靶向干细胞蛋白BMI1的研究一种潜在的前列腺癌治疗方法

Firdous H Beigh, N. Syeed, M. Maqbool, Rita Singh Majumdhar
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引用次数: 0

摘要

前列腺癌(CaP)因其对常规治疗的耐药性而被认为是临床管理的一个令人烦恼的挑战,导致该疾病的大多数死亡。目前包括去势在内的治疗方案效果甚微,因为大多数患者会产生耐药性并复发为更具侵袭性的去势抵抗性前列腺癌(CRPC)。BMI1 (B细胞特异性Moloney小鼠白血病病毒整合位点1)是polycomb基因家族的致癌成员,也是一种转录抑制因子,在增殖、分化、衰老和干细胞更新等许多过程中发挥关键调节作用。越来越多的证据也揭示了BMI1表达与大多数人类恶性肿瘤(包括前列腺癌)的临床分级/分期、治疗反应和生存结果之间的关系。因此,在本综述中,我们提供了BMI1作为前列腺癌治疗靶点的潜力的重要证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting Stem Cell Protein BMI1; A Potential Therapeutic Approach forProstate Cancer Therapy
Prostate cancer (CaP) is considered as a vexing challenge for clinical management because of its resistance to the conventional therapies, resulting in most deaths from this disease. The current treatment options including castration shows minimal effect, as most of the patients develop resistance and relapse of more aggressive Castration Resistant Prostate Cancer (CRPC). BMI1 (B cell-specific Moloney murine leukemia virus integration site 1), an oncogenic member of the polycomb group gene family and a transcriptional repressor has emerged as a key regulator in numerous processes including proliferation, differentiation, senescence, and stem cell renewal. Accumulating evidences have also revealed a relationship between BMI1 expression and the clinical grade/stage, therapy response, and survival outcome in most human malignancies, including Prostate cancer. Therefore, in this review, we provide the significant evidences suggesting the potential of BMI1 as a therapeutic target in the management of prostate cancer.
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