Tumor suppressor gene
A tumor suppressor gene, or antioncogene is a
genethat protects a cell from one step on the path to cancer. When this gene is mutated to cause a loss or reduction in its function, the cell can progress to cancer, usually in combination with other genetic changes.
Unlike oncogenes, tumor suppressor genes generally follow the '
two-hit hypothesis', which implies that both alleles that code for a particular gene must be affected before an effect is manifested. This is due to the fact that if only one allele for the gene is damaged, the second can still produce the correct protein. In other words, mutant tumor suppressors alleles are usually recessive whereas mutant oncogene alleles are typically dominant. The two hit hypothesis was first proposed by A.G. Knudson for cases of retinoblastoma. [cite journal |author=Knudson AG |title=Mutation and cancer: statistical study of retinoblastoma |journal=Proc Natl Acad of Sci |volume=68 |issue=4 |pages=820–3 |year=1971 |pmid=5279523 |doi=10.1073/pnas.68.4.820] Knudson observed that the age of onset of retinoblastoma followed 2nd-order kinetics, implying that two independent genetic events were necessary. He recognized that this was consistent with a recessive mutation involving a single gene, but requiring biallelic mutation. Oncogenemutations, in contrast, generally involve a single allele because they are gain of function mutations. There are notable exceptions to the 'two hit' rule for tumors suppressors, such as certain mutations in the p53 gene product. p53 mutations can function as a 'dominant negative', meaning that a mutated p53 protein can prevent the function of normal protein from the un-mutated allele. [cite journal |author=Baker SJ, Markowitz S, Fearon ER, Willson JK, Vogelstein B. |title=Suppression of human colorectal carcinoma cell growth by wild-type p53. |journal=Science |volume=249 |issue=4971 |pages=912–5 |year=1990 |pmid= 2144057 |doi=10.1126/science.2144057] Other tumor suppressor genes which are exceptions to the 'two-hit' rule are those which exhibit haploinsufficiency. An example of this is the p27Kip1 cell cycle inhibitor, in which mutation of a single allele causes increased carcinogen susceptibility. [cite journal |author=Fero ML, Randel E, Gurley KE, Roberts JM, Kemp CJ |title=The murine gene p27Kip1 is haplo-insufficient for tumour suppression |journal=Nature |volume=396 |issue=6707 |pages=177–80 |year=1998 |pmid=9823898 |doi=10.1038/24179]
Tumor suppressor genes, or more precisely, the
proteins for which they code, either have a dampening or repressive effect on the regulation of the cell cycleor promote apoptosis, and sometimes do both. The functions of tumor suppressor proteins fall into several categories including the following: [cite journal |author=Sherr C |title=Principles of tumor suppression |journal=Cell |volume=116 |issue=2 |pages=235–46 |year=2004 |pmid=14744434 | doi = 10.1016/S0092-8674(03)01075-4 ]
# Repression of genes that are essential for the "continuing" of the cell cycle. If these genes are not expressed, the cell cycle will not continue, effectively inhibiting
# Coupling the cell cycle to
DNA damage. As long as there is damaged DNAin the cell, it should not divide. If the damage can be repaired, the cell cycle can continue.
# If the damage "cannot" be repaired, the cell should initiate
apoptosis(programmed cell death) to remove the threat it poses for the greater good of the organism.
# Some proteins involved in
cell adhesionprevent tumor cells from dispersing, block loss of contact inhibition, and inhibit metastasis. These proteins are known as metastasis suppressors. [Yoshida, BA, Sokoloff, MM, Welch, DR, Rinker-Schaeffer CW. 2000. [http://jnci.oxfordjournals.org/cgi/content/full/92/21/1717 Metastasis-suppressor genes: a review and perspective on an emerging field.] Journal of the National Cancer Institute 92: 1717-1730.] [cite journal |author=Hirohashi S, Kanai Y |title=Cell adhesion system and human cancer morphogenesis |journal=Cancer Sci |volume=94 |issue=7 |pages=575–81 |year=2003 |pmid=12841864 | doi = 10.1111/j.1349-7006.2003.tb01485.x ]
The first tumor suppressor protein discovered was the
Retinoblastoma protein(pRb) in human retinoblastoma; however, recent evidence has also implicated pRb as a tumor survival factor.
Another important tumor suppressor is the
p53tumor suppressor protein encoded by the TP53gene. Homozygous loss of p53 is found in 70% of colon cancers, 30-50% of breast cancers and 50% of lung cancers. Mutated p53 is also involved in the pathophysiology of leukemias, lymphomas, sarcomas and neurogenic tumors. Abnormalities of the p53 gene can be inherited in Li-Fraumeni syndrome(LFS), which increases the risk of developing various types of cancers. PTENacts by opposing the action of PI3K, which is essential for anti-apoptotic, pro-tumorogenic Aktactivation.
Other examples of tumour suppressors include APC and
*Adenomatosis polyposis coli
Von Hippel Lindau Binding protein 1
* [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=books&doptcmdl=GenBookHL&term=Tumor+suppressor+gene+AND+cmed6%5Bbook%5D+AND+354309%5Buid%5D&rid=cmed6.section.22504#22514 Cancer Medicine] , online textbook.
* [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=books&doptcmdl=GenBookHL&term=Tumor+suppressor+gene+AND+hmg%5Bbook%5D+AND+227209%5Buid%5D&rid=hmg.section.2377 Human Molecular Genetics] , online textbook.
* [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=books&doptcmdl=GenBookHL&term=Tumor+suppressor+gene+AND+iga%5Bbook%5D+AND+101379%5Buid%5D&rid=iga.section.3619#3636 Introduction to Genetic Analysis] , online textbook.
* [http://researchnews.osu.edu/archive/lungcagn.htm TCF21 gene discovery at Ohio State University]
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Look at other dictionaries:
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