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9p21的等位基因缺失和CDKN2/p16基因的突变在巴雷特食管的肿瘤进展过程中作为早期病变出现。

Allelic loss of 9p21 and mutation of the CDKN2/p16 gene develop as early lesions during neoplastic progression in Barrett's esophagus.

作者信息

Barrett M T, Sanchez C A, Galipeau P C, Neshat K, Emond M, Reid B J

机构信息

Public Health Sciences, Fred Hutchinson Cancer Research Center, University of Washington, Seattle 98195, USA.

出版信息

Oncogene. 1996 Nov 7;13(9):1867-73.

PMID:8934532
Abstract

High frequency allelic loss of chromosome 9p21 has been reported in a number of human cancers, including those of the esophagus. The CDKN2 gene on chromosome 9p21 that encodes the p16 inhibitor of cyclinD/Cdk4 complexes is a target of allelic loss and inactivation in a variety of human cancers and cell lines. However, the roles of 9p21 allelic losses and CDKN2 mutations in human neoplastic progression in vivo remain controversial. We determined the prevalence of allelic loss at 9p21 and mutations in CDKN2 in esophageal adenocarcinomas and investigated the order in which they occurred relative to the development of aneuploidy and cancer during neoplastic progression. Aneuploid cell populations from 32 patients with Barrett's esophagus who had premalignant epithelium, cancer, or both, were purified by DNA content flow cytometric cell sorting and evaluated by polymerase chain reaction. Twenty-four of 32 informative patients (75%) had allelic loss at 9p21 in aneuploid cell populations. Premalignant epithelium was available for seven of the patients who had 9p21 allelic losses in cancer; allelic loss of 9p21 was detected before cancer in all seven (100%). Allelic loss of 9p21 preceded the development of aneuploidy in 13 of 15 patients (87%) who had aneuploid cell populations detected in premalignant epithelium, and the two events were detected simultaneously in the remaining two patients. Five of 22 aneuploid populations (23%) with 9p21 loss had somatic mutations in the remaining CDKN2 allele. The same mutations and 9p21 allelic losses were also found in the corresponding diploid cells from premalignant epithelium in all three cases that were evaluable. However, there was no evidence for mutation or homozygous deletion of p16 in the other 17 patients with 9p21 allelic loss. Our results indicate that 9p21 allelic losses and CDKN2 mutations develop as early lesions in diploid cells before aneuploidy and cancer during neoplastic progression in Barrett's esophagus.

摘要

据报道,9号染色体短臂21区(9p21)的高频等位基因缺失存在于包括食管癌在内的多种人类癌症中。位于9p21的CDKN2基因编码细胞周期蛋白D/细胞周期蛋白依赖性激酶4(Cdk4)复合物的p16抑制剂,在多种人类癌症和细胞系中,该基因是等位基因缺失和失活的靶点。然而,9p21等位基因缺失和CDKN2突变在人类肿瘤体内进展中的作用仍存在争议。我们测定了食管腺癌中9p21等位基因缺失的发生率以及CDKN2的突变情况,并研究了它们相对于非整倍体形成和肿瘤进展过程中癌症发生的先后顺序。通过DNA含量流式细胞术细胞分选,从32例患有Barrett食管且有癌前上皮、癌症或两者皆有的患者中纯化出非整倍体细胞群体,并通过聚合酶链反应进行评估。在32例可提供信息的患者中,有24例(75%)的非整倍体细胞群体存在9p21等位基因缺失。在癌症中存在9p21等位基因缺失的7例患者中有癌前上皮组织;在所有7例患者(100%)中,癌症发生前均检测到9p21等位基因缺失。在15例癌前上皮组织中检测到非整倍体细胞群体的患者中,有13例(87%)9p21等位基因缺失先于非整倍体形成,其余2例患者中这两个事件同时被检测到。在22个存在9p21缺失的非整倍体群体中,有5个(23%)在剩余的CDKN2等位基因中存在体细胞突变。在所有3例可评估的病例中,癌前上皮组织相应的二倍体细胞中也发现了相同的突变和9p21等位基因缺失。然而,在其他17例存在9p21等位基因缺失的患者中,没有证据表明p16发生了突变或纯合缺失。我们的结果表明,在Barrett食管肿瘤进展过程中,9p21等位基因缺失和CDKN2突变作为二倍体细胞中的早期病变,先于非整倍体形成和癌症出现。

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