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将 PKC-α、CDK6 和 MET 定义为三阴性乳腺癌的治疗靶点。

Definition of PKC-α, CDK6, and MET as therapeutic targets in triple-negative breast cancer.

机构信息

Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas. The University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas.

出版信息

Cancer Res. 2014 Sep 1;74(17):4822-35. doi: 10.1158/0008-5472.CAN-14-0584. Epub 2014 Jun 26.

Abstract

Triple-negative breast cancer (TNBC) is a highly heterogeneous and recurrent subtype of breast cancer that lacks an effective targeted therapy. To identify candidate therapeutic targets, we profiled global gene expression in TNBC and breast tumor-initiating cells with a patient survival dataset. Eight TNBC-related kinases were found to be overexpressed in TNBC cells with stem-like properties. Among them, expression of PKC-α, MET, and CDK6 correlated with poorer survival outcomes. In cases coexpressing two of these three kinases, survival rates were lower than in cases where only one of these kinases was expressed. In functional tests, two-drug combinations targeting these three kinases inhibited TNBC cell proliferation and tumorigenic potential in a cooperative manner. A combination of PKC-α-MET inhibitors also attenuated tumor growth in a cooperative manner in vivo. Our findings define three kinases critical for TNBC growth and offer a preclinical rationale for their candidacy as effective therapeutic targets in treating TNBC.

摘要

三阴性乳腺癌(TNBC)是一种高度异质性和复发性的乳腺癌亚型,缺乏有效的靶向治疗方法。为了确定候选治疗靶点,我们对具有患者生存数据的 TNBC 和乳腺癌起始细胞进行了全基因表达谱分析。结果发现,八种与 TNBC 相关的激酶在具有干细胞样特性的 TNBC 细胞中过表达。其中,PKC-α、MET 和 CDK6 的表达与较差的生存结果相关。在这三种激酶中两种共表达的情况下,生存率低于仅表达一种激酶的情况。在功能测试中,针对这三种激酶的两种药物联合以协同方式抑制 TNBC 细胞的增殖和致瘤潜能。PKC-α-MET 抑制剂的联合也以协同方式在体内减轻肿瘤生长。我们的研究结果定义了三种对 TNBC 生长至关重要的激酶,并为它们作为治疗 TNBC 的有效治疗靶点的候选提供了临床前依据。

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