Wang Yue, Liu Vincent W S, Ngan Hextan Y S, Nagley Phillip
Department of Obstetrics & Gynecology, University of Hong Kong, Hong Kong SAR, China.
Ann N Y Acad Sci. 2005 May;1042:123-9. doi: 10.1196/annals.1338.012.
We analyzed the occurrence of mitochondrial microsatellite instability (mtMSI) in 262 pairs of female cancer tissues with the matched normal controls. mtMSI was detected in only 4 of 12 microsatellites found in the mitochondrial genome (3 in the D-loop and 1 in the 12S rRNA gene). Interestingly, 95.6% (87/91) of mtMSI was detected in the D-loop, namely, at nucleotide positions 303-315, 514-523, and 16184-16193. This demonstrates that the D-loop is a hotspot for mtMSI. Different incidences of mtMSI at these three microsatellites were found in the four cancer types (including cervical, endometrial, ovarian, and breast). Together with those mtMSI reported in other studies, the differential occurrence of mtMSI at each of the markers in the D-loop region was observed, indicating that the extent of mtMSI varies from one cancer to another. Although the mechanisms of generation and functional impact of mtMSI are still not clear, the high incidence of mtMSI in the D-loop and its broad distribution in human cancers render it a potential marker for cancer detection.
我们分析了262对女性癌组织及其配对的正常对照中线粒体微卫星不稳定性(mtMSI)的发生情况。在线粒体基因组中发现的12个微卫星中,仅在4个微卫星中检测到mtMSI(3个在D环,1个在12S rRNA基因)。有趣的是,95.6%(87/91)的mtMSI在D环中被检测到,即在核苷酸位置303 - 315、514 - 523和16184 - 16193处。这表明D环是mtMSI的一个热点区域。在四种癌症类型(包括宫颈癌、子宫内膜癌、卵巢癌和乳腺癌)中,这三个微卫星处的mtMSI发生率不同。结合其他研究报道的mtMSI情况,观察到D环区域各标记处mtMSI的发生存在差异,表明mtMSI的程度在不同癌症之间有所不同。尽管mtMSI的产生机制和功能影响仍不清楚,但D环中mtMSI的高发生率及其在人类癌症中的广泛分布使其成为癌症检测的一个潜在标志物。