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Cancer &Oncogenes Objectives • Define the terms oncogene, proto-oncogenes and growth factors giving examples. • Describe the mechanisms of activations of protooncogenes and their roles in carcinogenesis. Reference: Textbook of Medical Biochemistry, 7th edition. Section 7, chapter46 (Biochemistry of cancer). Pages:737-744. Define proto-oncogenes oncogene,and growth factors * A proto-oncogene is a normal gene that can become an oncogene due to mutations or increased expression. The proto-onncogenes converted to ocogenes and develop cancer. * A mutant proto-oncogene whose protien product is involved in the transformation of normal cell to cancer cell. * An oncogene can be defined as an altered gene whose product acts in a dominant manner to accelerate cell growth or cell division. Carcinogenesis Oncogenes and Tumor Suppressor Genes In normal cell, two categories of cell regulatory genes: • Proto-oncogenes (cellular oncogene, c-onc) • Tumor suppressor gene Proto-oncogenes oncogenes increase growth rate cancer Tumor suppressor genes inactivated cancer Proto-oncogenes code for: • Growth factors • Receptors • Signal transduction factors Differences between oncogenes & Tumor suppressor genes Oncogenes Mutation in one of the two alleles is sufficient Tumor suppressor genes Both alleles must be affected Gain of function of a protein that Loss of function of protein signals cell division Mutation arises in somatic cells, not inherited Mutation present in germ cell (inherited ) or in somatic cell Some tissue preference Often strong tissue preference NORMAL CELL Growth factor Growth factor receptor cytoplasm Signal transduction nucleus Activation of transcription Relationship between gene products of proto oncogene Growth factors eg IGF Growth factor receptors Eg erb-2, ret Signal transducing factors Eg cytoplasmic kinases cell cycle proteins eg cyclin D DNA binding proteins concerned with transcription Tumor suppressor gene (antioncogenes): • It is a gene that protects a cell from cancer. – Tumor suppressor genes code for factors that downregulate the cell cycle • P53 • Rb p53: it codes for a regulatory protein that turns off cell division when the cell is stressed or damaged. If mutated, runaway cell division More than half of cancers has a mutated or missing p53 gene NEOPLASTIC CELLS Increased In growth factor Increased In growth factor receptors Increased in signal transduction Increase in activation of transcription How does proto-oncogenes get activated into oncogenes? – Enhancer insertion – Promoter insertion – translocation – gene amplification – point mutation • Point mutations, insertions or deletions that give rise to an overactive gene product or lead to an increase in transcription. • Gene amplification leading to additional copies of proto-oncogene • Chromosomal tranlocation that causes a protooncogene to move to a different chromosomal site associated with increased expression or to fuse with another gene to produce a protien that has oncogenic aactivity. Viral oncogenes RNA Retrovirus: Produces DNA provirus which contain viral oncogene (v- onc) DNA virus: DNA viruses form stable association with host cell genome. • A Reverse transcriptase ( RT) is An enzyme used to generate complementary DNA (c DNA) from an RNA template, a process termed reverse transcription. It is mainly associated with retrovirusses. Products of viral oncogenes Viral oncogenes Products erb-B Epidermal growth factor (EGF) ras GTP binding protein myc Nuclear protein modify cell growth src Protein tyrosine kinase sis Truncated platelet derived growth factor (PDGF) Growth factors Growth factor is a naturally occurring substance capable of stimulating cellular growth and differentiation, it is usually protein in nature. Types of growth factors: Mechanism of action of growth factors: Endocrine, Paracrine and Autocrine. Action of growth factors: Types of cancer genes Type of gene Normal function Mutated function Types of proteins Oncogene Promotes division Promotes division abnormal time or cell type Growth factors Tumor suppressor gene Suppresses cell division Fails to suppress division Checkpoint molecules DNA repair gene mutation Repair DNA mutations Fail to repair DNA mutations Enzymes for mismatch or excision repair