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Cyclooxygenase-1 and cyclooxygenase-2 gene expression in human colorectal adenocarcinomas and in azoxymethane induced colonic tumours in rats.

机译:环氧合酶-1和环氧合酶-2基因在大肠腺癌和乙氧基甲烷诱导的大鼠结肠肿瘤中的表达。

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摘要

Increased prostaglandin E2 synthesis is considered important in both human and experimental colon carcinogenesis. It is not known, however, which cyclooxygenase isoenzyme is involved. The aim of this study was to compare the content of mRNA for cyclooxygenase-1 and cyclooxygenase-2 in colorectal cancers with the content in normal colonic specimens. Fifteen human colorectal adenocarcinomas, 35 azoxymethane induced colonic tumours from rats, and specimens of normal colon were analysed by reverse transcription and polymerase chain reaction (RT-PCR). It was found that cyclooxygenase-1 and cyclooxygenase-2 mRNA were increased in azoxymethane induced colonic tumours, compared with specimens taken adjacent to the tumours or from the macroscopically normal intestine distant from the tumours. Cyclooxygenase-1 and cyclooxygenase-2 mRNA were increased in specimens from the macroscopically normal intestine of azoxymethane treated animals, compared with colonic specimens from saline treated rats. Cyclooxygenase-2 mRNA, but not cyclooxygenase-1 mRNA, was increased in human colorectal cancers, compared with the adjacent mucosa or macroscopically normal mucosa distant from the tumours. The results suggest that cyclooxygenase-2 is involved in the increased prostaglandin E2 synthesis in colonic cancers, and that activation of this isoenzyme is an early event in colon carcinogenesis. However, cyclooxygenase-1 may also be involved, at least in experimental colon carcinogenesis.
机译:前列腺素E2合成的增加在人类和实验性结肠癌的发生中均被认为是重要的。然而,不知道涉及哪种环氧合酶同工酶。这项研究的目的是比较大肠癌中环氧合酶1和环氧合酶2的mRNA含量与正常结肠标本中的含量。通过逆转录和聚合酶链反应(RT-PCR)分析了15例人类大肠腺癌,35株甲氧基甲烷诱导的大鼠结肠癌和正常结肠标本。研究发现,与邻近肿瘤或从远离肿瘤的宏观正常肠道中采集的标本相比,在由乙氧基甲烷诱导的结肠肿瘤中,环氧合酶-1和环氧合酶-2的mRNA增加。与用盐水处理的大鼠的结肠标本相比,用乙氧甲烷处理的动物的宏观正常肠道中的标本中的环氧合酶-1和环氧合酶-2的mRNA增加。与相邻的粘膜或远离肿瘤的肉眼可见的正常粘膜相比,人结肠直肠癌中的环氧合酶-2 mRNA增加,而环氧合酶-1 mRNA没有增加。结果表明,环氧合酶2参与了结肠癌中前列腺素E2合成的增加,并且这种同工酶的激活是结肠癌发生的早期事件。然而,至少在实验性结肠癌的发生中,环氧合酶-1也可能参与。

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