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Tumor Suppressor Gene




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. However, there are cases where mutations in only one allele will cause an effect. A notable example is the gene that codes for P53 .

Tumor suppressor genes, or more precisely, the Protein s for which they Code , either have a dampening or repressive effect on the regulation of the Cell Cycle or promote Apoptosis , and sometimes do both. The functions of tumor suppressor proteins fall into several categories {Link without Title} including:
# 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 Cell Division .
# Coupling the cell cycle to DNA Damage . As long as there is damaged DNA in the cell, it should not divide. If the damage can be repaired, the cell cycle can continue.
# If the damage can ''not'' be repaired, the cell should initiate Apoptosis , or programmed cell death, to remove the threat it poses for the greater good of the organism.
# Some proteins involved in Cell Adhesion prevent tumor cells from dispersing, block loss of Contact Inhibition , and inhibit Metastasis {Link without Title}

The first tumor suppressor protein discovered was the '' PRb Protein '' in Human Retinoblastoma ; however, recent evidence has also implicated pRb as a tumor survival factor. Another important tumor suppressor is the P53 Gene .


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