Akrami Seyed Mohammad
Department of Medical Genetics, Endocrinology and Metabolism Research Center (EMRC), Tehran University of Medical Sciences, Tehran, Iran.
Arch Iran Med. 2006 Oct;9(4):381-9.
Colorectal cancer is a major cause of morbidity and mortality. About 15 - 20% of all colorectal cancers are familial. Hereditary nonpolyposis colorectal cancer is an inherited cancer predisposition syndrome. It is caused by mutations in mismatch repair genes, predominantly MSH2 and MLH1. Although hereditary nonpolyposis colorectal cancer accounts for a minority of colorectal cancers, the mutations identified in these cases are important in our understanding of colorectal cancer pathogenesis. An increasing number of deletions in different exons of MSH2 and MLH1 genes is reported to result in hereditary nonpolyposis colorectal cancer. This paper reviews the genetics behind these genes and molecular study of the hereditary nonpolyposis colorectal cancer. This may help the medical professionals especially internists, gastroenterologists, and oncologists to update their knowledge in this field.
结直肠癌是发病和死亡的主要原因。所有结直肠癌中约15%-20%为家族性。遗传性非息肉病性结直肠癌是一种遗传性癌症易感性综合征。它由错配修复基因的突变引起,主要是MSH2和MLH1。虽然遗传性非息肉病性结直肠癌占结直肠癌的少数,但在这些病例中鉴定出的突变对于我们理解结直肠癌的发病机制很重要。据报道,MSH2和MLH1基因不同外显子中越来越多的缺失会导致遗传性非息肉病性结直肠癌。本文综述了这些基因背后的遗传学以及遗传性非息肉病性结直肠癌的分子研究。这可能有助于医学专业人员,尤其是内科医生、胃肠病学家和肿瘤学家更新他们在该领域的知识。