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Investigational serine/threonine kinase inhibitors against prostate cancer metastases

机译:调查丝氨酸/苏氨酸激酶抑制剂对前列腺癌转移

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摘要

Introduction: Androgen deprivation therapy (ADT) is used as first therapeutic approach in prostate cancer (PCa) although castration resistant disease (CRPC) develops with high frequency. CRPC is the consequence of lack of apoptotic responses to ADT. Alternative targeting of the androgen axis with abiraterone and enzalutamide, as well as taxane-based chemotherapy were used in CRPC. Serine/threonine protein kinases (STKs) regulate different molecular pathways of normal and neoplastic cells and participate to development of CRPC as well as to the progression towards a bone metastatic disease (mCRPC).
机译:介绍:雄激素剥夺治疗(ADT)用作前列腺癌(PCA)的第一治疗方法,尽管抗阉割疾病(CRPC)以高频率发育。 CRPC是对ADT缺乏凋亡反应的结果。 在CRPC中使用雄激素轴和苯甲胺酰胺的雄激素轴的替代靶向,以及基于紫杉烷的化学疗法。 丝氨酸/苏氨酸蛋白激酶(STK)调节正常和肿瘤细胞的不同分子途径,并参与CRPC的开发以及骨转移性疾病的进展(MCRPC)。

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