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蛋白激酶C-α介导人前列腺癌细胞中表皮生长因子受体的反式激活。

Protein kinase C-{alpha} mediates epidermal growth factor receptor transactivation in human prostate cancer cells.

作者信息

Stewart Jubilee R, O'Brian Catherine A

机构信息

Department of Cancer Biology, The University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Box 173, Houston, TX 77030, USA.

出版信息

Mol Cancer Ther. 2005 May;4(5):726-32. doi: 10.1158/1535-7163.MCT-05-0013.

Abstract

Progression of human prostate cancer to a malignancy that is refractory to androgen-ablation therapy renders the disease resistant to available treatment options and accounts for the high prostate cancer mortality rate. Epidermal growth factor receptor (EGFR) expression in human prostate cancer specimens increases with disease progression to androgen-refractory prostate cancer, and experimental models implicate EGFR-dependent signaling to Erk1/2 activation in the androgen-refractory prostate cancer phenotype. 12-O-Tetradecanoylphorbol-13-acetate (TPA)-induced Erk1/2 activation in human prostate cancer PC-3 cells is a paradigm of diacylglycerol-induced EGFR transactivation in androgen-independent prostate cancer. In this report, we establish an obligatory role for TPA-induced protein kinase C (PKC)-alpha activation in EGFR transactivation and signaling to Erk1/2 activation in PC-3 cells. TPA-regulated molecules include PKCs, PKDs, and Ras guanyl nucleotide-releasing proteins. The PKC-selective inhibitors GF109203X and Go6983 each blocked TPA-induced EGFR transactivation, indicating a requirement for PKC. PC-3 cells express four PKC isozymes. Prolonged bryostatin 1 treatment abrogated PKCalpha expression without altering expression levels of the other PKC isozymes. Pharmacologic PKCalpha "knockdown" abrogated TPA-induced Erk1/2 activation without affecting the EGF/EGFR-induced response, indicating that PKCalpha was required for EGFR transactivation but dispensable for signaling of ligand-activated EGFR to Erk1/2 activation. We corroborated this by showing that Go6976, which is a PKCalpha-selective inhibitor in PC-3 cells, likewise abolished TPA-induced Erk1/2 activation and did not inhibit EGF/EGFR-induced Erk1/2 activation. Go6976 had similar effects in DU145 cells, providing evidence for a common PKCalpha-dependent Erk1/2 activation mechanism in androgen-independent human prostate cancer cells of distinct genetic origin. These results constitute a rational basis for selective PKCalpha inhibition as a modality of prostate cancer therapy.

摘要

人类前列腺癌进展为对雄激素剥夺疗法难治的恶性肿瘤,使得该疾病对现有治疗方案产生抗性,并导致前列腺癌死亡率居高不下。在人类前列腺癌标本中,表皮生长因子受体(EGFR)的表达随着疾病进展至雄激素难治性前列腺癌而增加,并且实验模型表明在雄激素难治性前列腺癌表型中,EGFR依赖性信号传导导致Erk1/2激活。12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)诱导人前列腺癌PC - 3细胞中的Erk1/2激活,是雄激素非依赖性前列腺癌中甘油二酯诱导的EGFR转活化的范例。在本报告中,我们确立了TPA诱导的蛋白激酶C(PKC)-α激活在PC - 3细胞中EGFR转活化以及向Erk1/2激活的信号传导中的必要作用。TPA调节的分子包括PKC、PKD和Ras鸟苷核苷酸释放蛋白。PKC选择性抑制剂GF109203X和Go6983均阻断TPA诱导的EGFR转活化,表明需要PKC。PC - 3细胞表达四种PKC同工酶。延长苔藓抑素1处理可消除PKCα的表达,而不改变其他PKC同工酶的表达水平。药理学上的PKCα“敲低”消除了TPA诱导的Erk1/2激活,而不影响EGF/EGFR诱导的反应,表明PKCα是EGFR转活化所必需的,但对于配体激活的EGFR向Erk1/2激活的信号传导是可有可无的。我们通过显示Go6976(PC - 3细胞中的PKCα选择性抑制剂)同样消除TPA诱导的Erk1/2激活且不抑制EGF/EGFR诱导的Erk1/2激活来证实了这一点。Go6976在DU145细胞中具有类似作用,为不同遗传起源的雄激素非依赖性人前列腺癌细胞中常见的PKCα依赖性Erk1/2激活机制提供了证据。这些结果构成了选择性抑制PKCα作为前列腺癌治疗方式的合理基础。

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