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Hypoxia-inducible factor-1α correlates with MET and metastasis in node-negative breast cancer

机译:缺氧诱导因子-1α与淋巴结阴性乳腺癌的MET和转移相关

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The mechanism of tumor hypoxia promoting metastasis remains uncertain. Hypoxia-inducible factor-1α (HIF-1α) is a key mediator of the cellular response to hypoxia and binds the met promoter, resulting in increased expression of MET. In breast cancer, MET overexpression is associated with death caused by metastatic disease. Aim of this study is to investigate the role of HIF-1α in MET expression and metastasis in lymph node negative breast cancer. We recruited a homogeneous cohort of 104 patients with T1–2N0M0 breast carcinoma, who had undergone primary surgery. Fifty-three patients had distant metastases and 51 patients had no evidence of disease for more than 10 years. We analyzed the expressions of HIF-1α and MET in these patients using immunohistochemistry. HIF-1α and MET were positively correlated (Spearman’s rank correlation coefficient, 0.35; P < 0.01), were independent predictors of distant metastasis (P = 0.002 and P = 0.03, respectively), and correlated with poor 10-year disease-free survival rate (P < 0.001 for both). Furthermore, co-overexpression of HIF-1α and MET was a significant independent predictor of distant metastasis (odd radio, 10.78; P < 0.001), and patients with co-overexpression had a significantly worse 10-year disease-free survival rate. The results provide evidence that tumor hypoxia promotes metastasis through the induction of MET overexpression by HIF-1α and emphasize the promising status of HIF-1α as a therapeutic target against metastasis in node-negative breast cancer.
机译:肿瘤缺氧促进转移的机制仍不确定。缺氧诱导因子-1α(HIF-1α)是细胞对缺氧反应的关键介体,并与met启动子结合,导致MET表达增加。在乳腺癌中,MET过表达与转移性疾病引起的死亡有关。这项研究的目的是调查HIF-1α在淋巴结阴性乳腺癌的MET表达和转移中的作用。我们招募了104例接受了原发手术的T1–2 N0 M0 乳腺癌患者。 53例患者有远处转移,51例患者在超过10年内无疾病迹象。我们使用免疫组织化学分析了这些患者中HIF-1α和MET的表达。 HIF-1α和MET呈正相关(Spearman等级相关系数为0.35; P <0.01),是远处转移的独立预测因子(分别为P = 0.002和P = 0.03),并且与10年无病生存率相关率(两者均P <0.001)。此外,HIF-1α和MET的共同过度表达是远处转移的重要独立预测因子(奇数射电,10.78; P <0.001),并且共同过度表达的患者10年无病生存率显着降低。结果提供了证据,即肿瘤低氧通过HIF-1α诱导MET过表达促进转移,并强调了HIF-1α作为结节阴性乳腺癌转移靶点的前景。

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