Epigenetic Markers of Early Tumor Development

Cancer patients’ outcome and survival depends on the early diagnosis of malignant lesions. Several investigation methods used for the prevention and early detection strategies have specific limitations. More recently, epigenetic changes have been considered one of the most promising tools for the early diagnosis of cancer. Some of these epigenetic alterations including promoter hypermethylation of genes likeP16INK4a,BRCA1,BRCA2,ERαandRARβ2,APC, andRASSF1Ahave been associated with early stages of mammary gland tumorigenesis and have been suggested to be included in the models that evaluate individual breast cancer risk. In lung cancer,P16INK4aandMGMTgene hypermethylation was observed in sputum years before clinical manifestation of the squamous cell carcinoma among smokers. Loss ofGSTP1function by DNA hypermethylation together with changes in the methylation levels of repetitive elements like LINE-1 and Sat2 was reported in prostatic preneoplastic lesions. Also, DNA hypermethylation forhMLH1andMGMTDNA repair genes was reported in precursor lesions to colorectal cancer. These epigenetic alterations may be influenced by factors such as xenoestrogens, folate, and multivitamins. Detection of these changes may help determining cancer susceptibility and early diagnosis.

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