Brentnall T A, Crispin D A, Bronner M P, Cherian S P, Hueffed M, Rabinovitch P S, Rubin C E, Haggitt R C, Boland C R
Department of Medicine, University of Washington, Seattle 98195, USA.
Cancer Res. 1996 Mar 15;56(6):1237-40.
Microsatellite instability (MIN) has been detected in many cancer types; however, recently we also observed it in the nonneoplastic but inflammatory setting of pancreatitis. Consequently, we sought to examine whether MIN was present in another inflammatory condition, ulcerative colitis (UC). MIN was found in 50% of UC patients whose colonic mucosa was negative for dysplasia, 46% of those with high-grade dysplasia, and 40% of those with cancer but in none of the ischemic or infectious colitis controls (P<0.03). Thus, UC patients may have MIN within mucosa that has no histological evidence of neoplastic change. MIN in this setting may reflect the inability of DNA repair mechanisms to compensate for the stress of chronic inflammation, and may be one mechanism for the heightened neoplastic risk in UC.
微卫星不稳定性(MIN)已在多种癌症类型中被检测到;然而,最近我们也在胰腺炎的非肿瘤性但炎症性环境中观察到了它。因此,我们试图研究MIN是否存在于另一种炎症性疾病——溃疡性结肠炎(UC)中。在结肠黏膜发育异常阴性的UC患者中,50%检测到MIN;在高级别发育异常患者中,46%检测到MIN;在癌症患者中,40%检测到MIN,但在缺血性或感染性结肠炎对照组中均未检测到(P<0.03)。因此,UC患者在没有肿瘤性改变组织学证据的黏膜内可能存在MIN。这种情况下的MIN可能反映了DNA修复机制无法补偿慢性炎症的压力,并且可能是UC中肿瘤风险增加的一种机制。