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瞬时受体电位香草酸亚型 1(TRPV1)和磷酸酶及张力蛋白同源物(PTEN)的联合是宫颈癌的一种有效的预后生物标志物。

The Combination of Transient Receptor Potential Vanilloid Type 1 (TRPV1) and Phosphatase and Tension Homolog (PTEN) is an Effective Prognostic Biomarker in Cervical Cancer.

出版信息

Int J Gynecol Pathol. 2021 May 1;40(3):214-223. doi: 10.1097/PGP.0000000000000677.

Abstract

Transient receptor potential vanilloid type 1 (TRPV1) has been reported to play an important role in human cancers. However, the knowledge about TRPV1 in cervical cancer is sparse. Therefore, we evaluated the expression and clinical significance of TRPV1 in cervical cancer. Immunohistochemical analyses were performed for TRPV1 and phosphatase and tension homolog (PTEN) to delineate clinical significance using 150 cervical cancers, 230 cervical intraepithelial neoplasias, and 312 normal cervical epithelial tissues in a tissue microarray. Furthermore, the role of TRPV1 in cell growth was assessed in a cervical cancer cell line. The TRPV1 expression was significantly higher in cervical cancer tissues than in cervical intraepithelial neoplasias, and normal epithelial tissues (P<0.001). In cervical cancer tissues, TRPV1 expression negatively correlated with PTEN expression (Spearman ρ=-0.121, P=0.009). Multivariate survival analysis revealed high TRPV1 expression (hazard ratio=3.41, 95% confidence interval: 1.25-9.27, P=0.016) as an independent prognostic factor for overall survival. Notably. the high TRPV1/low PTEN expression showed the highest hazard ratio (5.87; 95% confidence interval: 2.18-15.82, P<0.001) for overall survival. In vitro results demonstrated that the overexpression of TRPV1 was associated with increased cell viability and colony formation. Overexpression of TRPV1 could be a good biomarker for the prediction of chemoradiation response. Our result suggested promising potential of high TRPV1/low PTEN as prognostic and survival makers. The possible link between the biologic function of TRPV1 and PTEN in cervical cancer warrants further studies.

摘要

瞬时受体电位香草酸亚型 1(TRPV1)已被报道在人类癌症中发挥重要作用。然而,关于宫颈癌中 TRPV1 的知识还很匮乏。因此,我们评估了 TRPV1 在宫颈癌中的表达及其临床意义。使用组织微阵列,对 150 例宫颈癌、230 例宫颈上皮内瘤变和 312 例正常宫颈上皮组织进行 TRPV1 和磷酸酶张力蛋白同源物(PTEN)的免疫组织化学分析,以阐明其临床意义。此外,还在宫颈癌细胞系中评估了 TRPV1 在细胞生长中的作用。TRPV1 在宫颈癌组织中的表达明显高于宫颈上皮内瘤变和正常上皮组织(P<0.001)。在宫颈癌组织中,TRPV1 表达与 PTEN 表达呈负相关(Spearman ρ=-0.121,P=0.009)。多变量生存分析显示,高 TRPV1 表达(危险比=3.41,95%置信区间:1.25-9.27,P=0.016)是总生存期的独立预后因素。值得注意的是,高 TRPV1/低 PTEN 表达的总生存期的危险比最高(5.87;95%置信区间:2.18-15.82,P<0.001)。体外结果表明,TRPV1 的过表达与细胞活力和集落形成增加有关。TRPV1 的过表达可能是预测放化疗反应的一个很好的生物标志物。我们的结果表明,TRPV1 高/PTEN 低具有作为预后和生存标志物的潜在前景。TRPV1 和 PTEN 在宫颈癌中的生物学功能之间的可能联系值得进一步研究。

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