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首页> 外文期刊>Acta medica Okayama >HIF-1α Contributes to Hypoxia-induced Invasion and Metastasis of Esophageal Carcinoma via Inhibiting E-cadherin and Promoting MMP-2 Expression
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HIF-1α Contributes to Hypoxia-induced Invasion and Metastasis of Esophageal Carcinoma via Inhibiting E-cadherin and Promoting MMP-2 Expression

机译:HIF-1α通过抑制E-钙黏着蛋白和促进MMP-2表达促进缺氧诱导的食管癌浸润和转移

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摘要

Hypoxia-inducible factor-1α (HIF-1α) has been found to enhance tumor invasion and metastasis, but no study has reported its action in esophageal carcinoma. The goal of this study was to explore the probable mechanism of HIF-1α in the invasion and metastasis of esophageal carcinoma Eca109 cells in vitro and in vivo. mRNA and protein expression of HIF-1α, E-cadherin and matrix metalloproteinase-2 (MMP-2) under hypoxia were detected by RT-PCR and Western blotting. The effects of silencing HIF-1α on E-cadherin, MMP-2 mRNA and protein expression under hypoxia or normoxia were detected by RT-PCR and Western blotting, respectively. The invasive ability of Eca109 cells was tested using a transwell chambers. We established an Eca109-implanted tumor model and observed tumor growth and lymph node metastasis. The expression of HIF-1α, E-cadherin and MMP-2 in xenograft tumors was detected by Western blotting. After exposure to hypoxia, HIF-1α protein was up-regulated, both mRNA and protein levels of E-cadherin were down-regulated and MMP-2 was up-regulated, while HIF-1α mRNA showed no significant change. SiRNA could block HIF-1α effectively, increase E-cadherin expression and inhibit MMP-2 expression. The number of invading cells decreased after HIF-1α was silenced. Meanwhile, the tumor volume was much smaller, and the metastatic rate of lymph nodes and the positive rate were lower in vivo. Our observations suggest that HIF-1α inhibition might be an effective strategy to weaken invasion and metastasis in the esophageal carcinoma Eca109 cell line.
机译:缺氧诱导因子-1α(HIF-1α)被发现可以增强肿瘤的侵袭和转移能力,但尚无研究报道其在食管癌中的作用。这项研究的目的是探讨HIF-1α在食管癌Eca109细胞体外和体内侵袭和转移的可能机制。通过RT-PCR和Western blotting检测缺氧条件下HIF-1α,E-cadherin和基质金属蛋白酶-2(MMP-2)的mRNA和蛋白表达。分别通过RT-PCR和Western blotting检测HIF-1α沉默对缺氧或常氧条件下E-cadherin,MMP-2 mRNA和蛋白表达的影响。使用transwell小室测试Eca109细胞的侵袭能力。我们建立了一个植入Eca109的肿瘤模型,并观察了肿瘤的生长和淋巴结转移。 Western blot检测HIF-1α,E-cadherin和MMP-2在异种移植肿瘤中的表达。暴露于缺氧条件下,HIF-1α蛋白上调,E-cadherin mRNA和蛋白水平下调,MMP-2上调,而HIF-1αmRNA无明显变化。 SiRNA可以有效地阻断HIF-1α,增加E-钙粘蛋白的表达并抑制MMP-2的表达。 HIF-1α沉默后,侵袭细胞的数量减少。同时,体内肿瘤体积小得多,淋巴结转移率和阳性率较低。我们的观察结果表明,抑制HIF-1α可能是减弱食管癌Eca109细胞系侵袭和转移的有效策略。

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