Hutchison Jennifer, Cohen Zoe, Onyeagucha Benjamin C, Funk Janet, Nelson Mark A
Physiological Sciences Interdisciplinary Program, University of Arizona, Tucson, Arizona, USA.
Cancer Genet. 2013 Sep-Oct;206(9-10):309-16. doi: 10.1016/j.cancergen.2013.06.005. Epub 2013 Sep 14.
MicroRNAs have emerged as important post-translational regulators of gene expression and are involved in several physiological and pathological states including the pathogenesis of human colon cancers. In regards to tumor development, microRNAs can act as oncogenes or tumor suppressors. Two hereditary predispositions (i.e., Lynch syndrome and familial adenomatous polyposis) contribute to the development of colon cancer. In addition, individuals who suffer from inflammatory bowel diseases such as Crohn's disease or ulcerative colitis have a higher risk of developing colon cancer. Here, we discuss the occurrence of the deregulated expression of microRNAs in colon cancer that arise as a result of hereditary predisposition and inflammatory bowel disease.
微小RNA已成为基因表达重要的翻译后调节因子,并参与多种生理和病理状态,包括人类结肠癌的发病机制。在肿瘤发展方面,微小RNA可作为癌基因或肿瘤抑制因子。两种遗传易感性(即林奇综合征和家族性腺瘤性息肉病)促成结肠癌的发生。此外,患有诸如克罗恩病或溃疡性结肠炎等炎症性肠病的个体患结肠癌的风险更高。在此,我们讨论因遗传易感性和炎症性肠病导致的结肠癌中微小RNA表达失调的情况。