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P2Y嘌呤受体介导的信号传导系统在前列腺癌细胞生长及转移中的作用 被引量:3

P2Y purinoceptor-mediated signal transduction pathway in regulation of growth and metastasis of prostate carcinoma
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摘要 The most frequent cause of death for cancer patients is metastasis. The precise molecular events leading to the acquisition of malignant phenotypes remain largely unknown. During the past 10 years, we have focused our efforts on exploring signaling mechanisms underlying malignant progression of human prostate carcinoma. We found that activation of P2Y purinoceptor on androgen independent prostate carcinoma cell lines resulted in significant growth inhibition. This growth inhibitory effect was accompanied by activation of phospholipase C and calcium mobilization, and proved receptor specific. We also demonstrated that the G protein coupled P2Y purinoceptor was linked to Erk1/2 and p38 MAPK pathway, and there existed cross talk between phospholipase C and MAPK pathways. We found Erk1/2 and p38 MAPK pathways were differentially activated between metastatic and non metastatic prostate carcinoma cell subclones, providing valuable clue to further study molecular mechanism of tumor metastasis. The most frequent cause of death for cancer patients is metastasis. The precise molecular events leading to the acquisition of malignant phenotypes remain largely unknown. During the past 10 years, we have focused our efforts on exploring signaling mechanisms underlying malignant progression of human prostate carcinoma. We found that activation of P2Y purinoceptor on androgen independent prostate carcinoma cell lines resulted in significant growth inhibition. This growth inhibitory effect was accompanied by activation of phospholipase C and calcium mobilization, and proved receptor specific. We also demonstrated that the G protein coupled P2Y purinoceptor was linked to Erk1/2 and p38 MAPK pathway, and there existed cross talk between phospholipase C and MAPK pathways. We found Erk1/2 and p38 MAPK pathways were differentially activated between metastatic and non metastatic prostate carcinoma cell subclones, providing valuable clue to further study molecular mechanism of tumor metastasis.
出处 《北京大学学报(医学版)》 CAS CSCD 北大核心 2001年第5期394-397,共4页 Journal of Peking University:Health Sciences
基金 国家自然科学基金 ( 392 0 0 14 2 ) ( 30 0 70 2 93) 北京市自然科学基金 ( 70 0 2 0 2 2 )资助~~
关键词 P2Y嘌呤 信号传递 前列腺肿瘤 遗传学 肿瘤转移 前列腺癌 细胞生长 Signal transduction/genet Prostatic neoplasms/genet Neoplasm metastasis/genet
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