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GPR171表达增强肺癌细胞的增殖和转移。

GPR171 expression enhances proliferation and metastasis of lung cancer cells.

作者信息

Dho So Hee, Lee Kwang-Pyo, Jeong Dongjun, Kim Chang-Jin, Chung Kyung-Sook, Kim Ji Young, Park Bum-Chan, Park Sung Sup, Kim Seon-Young, Kwon Ki-Sun

机构信息

Aging Research Institute, Korea Research Institute of Bioscience and Biotechnology, Daejeon 305-806, Republic of Korea.

Radioisotope Research Division, Department of Research Reactor Utilization, Korea Atomic Energy Research Institute, Daejeon 305-353, Republic of Korea.

出版信息

Oncotarget. 2016 Feb 16;7(7):7856-65. doi: 10.18632/oncotarget.6856.

Abstract

G protein-coupled receptors (GPCRs) are among the most significant therapeutic targets and some of them promote the growth and metastasis of cancer. Here, we show that an increase in the levels of GPR171 is crucial for lung cancer tumor progression in vitro and in vivo. Immunostaining of clinical samples indicated that GPR171 was overexpressed in 46.8% of lung carcinoma tissues. Depletion of GPR171 with an anti-GPR171 antibody decreased proliferation of lung carcinoma cells and attenuated tumor progression in a mouse xenograft model. Knockdown of GPR171 also inhibited migration and invasion of the lung cancer cell lines. Notably, inhibition of GPR171 synergistically enhanced the tumoricidal activity of an epidermal growth factor receptor (EGFR) inhibitor in lung cancer cells. These results indicate that GPR171 blockade is a promising antineoplastic strategy and provide a preclinical rationale for combined inhibition of GPR171 and EGFR.

摘要

G蛋白偶联受体(GPCRs)是最重要的治疗靶点之一,其中一些会促进癌症的生长和转移。在此,我们表明GPR171水平的升高对于肺癌在体外和体内的肿瘤进展至关重要。临床样本的免疫染色表明,46.8%的肺癌组织中GPR171过表达。用抗GPR171抗体耗尽GPR171可降低肺癌细胞的增殖,并在小鼠异种移植模型中减弱肿瘤进展。敲低GPR171也抑制肺癌细胞系的迁移和侵袭。值得注意的是,抑制GPR171可协同增强表皮生长因子受体(EGFR)抑制剂在肺癌细胞中的杀瘤活性。这些结果表明,阻断GPR171是一种有前景的抗肿瘤策略,并为联合抑制GPR171和EGFR提供了临床前理论依据。

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