A report on Familial adenomatous polyposis, Colorectal cancer and Carcinogenesis
While these polyps start out benign, malignant transformation into colon cancer occurs when they are left untreated.
- Familial adenomatous polyposisSome of the inherited genetic disorders that can cause colorectal cancer include familial adenomatous polyposis and hereditary non-polyposis colon cancer; however, these represent less than 5% of cases.
- Colorectal cancer(APC regulates β-catenin, a protein that plays a crucial role in cell communication, signalling, growth, and controlled destruction, but which left uncontrolled also gives rise to numerous cancers ).
- Familial adenomatous polyposisAs summarized in the articles Carcinogenesis and Neoplasm, for sporadic cancers in general, a deficiency in DNA repair is occasionally due to a mutation in a DNA repair gene, but is much more frequently due to epigenetic alterations that reduce or silence expression of DNA repair genes.
- Colorectal cancerOther inherited tumor suppressor gene syndromes include Rb mutations, linked to retinoblastoma, and APC gene mutations, linked to adenopolyposis colon cancer.
- CarcinogenesisAdenopolyposis colon cancer is associated with thousands of polyps in colon while young, leading to colon cancer at a relatively early age.
- Carcinogenesis1 related topic with Alpha
Cancer
0 linksGroup of diseases involving abnormal cell growth with the potential to invade or spread to other parts of the body.
Group of diseases involving abnormal cell growth with the potential to invade or spread to other parts of the body.
Early detection through screening is useful for cervical and colorectal cancer.
Several studies have indicated that the enzyme sirtuin 6 is selectively inactivated during oncogenesis in a variety of tumor types by inducing glycolysis.
COX-2 inhibitors may decrease the rate of polyp formation in people with familial adenomatous polyposis; however, it is associated with the same adverse effects as NSAIDs.