;8(3):626-35.
54. Migita T, Ruiz S, Fornari A, Inazuka F, Fiorentino M, Zadra G, Grisanzio C, Palescandolo E,
Priolo C, Shin E, Fiore C, Xie W, Kung A, Febbo P, Subramanian A, Mucci L, Ma J,
Signoretti S, Stampfer M, Hahn W, Finn S, Loda M. Fatty Acid Synthase: A Metabolic
Enzyme and Candidate Oncogene in Prostate Cancer. J Natl Cancer Inst. 2009;101(7):51932.
55. Walker SR, Nelson EA, Zou L, Chaudhury M, Signoretti S, Richardson A, Frank DA.
Reciprocal effects of STAT5 and STAT3 in breast cancer. Mol Cancer Res. 2009 Jun 2.
[Epub ahead of print].
56. Wiklund F, Tretli S, Choueiri TK, Signoretti S, Fall K, Adami HO. The risk of bilateral
renal cell cancer. J Clin Oncol. 2009;27:3737-41.
57. Schor-Bardach R, Alsop DC, Pedrosa I, Solazzo SA, Wang X, Marquis RP, Atkins MB,
Regan M, Signoretti S, Lenkinski RE, Goldberg SN. Does Arterial Spin-labeling MR
Imaging–Measured Tumor Perfusion Correlate with Renal Cell Cancer Response to
Antiangiogenic Therapy in a Mouse Model? Radiology. 2009;251(3):731-42.
58. Beroukhim R, Brunet JP, Di Napoli A, Mertz KD, Seeley A, Pires MM, Linhart D, Worrell
RA, Moch H, Rubin, RA, Sellers WR, Meyerson M, W Linehan M, Rubin M, Kaelin WG,
Signoretti S. Patterns of gene expression and copy-number alterations in VHL diseaseassociated and sporadic clear cell carcinoma of the kidney. Cancer Res. 2009;69(11):467481.
59. Sabbisetti S, Di Napoli A, Seeley A, Amato AM, O’Regan E, Ghebremichael M, Loda M,
Signoretti S. p63 Promotes Cell Survival Through Fatty Acid Synthase. PLoS ONE.
2009;4(6):e5877.
60. Solazzo SA, Ahmed M, Schor-Bardach R, Yang W, Girnun GD, Rahmanuddin S, Levchenko
T, Signoretti S, Spitz DR, Torchilin V, Goldberg SN. Liposomal Doxorubicin Increases
Radiofrequency Ablation-induced Tumor Destruction by Increasing Cellular Oxidative and
Nitrative Stress and Accelerating Apoptotic Pathways. Radiology. 2010 255(1):62-74.
15
61. Beroukhim R, Mermel CH, Porter D, Wei G, Raychaudhuri S, Donovan J, Barretina J,
Boehm JS, Dobson J, Urashima M, McHenry K, Pinchback R, Ligon AH, Cho J, Haery L,
Greulich H, Reich M, Winckler W, Weir BA, Tanaka K, Chiang DY, Bass AJ, Loo A,
Hoffman C, Prensner J, Liefeld T, Yecies D, Signoretti S, Maher E, Kaye FJ, Sasaki H,
Tepper JE, Fletcher JA, Baselga J, Tsao M, Rubin MA, Janne PA, Daly MJ, Nucera C,
Levine RL, Ebert BL, Gabriel S, Rustgi AK, Antonescu CR, Ladanyi M, Letai A, Garraway
LA, Loda M, Beer DG, True LD, Okamoto A, Pomeroy SL, Singer S, Lander ES, Getz G,
Golub TR, Sellers WR, Meyerson M. The landscape of copy number alterations across
multiple human cancers. Nature. 2010;463:899-905.
62. Choueiri TK, Regan MM, Rosenberg JE, Oh WK, Clement J, Amato AM, McDermott D,
Cho DC, Atkins MB, Signoretti S. Carbonic anhydrase IX (CAIX) and pathologic features as
predictors of outcome in patients with metastatic clear-cell renal cell carcinoma receiving
VEGF-targeted therapy. BJU Int. 2010;106(6):772-8.
63. Lee SH, Poulogiannis G, Pyne S, Jia S, Zou L, Signoretti S, Loda M, Cantley LC, and
Roberts TM. A constitutively activated form of the p110β isoform of PI3-kinase induces
prostatic intraepithelial neoplasia in mice. Proc Natl Acad Sci (U S A). 2010;107(24):110027.
64. Cho DC, Cohen MB, Panka DJ, Collins M, Ghebremichael M, Atkins MB, Signoretti S,
Mier JW. The Efficacy of the Novel Dual PI3-Kinase/mTOR Inhibitor NVP-BEZ235
Compared to Rapamycin in Renal Cell Carcinoma. Clin Cancer Res. 2010;16(14):3628-38.
65. Yang W, Ahmed M, Elian M, Hady ES, Levchenko TS, Sawant RR, Signoretti S, Collins M,
Torchilin VP, Goldberg SN. Do Liposomal Apoptotic Enhancers IncreaseTumor Coagulation
and End-Point Survival in Percutaneous Radiofrequency Ablation of Tumors in a Rat Tumor
Model? Radiology 2010 Sep 21. [Epub ahead of print].
66. Genega, EM, Ghebremichael, M, Najarian R, Fu Y, Wang, Y, Argani, P, Grisanzio, C,
Signoretti S. CAIX Expression in Renal Neoplasms: Correlation with Tumor Type and
Grade. Am J Clin Pathol. 2010;134(6):873-9.
67. Bhatt R, Wang X, Zhang L, Collins M, Signoretti S, Alsop D, Goldberg SN, Atkins MB,
Mier JW. Renal cancer resistance to antiangiogenic therapy is delayed by restoration of
angiostatic signaling. Mol Cancer Ther. 2010:9(10):2793-802.
68. Moslehi J, Minamishima YA, Padera RF, Signoretti S, Liao R, and Kaelin WG. Loss of
PHD Prolyl Hydroxylase Activity in Cardiomyocytes Phenocopies Ischemic
Cardiomyopathy. Circulation. 2010;122(10):1004-16.
69. Gan B, Lim C, Chu G, Hua S, Ding Z,Collins M, Hu J, Jiang S, Fletcher-Sananikone E,
Zhuang L, Chang M, Zheng H, Wang YA, Kwiatkowski DJ, Kaelin WG, Signoretti S and
DePinho RA. FoxOs enforce a progression checkpoint to constrain mTORC1-activated renal
tumorigenesis. Cancer Cell. 2010;18(5):472-84.
70. Ding Z, Wu C, Chu GC, Xiao Y, Ho D, Zhang J, Perry SR, Labrot ES, Wu X, Lis R, Hoshida
Y, Hiller D, Hu B, Jiang S, Zheng H, Stegh AH, Scott AL, Signoretti S, El-Bardeesy NM,
Wang YA, Hill D, Golub TR, Stampfer MJ, Wong WH, Loda M, Mucci L, Chin L &
16
DePinho RA. SMAD4-dependent barrier constrains prostate cancer growth and metastatic
progression. Nature. 2011;470(7333):269-73.
71. Bernardi R, Papa A, Egia A, Coltella N, Teruya-Feldstein J, Signoretti S and Pandolfi PP.
Pml represses tumor progression through inhibition of mTOR. EMBO Mol Med.
2011;3(5):249-57.
72. Flavin R, Finn SP, Choueiri TK, Ingoldsby H, Ring M, Barrett C, Rogers M, Smyth P,
O'Regan E, Gaffney E, O'Leary JJ, Loda M, Signoretti S, Sheils O. RET protein expression
in papillary renal cell carcinoma. Urol Oncol. 2011 Mar 9. [Epub ahead of print].
73. Lee SH, Jia S, Zhu Y, Utermark T, Signoretti S, Loda M, Schaffhausen B, Roberts TM.
Transgenic expression of polyoma virus middle T antigen in the mouse prostate gives rise to
carcinoma. J Virol. 2011;85(11):5581-92.
74. Zhang L, Bhasin M, Schor-Bardach; R, Wang X, Collins MP, Panka D, Putheti P, Signoretti
S, Alsop DC, Libermann T, Atkins MB, Mier JW, Goldberg NS, Bhatt RS. Resistance of
renal cell carcinoma to sorafenib is mediated by potentially reversible gene expression. PLoS
ONE. 2011;6(4):e19144.
75. Grisanzio C, Seeley A, Chang M, Collins M, Di Napoli A, Cheng SC, Percy A, Beroukhim
R, Signoretti S. Orthotopic xenografts of RCC retain histological, immunophenotypic and
genetic features of tumors in patients. J Pathol. 2011 May 2. [Epub ahead of print].
76. Shen C, Beroukhim R, Schumacher S, Zhou J, Chang M, Signoretti S, and Kaelin WG.
Genetic and Functional Studies Implicate HIF1alpha as a 14q Kidney Cancer Suppressor
Gene. Cancer Discovery. 2011;1:222-235
77. Lin W, Cao J, Liu J, Beshiri ML, Fujiwara Y, Francis J, Cherniack AD, Geisen C, Blair LP,
Zou MR, Shen X, Kawamori D, Liu Z, Grisanzio C, Watanabe H, Minamishima YA, Zhang
Q, Kulkarni RN, Signoretti S, Rodig SJ, Bronson RT, Orkin SH, Tuck DP, Benevolenskaya
EV, Meyerson M, Kaelin WG, and Yan Q. Loss of the RBP2 histone demethylase suppresses
tumorigenesis in mice lacking Rb1 or Men1. Proc Natl Acad Sci (U S A). 2011;108:1337986.
78. Yang W, Ahmed M, Tasawwar B, Levchenko T, Sawant RR, Collins M, Signoretti S,
Torchilin V, Goldberg SN. Radiofrequency ablation combined with liposomal quercetin to
increase tumour destruction by modulation of heat shock protein production in a small animal
model. Int J Hyperthermia. 2011;27(6):527-38.
79. Bass AJ, Lawrence MS, Brace LE, Ramos AH, Drier Y, Cibulskis K, Sougnez C, Voet D,
Saksena G, Sivachenko A, Jing R, Parkin M, Pugh T, Verhaak RG, Stransky N, Boutin AT,
Barretina J, Solit DB, Vakiani E, Shao W, Mishina Y, Warmuth M, Jimenez J, Chiang DY,
Signoretti S, Kaelin WG, Spardy N, Hahn WC, Hoshida Y, Ogino S, Depinho RA, Chin L,
Garraway LA, Fuchs CS, Baselga J, Tabernero J, Gabriel S, Lander ES, Getz G, Meyerson
M. Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1ATCF7L2 fusion. Nat Genet. 2011 Sep 4 [Epub ahead of print].
* Co-corresponding authors.
17
Review Articles and Editorials
1. Signoretti S, Loda M. Estrogen receptor beta in prostate cancer: brake pedal or accelerator?
Am J Pathol 2001;159:13-6.
2. Signoretti S and Loda M. Defining stem cells in the prostate epithelium. Cell Cycle. 2006;
5:138-41.
3. Cho D, Signoretti S, Regan M, Mier JW, Atkins MB. The role of mammalian target of
rapamycin inhibitors in the treatment of advanced renal cancer. Clin Cancer Res. 2007;13(2
Pt 2):758s-763s.
4. Signoretti S and Loda M. Prostate stem cells: from development to cancer. Semin Cancer
Biol. 2007; 17(3):219-24.
5. Grisanzio C and Signoretti S. p63 in prostate biology and pathology. J Cell Biochem. 2008;
103(5):1354-68.
6. Signoretti S, Regan M, Atkins MB. Carbonic Anhydrase IX (CAIX) as a predictive
biomarker of response to kidney cancer therapy. BJU Int. 2008; 101 Suppl 4:31-5.
7. Signoretti S, Bratslavsky G, Waldman FM, Reuter VE, Haaga J, Merino M, Thomas GV,
Pins MR, Libermann T, Gillespie J, Tomaszewski JE, Compton CC, Hruszkewycz A,
Linehan WM, Atkins MB. Tissue-Based Research In Kidney Cancer: Current Challenges
And Future Directions. Clin Cancer Res. 2008;14(12):3699-705.
8. Signoretti S. Tissue-Based Research in the Era of ‘Personalized Medicine’: Biomarkers,
Microarrays, and Beyond. Kidney Cancer Journal. 2008;235-9.
9. Di Napoli A and Signoretti S. Tissue Biomarkers in Renal Cell Carcinoma: Issues and
Solutions. Cancer. 2009;115(10 Suppl):2290-7.
10. Atkins MB, Choueiri TK, Cho D, Regan M, Signoretti S. Treatment Selection for Patients
With Metastatic Renal Cell Carcinoma. Cancer. 2009;115(10 Suppl):2327-33.
11. Atkins MB, Bukowski RM, Escudier BJ, Figlin RA, Hudes GH, Kaelin WG Jr, Linehan
WM, McDermott DF, Mier JW, Pedrosa I, Rini BI, Signoretti S, Sosman JA, The BT, Wood
CG, Zurita, AJ and King L. Innovations and Challenges in Renal Cancer: Summary
Statement From the Third Cambridge Conference. Cancer. 2009;115(10 Suppl):2247-51.
Chapters in Books
1. Kamino H, Signoretti S, Weedon D. Site specific nevi. In “WHO classification of tumors:
Pathology and Genetics of Skin Tumors”. Edited by LeBoit PE, Burg G, Weedon D, Sarasin
A.
2. Grisanzio C and Signoretti S. Adult Prostate Epithelium Renewal, Stem Cells and Cancer. In
“Stem Cells and Cancer”. Edited by Rebecca G. Bagley and Beverly A. Teicher. 2009.
3. Bahamon B and Signoretti S. Tissue Biomarkers in Renal Cell Carcinoma: Intermediate
Endpoints in the Selection of Targeted Agents for RCC. In “Renal Cell Carcinoma:
18
Biology, Prognostic Factors and Therapeutic Targets”. Edited by Kimryn Rathmell, Brian
Rini and Robert A. Figlin. In Press.
Thesis
1. M.D. Thesis: Signoretti S. Cyclosporin nephrotoxicity in kidney transplantation. University
of Rome, 1988.
2. Pathology Residency Thesis: Signoretti S. Congenital cystic adenomatoid, malformation of
the lung. University of Rome, 1993.
Patents
1. 1999. Loda M, Macri’ E, Signoretti S. “Cdx-2 as a unique marker of colon carcinoma”
2.
1999. Harvard Medical School, Harvard Case #1674. McKeon F, Yang A, Loda M,
Signoretti S, Crum C. “p63 expression pattern in the classification of malignancies of the
prostate, cervix and breast”
Abstracts (Unpublished work)
1. Grisanzio C, Sabbisetti V, Browne D, Signoretti S. p63 in Development and Maintenance of
the Prostate Epithelium. Department of Defense Prostate Cancer Research Program Meeting.
Innovative minds in Prostate Cancer Today (IMPaCT). Atlanta, Georgia 2007.
2. Han WK, Hsiao L, Signoretti S, Bonventre JV, Steele G. Kidney Injury Molecule- (KIM-1)
and carbonic Anhydrase IX (CAIX) as Urinary Biomarkers for Renal Cell Carcinoma. J Am
Soc Nephrol. 2007; 18:222A.
3. Di Napoli A, Grisanzio C, Ghebremichael M, Seeley A, Amato AM, Atkins MB, Signoretti S.
CAIX Expression Correlates with VHL Mutational Status in Sporadic Clear Cell Carcinoma
of the Kidney. Annual Meeting United States and Canadian Division of the International
Academy of Pathology, Denver, Colorado, 2008.
19