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首页> 外文期刊>American Journal of Pathology: Official Publication of the American Association of Pathologists >Expression of hypoxic marker CA IX is regulated by site-specific DNA methylation and is associated with the histology of gastric cancer.
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Expression of hypoxic marker CA IX is regulated by site-specific DNA methylation and is associated with the histology of gastric cancer.

机译:缺氧标志物CaIx的表达由特异性DNA甲基化调节,与胃癌的组织学相关。

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摘要

The hypoxic marker carbonic anhydrase (CA) IX has been recognized as a tumor-associated protein and is essential for cancer development. However, because CA IX expression does not always correlate with hypoxia, its regulatory mechanism remains unclear. The objective of the present study was to clarify the role and regulation of CA IX expression in gastric cancer. The immunohistochemical expression of CA IX and hypoxia-inducible factor-1alpha was assessed in 77 patients with gastric cancer. A methylation-sensitive restriction enzyme method was used to quantify site-specific methylation at -74 bp in the CA9 promoter in tissue from patients with gastric cancer and in corresponding normal tissue. CA9 expression in cell lines was strongly dependent on methylation status but not hypoxic stimuli. In tissue from patients with gastric cancer, the quantity of methylation was significantly correlated with the protein expression (P = 0.003). Moreover, the methylation value was significantly lower in intestinal-type compared with diffuse-type cancer (P = 0.003). Compared with normal mucosa, intestinal-type cancer demonstrated significant hypomethylation, whereas diffuse-type cancer exhibited hypermethylation. In conclusion, expression of CA IX in gastric cancer is predominantly regulated by methylation of a single CpG rather than by hypoxia. Furthermore, epigenetic alterations in CA9 differ between the intestinal and diffuse types of gastric cancer.
机译:缺氧标志物碳酸酐酶(CA)IX已被认为是肿瘤相关蛋白,对癌症发育至关重要。然而,因为CA IX表达与缺氧并不总是相关,所以其调节机制仍然不清楚。本研究的目的是阐明Ca IX表达在胃癌中的作用和调节。在77例胃癌患者中评估了CaIX和缺氧诱导因子-1Alpha的免疫组化表达。使用甲基化敏感的限制酶方法在来自胃癌和相应的正常组织中的CA9启动子中的CA9启动子中对-74bp的定量特异性甲基化。细胞系中的CA9表达强烈依赖于甲基化状态但不是缺氧刺激。在来自胃癌患者的组织中,甲基化量与蛋白质表达显着相关(p = 0.003)。此外,与弥漫型癌症相比,肠型甲基化值显着降低(P = 0.003)。与正常粘膜相比,肠型癌症表现出显着的低甲基化,而弥漫性癌症表现出高甲基化。总之,Ca IX在胃癌中的表达主要由单个CpG而不是缺氧的甲基化。此外,CA9中的表观遗传改变在肠和弥漫性胃癌之间不同。

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