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结肠癌患者形态学正常结肠中的DNA非整倍体

DNA aneuploidy in morphologically normal colons from patients with colon cancer.

作者信息

Fleischhacker M, Lee S, Spira S, Takeuchi S, Koeffler H P

机构信息

Department of Hematology/Oncology, Cedars-Sinai Medical Center, Los Angeles, California.

出版信息

Mod Pathol. 1995 May;8(4):360-5.

PMID:7567931
Abstract

DNA aneuploidy is common in colon carcinoma, colonic polyps, and ulcerative colitis. We found an interesting subset of patients with colon cancer. These individuals (14 of 230 cases, 6%) had hypodiploid aneuploidy in their morphologically normal-appearing colonic tissue. The aneuploid fractions were small, making up between 10 to 15% of the total events, and the ploidy pattern was not related to the ploidy pattern of the tumor. The clinical findings of the 14 patients were compared with those of patients who had diploid normal colons by age, location of the tumor, Dukes stage, and percent aneuploidy in the main tumor; the two groups were comparable. Both the normal colon and carcinomas of the 14 cases were studied by a newly developed "enriched" polymerase chain reaction for K-ras mutations. No K-ras mutations were found in the normal tissues, but mutations were found in the tumors of four cases. Cells from some colon cancers have a high degree of genetic instability, as shown by numerous mutations throughout the genome. Analysis of eight matched colon cancers and aneuploid, morphologically normal-appearing colons for genetic alterations, as measured by shifts in the electrophoretic mobility of microsatellite repeat fragments, showed that only one of eight colon cancer samples had microsatellite instability, which is the expected frequency. Taken together, the data suggest that individuals with colon cancer may have morphologically normal colonic tissue, which is genetically abnormal, and this abnormality may precede the development of mutations in K-ras.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

DNA非整倍体在结肠癌、结肠息肉和溃疡性结肠炎中很常见。我们发现了一组有趣的结肠癌患者。这些个体(230例中有14例,占6%)在其形态学上看似正常的结肠组织中存在亚二倍体非整倍体。非整倍体部分较小,占总事件的10%至15%,并且倍体模式与肿瘤的倍体模式无关。将这14例患者的临床发现与年龄、肿瘤位置、杜克分期以及主要肿瘤中的非整倍体百分比方面结肠二倍体正常的患者进行比较;两组具有可比性。对这14例患者的正常结肠和癌组织均采用新开发的用于K-ras突变检测的“富集”聚合酶链反应进行研究。在正常组织中未发现K-ras突变,但在4例患者的肿瘤中发现了突变。一些结肠癌的细胞具有高度的基因不稳定性,这可通过全基因组中的大量突变得以体现。通过微卫星重复片段电泳迁移率的变化来测量,对8对匹配的结肠癌和非整倍体、形态学上看似正常的结肠进行基因改变分析,结果显示8个结肠癌样本中只有1个具有微卫星不稳定性,这是预期的频率。综上所述,数据表明患有结肠癌的个体可能有形态学上正常但基因异常的结肠组织,并且这种异常可能先于K-ras突变的发生。(摘要截短至250字)

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