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脯氨酰羟化酶 2 表达低下与结直肠癌患者的肿瘤分级和预后不良相关。

Low expression of prolyl hydroxylase 2 is associated with tumor grade and poor prognosis in patients with colorectal cancer.

机构信息

Department of Oncology, Southwest Hospital, Third Military Medical University, Chongqing 400038, China.

出版信息

Exp Biol Med (Maywood). 2012 Jul;237(7):860-6. doi: 10.1258/ebm.2012.011331. Epub 2012 Jul 16.

Abstract

Previous studies have indicated that prolyl hydroxylases (PHDs) function as tumor suppressors in human colorectal cancer (CRC), but their clinical and prognostic significance is uncertain. Expressions of PHD1, PHD2, PHD3 and hypoxia-inducible factor (HIF)-1α were detected using immunohistochemistry in an independent CRC cohort of 93 specimens represented on a tissue microarray (TMA). PHD expression levels were correlated with clinicopathological features, patient survival and presumed corresponding HIF-1α expression. Pearson χ(2) test was used to compare clinicopathological features with protein expressions. Survival was estimated by Kaplan-Meier analysis. Cox regression analysis was performed for multivariate analysis of prognostic factors. Of the TMA, 47, 68 and 51 from 93 specimens had low expressions of PHD1, PHD2 and PHD3, respectively. HIF-1α was positively expressed in 75 specimens. Low expression of PHD2 correlated with the high-grade group and a terrible overall survival (P = 0.017 and P = 0.032). Patients who had early stage CRC with low PHD2 expression had a poorer survival (P = 0.015), whereas patients with advanced-stage disease did not demonstrate such a difference (P = 0.691). Besides, PHD2 was uncorrelated with HIF-1α expression. The present study indicated that low expression of PHD2 in CRC predicts poor survival independent of HIF-1α, specifically for patients who have early stage tumors.

摘要

先前的研究表明脯氨酰羟化酶(PHD)在人结直肠癌(CRC)中作为肿瘤抑制因子发挥作用,但它们的临床和预后意义尚不确定。使用免疫组织化学法在独立的 CRC 队列中检测了 93 个组织微阵列(TMA)标本中的 PHD1、PHD2、PHD3 和缺氧诱导因子(HIF)-1α的表达。PHD 表达水平与临床病理特征、患者生存和推测的相应 HIF-1α表达相关。使用 Pearson χ(2)检验比较临床病理特征与蛋白表达。通过 Kaplan-Meier 分析估计生存情况。对预后因素进行 Cox 回归分析。在 TMA 中,93 个标本中的 47、68 和 51 个标本的 PHD1、PHD2 和 PHD3 表达水平较低。75 个标本 HIF-1α呈阳性表达。PHD2 低表达与高级别组和总生存率差相关(P = 0.017 和 P = 0.032)。PHD2 低表达的早期 CRC 患者生存较差(P = 0.015),而晚期疾病患者则无此差异(P = 0.691)。此外,PHD2 与 HIF-1α表达无关。本研究表明,CRC 中 PHD2 的低表达独立于 HIF-1α预测预后不良,特别是对于早期肿瘤患者。

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