α 1-肾上腺素受体(ñ1-AR)和瞬时受体电位(TRP)之间的协同相互作用触发前列腺癌细胞系的增殖细胞信号

G. Santoni, M. Morelli, C. Amantini, M. Santoni, M. Nabissi, C. Cardinali, F. Bello, Aless, R. Piergentili, W. Quaglia
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引用次数: 3

摘要

钙(Ca2+)增加了人类晚期前列腺癌(PCa)细胞的增殖,但涉及的离子通道尚不清楚。Santoni组和Quaglia组研究了PCa细胞中α 1d -肾上腺素能受体(α1D-AR)与瞬时受体电位香草样蛋白1 (TRPV1)离子通道表达的相关性。与BPH相比,PCa中α1D-AR和TRPV1 mrna升高。α1D-AR和TRPV1在PCa细胞中共表达。去甲肾上腺素(NE)诱导α1D-AR-和trpv1依赖的质子释放、PC3细胞内Ca2+的流动以及PLC、PKC和ERK通路的激活,从而刺激PC3细胞的增殖。同样,TRPC6或GPR55在系膜细胞和前列腺癌细胞α1- ar依赖性增殖中的作用也有报道。总的来说,α - 1- ar和TRPs之间的串扰在PCa细胞中参与了细胞增殖的控制。这些数据有力地促进了α - 1- ar和TRP通道靶向治疗PCa的新药理学方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cooperative Interaction between the Alpha1-Adrenoceptors (ñ1-AR) andTransient Receptor Potential (TRP) Triggers a Proliferative Cell Signal inProstate Cancer Cell Lines
Calcium (Ca2+) increases the proliferation of human advanced prostate cancer (PCa) cells but the ion channels involved are unknown. Santoni and Quaglia groups investigated the correlation between alpha1D-adrenergic receptor (α1D-AR) and the transient receptor potential vanilloid type 1 (TRPV1) ion channel expression in PCa cells. The α1D-AR and TRPV1 mRNAs are increased in PCa compared to BPH. α1D-AR and TRPV1 are co-expressed in PCa cells. Norepinephrine (NE) induced α1D-AR- and TRPV1-dependent protons release, Ca2+ flux in PC3 cells and activation of PLC, PKC and ERK path-ways that stimulated PC3 cell proliferation. Similarly, a role for TRPC6 or GPR55 in α1-AR-dependent proliferation of mesangial cells and PCa cells was reported. Overall, a crosstalk between α1-AR and TRPs in PCa cells, involved in the control of cell proliferation has been demonstrated. These data strongly promote a putative novel pharmacological approach in the treatment of PCa by targeting both α1-AR and TRP channels.
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