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人胃癌细胞系、胃黏膜及癌组织中未检测到重排的Tpr-met mRNA表达。

Lack of rearranged Tpr-met mRNA expression in human gastric cancer cell lines and gastric mucosa and carcinoma.

作者信息

Osaki M, Miyata H, Hayashi A, Gomyo Y, Tatebe S, Ito H

机构信息

First Department of Pathology, Faculty of Medicine, Tottori University, Yonago, Japan.

出版信息

Anticancer Res. 1996 Sep-Oct;16(5A):2881-4.

PMID:8917402
Abstract

The met protooncogene was activated by a rearrangement involving the fusion of tpr (1q25) and met (7q21-31) gene sequence in a human osteosarcoma cell line (HOS) incubated in vitro with N-methyl-N-nitro-N-nitrosoguanidine (MNNG). We examined the expression of tpr-met mRNA by means of the reverse transcription-nested polymerase chain reaction (RT-nested PCR) in human two gastric cell lines (MKN-1 and MKN-45), T-cell acute lymphocytic leukemia cell line (MOLT-4), and in gastric tissue samples including normal mucosa, intestinal metaplasia and carcinoma from three surgical specimens. A DNA fragment of 88-bp was amplified in MKN-1 and MOLT-4, 96-bp in MKN-45 and of 58-bp in all nine tissue samples including gastric carcinomas. The amplified DNA sequences were not homologous with the rearranged tpr-met gene. Our study indicated that rearranged tpr-met mRNA is not expressed either in human gastric carcinoma cell lines or in gastric mucosa and carcinoma.

摘要

在体外用人骨肉瘤细胞系(HOS)与N-甲基-N-硝基-N-亚硝基胍(MNNG)孵育时,原癌基因met通过涉及tpr(1q25)和met(7q21 - 31)基因序列融合的重排而被激活。我们通过逆转录巢式聚合酶链反应(RT - 巢式PCR)检测了人两种胃癌细胞系(MKN - 1和MKN - 45)、T细胞急性淋巴细胞白血病细胞系(MOLT - 4)以及包括来自三个手术标本的正常黏膜、肠化生和癌的胃组织样本中tpr - met mRNA的表达。在MKN - 1和MOLT - 4中扩增出一个88 bp的DNA片段,在MKN - 45中扩增出96 bp的片段,在包括胃癌在内的所有九个组织样本中扩增出58 bp的片段。扩增的DNA序列与重排的tpr - met基因不同源。我们的研究表明,重排的tpr - met mRNA在人胃癌细胞系或胃黏膜及癌中均未表达。

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