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息肉病和非息肉病患者结直肠腺瘤的染色体数目分布及细胞DNA含量

Chromosome number distribution and cellular DNA content in colorectal adenomas from polyposis and nonpolyposis patients.

作者信息

Petersen S E, Madsen A L, Bak M

机构信息

Department of Experimental Clinical Oncology, Danish Cancer Society, Aarhus.

出版信息

Cancer Genet Cytogenet. 1991 Jun;53(2):219-28. doi: 10.1016/0165-4608(91)90098-f.

Abstract

Ploidy analyses of colorectal adenomas were performed by combined flow cytometric DNA analysis of unfixed isolated nuclei and direct chromosome preparation after Colcemid incubation for 9-20 hours. Ten of 18 adenomas from nonpolyposis patients and 4 of 13 adenomas from patients with familial adenomatous polyposis yielded a mean of 25 countable metaphases (range 7-44) per tumor. Of 343 metaphases, only 38% had 46 chromosomes, and 62% were nondiploid. All but one adenoma had diploid or peridiploid modes in the range of 46-50 chromosomes. One adenoma was hyperploid, with a mode of 74 chromosomes and a correspondingly increased nuclear DNA content. In another two adenomas, the DNA analyses showed small hyperploid populations constituting 6% and 2% of the cells. The most striking difference between the DNA analyses and chromosome number distributions was that 13% of all metaphases were hyperploid with chromosome numbers outside the perimodal range but, except in one adenoma, without indication in the DNA histogram of corresponding hyperploid cell populations. We propose that these aberrant metaphases indicate an early acquired genetic instability of the neoplastic epithelium, which may be instrumental in generation of hyperploid, invasive clones, which constitute most colorectal carcinomas.

摘要

通过对未固定的分离细胞核进行流式细胞术DNA分析,并在秋水仙胺孵育9 - 20小时后直接制备染色体,对结直肠腺瘤进行倍性分析。18例非息肉病患者的腺瘤中有10例,13例家族性腺瘤性息肉病患者的腺瘤中有4例,每个肿瘤平均产生25个可计数的中期分裂相(范围为7 - 44)。在343个中期分裂相中,只有38%有46条染色体,62%为非二倍体。除1例腺瘤外,所有腺瘤的二倍体或亚二倍体模式的染色体数在46 - 50条范围内。1例腺瘤为超倍体,模式染色体数为74条,核DNA含量相应增加。在另外2例腺瘤中,DNA分析显示超倍体细胞群体分别占细胞总数的6%和2%。DNA分析和染色体数分布之间最显著的差异是,所有中期分裂相中有13%为超倍体,其染色体数超出了模式周边范围,但除1例腺瘤外,DNA直方图中没有相应超倍体细胞群体的迹象。我们认为这些异常的中期分裂相表明肿瘤上皮细胞早期获得性遗传不稳定,这可能有助于产生构成大多数结直肠癌的超倍体、侵袭性克隆。

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