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参与肺癌和结直肠癌转移的肿瘤抑制基因。

Tumor suppressor genes involved in metastasis of lung and colorectal carcinomas.

作者信息

Yokota J, Ookawa K, Nishikawa R, Sameshima Y

机构信息

Section of Studies on Metastasis, National Cancer Center Research Institute, Tokyo, Japan.

出版信息

Princess Takamatsu Symp. 1991;22:71-6.

PMID:1844253
Abstract

Inactivation of tumor suppressor genes is now believed to play an important role in various progression stages of human cancers. To clarify the possible involvement of tumor suppressor gene inactivation in the acquisition of metastatic potential in lung and colorectal carcinoma cells, we examined various genetic alterations in both primary tumors and metastases obtained from patients with lung and colorectal carcinomas. In lung carcinoma, loss of heterozygosity on chromosomes 3p, 13q, and 17p is a common genetic alteration, and both RB and p53 genes are inactivated as a result of chromosome 13q and 17p losses. In some cases, allelic loss on chromosome 11p and amplification of myc family oncogenes occur during tumor progression. In colorectal carcinoma, p53 and DCC alterations were detected in 100% of metastases, and sequential accumulation of allelic losses on chromosomes 13q, 14q, and 18q in the process of metastasis was observed. These results indicate that a subset of tumor suppressor genes is involved in metastasis of lung and colorectal carcinomas.

摘要

目前认为肿瘤抑制基因的失活在人类癌症的各个进展阶段中发挥着重要作用。为了阐明肿瘤抑制基因失活在肺癌和结肠癌细胞转移潜能获得过程中可能的参与情况,我们检测了从肺癌和结肠癌患者获取的原发性肿瘤和转移灶中的各种基因改变。在肺癌中,3p、13q和17p染色体上的杂合性缺失是常见的基因改变,并且RB和p53基因由于13q和17p染色体缺失而失活。在某些情况下,在肿瘤进展过程中会出现11p染色体上等位基因缺失和myc家族癌基因的扩增。在结肠癌中,在100%的转移灶中检测到p53和DCC改变,并且在转移过程中观察到13q、14q和18q染色体上等位基因缺失的顺序累积。这些结果表明,一部分肿瘤抑制基因参与了肺癌和结肠癌的转移。

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