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Re: GPRC6A Regulates Prostate Cancer Progression

机译:回复:GPRC6A调节前列腺癌的进展

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Background: GPRC6A is a nutrient sensing GPCR that is activated in vitro by a variety of ligands, including amino acids, calcium, zinc, osteocalcin (OC), and testosterone. The association between nutritional factors and risk of prostate cancer, the finding of increased expression of OC in prostate cancer cells, and the association between GPRC6A and risk of prostate cancer in Japanese men implicates a role of GPRC6A in prostate cancer. Methods: We examined if GPRC6A is expressed in human prostate cancer cell lines and used siRNA-mediated knockdown GPRC6A expression in prostate cancer cells to explore the function of GPRC6A in vitro. To assess the role of GPRC6A in prostate cancer progression in vivo, we intercrossed Gprc6a(-/-) mice onto the TRAMP mouse prostate cancer model. Results: GPRC6A transcripts were markedly increased in prostate cancer cell lines 22Rvl, PC-3, and LNCaP, compared to the normal prostate RWPE-1 cell line. In addition, a panel of GPRC6A ligands, including calcium, OC, and arginine, exhibited in prostate cancer cell lines a dose-dependent stimulation of ERK activity, cell proliferation, chemotaxis, and prostate specific antigen and Runx2 gene expression. These responses were inhibited by siRNA-mediated knockdown of GPRC6A. Finally, transfer of Gprc6a deficiency onto a TRAMP mouse model of prostate cancer significantly retarded prostate cancer progression and improved survival of compound Gprc6a(—/—)/TRAMP mice. Conclusions: GPRC6A is a novel molecular target for regulating prostate growth and cancer progression. Increments in GPRC6A may augment the ability of prostate cancer cells to proliferate in response to dietary and bone derived ligands.
机译:背景:GPRC6A是一种营养敏感的GPCR,可在体外被多种配体激活,包括氨基酸,钙,锌,骨钙素(OC)和睾丸激素。营养因子与前列腺癌风险之间的关联,在前列腺癌细胞中OC表达增加的发现以及GPRC6A与日本男性前列腺癌风险之间的关联暗示GPRC6A在前列腺癌中的作用。方法:我们检查了GPRC6A是否在人前列腺癌细胞系中表达,并使用siRNA介导的敲低GPRC6A在前列腺癌细胞中的表达来探索GPRC6A的体外功能。若要评估GPRC6A在体内前列腺癌进展中的作用,我们将Gprc6a(-/-)小鼠交配到TRAMP小鼠前列腺癌模型上。结果:与正常前列腺RWPE-1细胞系相比,前列腺癌细胞系22Rv1,PC-3和LNCaP中的GPRC6A转录物显着增加。此外,一组GPRC6A配体(包括钙,OC和精氨酸)在前列腺癌细胞系中表现出剂量依赖性的ERK活性,细胞增殖,趋化性以及前列腺特异抗原和Runx2基因表达的刺激。 siRNA介导的GPRC6A的敲低抑制了这些反应。最后,将Gprc6a缺乏症转移至前列腺癌的TRAMP小鼠模型上可显着延缓前列腺癌的进展并提高化合物Gprc6a(-/-)/ TRAMP小鼠的存活率。结论:GPRC6A是调节前列腺生长和癌症进展的新型分子靶标。 GPRC6A的增加可能会增强前列腺癌细胞响应饮食和骨骼衍生的配体而增殖的能力。

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