首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >PROSTAGLANDIN H SYNTHASE 2 IS EXPRESSED ABNORMALLY IN HUMAN COLON CANCER - EVIDENCE FOR A TRANSCRIPTIONAL EFFECT
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PROSTAGLANDIN H SYNTHASE 2 IS EXPRESSED ABNORMALLY IN HUMAN COLON CANCER - EVIDENCE FOR A TRANSCRIPTIONAL EFFECT

机译:前列腺素H合酶2在人类结肠癌中异常表达-证明有转录作用

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Evidence from epidemiological studies, clinical trials, and animal experiments indicates that inhibitors of prostaglandin synthesis lower the risk of colon cancer. We tested the hypothesis that abnormal expression of prostaglandin H synthase 2 (PHS-2), which can be induced by oncogenes and tumor promoters, occurs during colon carcinogenesis by examining its level in colon tumors. Human colon cancers were found to have an increased expression of PHS-2 mRNA compared with normal colon specimens from the same patient (n = 5). In situ hybridization showed that the neoplastic colonocytes had increased expression of PHS-2 (n = 4). Additionally, five colon cancer cell lines were shown to express high levels of PHS-2 mRNA even in the absence of a known inducer of PHS-2. To study the basis for this increased gene expression, we transfected a colon cancer cell line, HCT-116, with a reporter gene containing 2.0 kb of the 5' regulatory sequence of the PHS-2 gene. Constitutive transcription of the reporter gene was observed, whereas normal control cell lines transcribed the reporter only in response to an exogenous agonist. We conclude that PHS-2 is transcribed abnormally in human colon cancers and that this may be one mechanism by which prostaglandins or related compounds that support carcinogenesis are generated. [References: 36]
机译:流行病学研究,临床试验和动物实验的证据表明,前列腺素合成抑制剂可降低结肠癌的风险。我们通过检查结肠癌的水平,检验了癌基因和肿瘤启动子诱导的前列腺素H合酶2(PHS-2)异常表达的假说。与来自同一患者的正常结肠标本相比,发现人类结肠癌的PHS-2 mRNA表达增加(n = 5)。原位杂交表明,肿瘤结肠细胞的PHS-2表达增加(n = 4)。另外,即使在没有已知的PHS-2诱导剂的情况下,五个结肠癌细胞系也显示出高水平的PHS-2 mRNA。为了研究这种基因表达增加的基础,我们用含有2.0 kb PHS-2基因5'调控序列的报告基因转染了结肠癌细胞HCT-116。观察到报告基因的组成性转录,而正常对照细胞系仅响应于外源激动剂才转录报告基因。我们得出结论,PHS-2在人类结肠癌中异常转录,这可能是前列腺素或支持癌变的相关化合物生成的一种机制。 [参考:36]

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