دورية
Serrated polyps and colorectal cancer risk
| العنوان: | Serrated polyps and colorectal cancer risk |
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| المؤلفون: | Mäkinen, Markus J |
| المصدر: | Colorectal Cancer; January 2014, Vol. 3 Issue: 1 p77-91, 15p |
| مستخلص: | SUMMARY Colorectal cancer is among the three most common cancers in the World with a global incidence exceeding 1.2 million new cases and 600,000 deaths per year; yet most cases could be prevented by endoscopic removal of precursor lesions. Efficient screening and follow-up are the best options to reduce the cancer burden caused by colorectal cancer (CRC). Therefore, it is essential to know which colorectal polyps have the potential to progress into cancer. During the last decade, serrated polyps have emerged as the second most important group of CRC precursor lesions, in addition to conventional adenomatous polyps. It has been estimated that up to 30–35% of CRCs have their origin in serrated polyps. Carcinogenesis via serrated polyps, known as the serrated pathway, requires activation of the MAPK pathway by mutations of BRAFand KRAS, and low- or high-level methylation of CpG islands of DNA (CpG island methylator phenotype), and subsequent high-level DNA microsatellite instability in a third of cases. The mechanisms involved in carcinogenesis via the serrated pathway profoundly differ from those of conventional adenoma–carcinoma pathway, and the biology and behavior of serrated polyps also differ from that of adenomatous polyps, which are characterized by chromosomal instability and loss of tumor suppressor genes. |
| قاعدة البيانات: | Supplemental Index |
| تدمد: | 1758194X 17581958 |
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| DOI: | 10.2217/crc.13.84 |