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Cancer Genetics and Epigenetics 2013, Vol.1, No.1, 1-2 http://cge.biopublisher.ca Lanuching Words Open Access Cancer research advantaged in genetics and epigenetics progress Yan Zhang College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150081, China Corresponding author email: [email protected] Cancer Genetics and Epigenetics, 2013, Vol.1, No.1 doi: 10.5376/cge.2013.01.0001 Received: 01 Nov., 2013 Accepted: 01 Nov., 2013 Published: 01 Nov., 2013 Copyright © 2013 Zhang, This is an open access article published under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Preferred citation for this article: Zhang, 2013, Cancer research advantaged in genetics and epigenetics progress, Cancer Genetics and Epigenetics, Vol.1, No.1 1-2 Abstract Cancers now have been regarded as complex diseases caused by the abnormity of genetics or epigenetics and the most affective disease for the life of human around the world. In the last decade, it is an opportunity to identify more and more novel biomarkers in genome level along with the outbreak of biological data. For the current biomedical field, biomarker identification is also an important step for translational medicine. Meanwhile, earlier studies have identified many cancer biomarkers with genetic alterations. Genomics and epigenomics are playing more and more important roles in the treatment of cancers. Keywords Cancer; Biomarker; Genetics; Gpigenetics Earlier studies have identified many cancer biomarkers with genetic alterations. For example, BRAF mutations happened in ovarian cancer and were identified as a candidate biomarker for the promising prognosis of ovarian cancer (Estep et al., 2007). However, epigenetic alteration is also one of the many important factors in cancers. Through the recent literatures, many epigenetically altered cancer biomarkers have been recognized. Recently, CpG island methylation alteration has been associated with cancer development, which is a common biomarker. For example, TFPI2 or GATA4 methylation has been found to be good predictors of colon cancer by examining patient excrement (Feinberg et al., 2006). In addition, RASSF1A has been predicted to be an indicator of poor prognosis in various cancers (Jiang et al., 2012; Wang et al., 2008). Partner of SLD5 1 (PSF1), a conserved replication factor in evolution, was demonstrated to correlate with diagnosis of cancers and was expressed differentially in prostate cancer. Therefore it was regarded as a biomarker to diagnose the patients with poor prognosis (Nagahama et al., 2010). The hypermethylation of PITX2 increased the risk of prostate cancer and could be a useful biomarker for poor survival (Vinarskaja et al., 2013). The up-regulation of methylation in Polo-like kinase (PLK) increased the probability of mutation and it was associated with oncogenes. The hypermethylation of P16 gene could increase the risk With the development of oncology, more accurate biomarkers are still needed for the early detection of diseases. The biomarkers not only contribute to the early prevention, detection and prognosis of diseases, but also engage in the personalized medicine which could provide more effective treatment programs based on the characteristics of patients. In the last decade, it is an opportunity to identify more and more novel biomarkers in genome level along with the outbreak of biological data. For the current biomedical field, biomarker identification is also an important step for translational medicine. Cancers have been regarded as complex diseases caused by the abnormity of genetics or epigenetics and the most affective disease for the life of human around the world. In the past ten years, we have focused on the researches in molecular level based on the development of the researches of cause and pathogenic mechanism for cancers and epigenetics is one of the most important research fields in our researches. Many biologists have realized that the pathogenesis of cancer is not only caused by the abnormity of genetic elements but also the abnormity of epigenetic modifications. Therefore, genomics and epigenomics are both the important research hotspots of cancer in post-genome time and the crosstalk between genomics and epigenomics could offer novel possibilities for cancer therapy. 1 Cancer Genetics and Epigenetics 2013, Vol.1, No.1, 1-2 http://ijms.biopublisher.ca of esophageal cancer and also be a biomarker for the identification of esophageal cancer (Hardie et al., 2005). Therefore, molecular biomarkers may be useful for predicting the disease states of given patients. Barrett's esophagus and esophageal adenocarcinoma: association with genetic and epigenetic alterations, Cancer Lett, 217: 221-230 http://dx.doi.org/10.1016/j.canlet.2004.06.025 Jiang Y., Cui L., Chen W.D., Shen S.H., and Ding L.D., 2012, The prognostic role of RASSF1A promoter methylation in breast cancer: a meta-analysis of published data, PLoS One, 7: e36780 http://dx.doi.org/10.1371/journal.pone.0036780 Nagahama Y., Ueno M., Miyamoto S., Morii E., Minami T., Mochizuki N., Saya H., and Takakura N., 2010, PSF1, a DNA replication factor expressed widely in stem and progenitor cells, drives tumorigenic and metastatic properties, Cancer Res, 70: 1215-1224 http://dx.doi.org/10.1158/0008-5472.CAN-09-3662 Vinarskaja A., Schulz W.A., Ingenwerth M., Hader C., and Arsov C., 2013, Association of PITX2 mRNA down-regulation in prostate cancer with promoter hypermethylation and poor prognosis, Urol Oncol, 31: 622-627 http://dx.doi.org/10.1016/j.urolonc.2011.04.010 Wang S.H., Liu N.H., Wang J., Bai H., and Mao L., 2008, Critical role of deltaDNMT3B4/2 in regulating RASSF1A promoter-specific DNA methylation in non-small cell lung cancer, Chin Med J (Engl), 121: 1712-1721 In conclusion, genomics and epigenomics have important roles in the treatment of cancers. From now on, we will pay more attention to the field of cancer genomics and epigenomics. The amazing progress in this field will hopefully uncover the mechanism of cancers eventually. In addition, the creation of new methods for the prevention and treatment of cancers will aid discovering the potential cancer targets. References Estep A.L., Palmer C., Mccormick F., and Rauen K.A., 2007, Mutation analysis of BRAF, MEK1 and MEK2 in 15 ovarian cancer cell lines: implications for therapy, PLoS One, 2: e1279 http://dx.doi.org/10.1371/journal.pone.0001279 Feinberg A.P., Ohlsson R., and Henikoff S., 2006, The epigenetic progenitor origin of human cancer, Nat Rev Genet, 7: 21-33 http://dx.doi.org/10.1038/nrg1748 Hardie L.J., Darnton S.J., Wallis Y.L., Chauhan A., Hainaut P., Wild C.P., and Casson A.G., 2005, p16 expression in 2