Department of Cell Biology, New York University Grossman School of Medicine, New York, NY, United States.
Division of Hematology and Oncology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, United States.
Int Rev Cell Mol Biol. 2024;388:162-205. doi: 10.1016/bs.ircmb.2024.03.008. Epub 2024 May 6.
Prostate cancer (PCa) stands as a significant global health concern, ranking among the leading causes of cancer deaths in men. While there are several treatment modalities for localized PCa, metastatic castration-resistant PCa (mCRPC) remains incurable. Despite therapeutic advancements showing promise in mCRPC, their impact on overall survival has been limited. This chapter explores the process by which tumors form, reviews our current understanding of PCa progression to mCRPC, and addresses the challenges of boosting anti-tumor immune responses in these tumors. It specifically discusses how chemotactic signaling affects the tumor microenvironment and its role in immune evasion and cancer progression. The chapter further examines the rationale of directly or indirectly targeting these pathways as adjuvant therapies for mCRPC, highlighting recent pre-clinical and clinical studies currently underway. The discussion emphasizes the potential of targeting specific chemokines and chemokine receptors as combination therapies with mainstream treatments for PCa and mCRPC to maximize long-term survival for this deadly disease.
前列腺癌(PCa)是一个全球性的健康问题,是男性癌症死亡的主要原因之一。虽然有几种治疗局限性 PCa 的方法,但转移性去势抵抗性 PCa(mCRPC)仍然无法治愈。尽管治疗进展在 mCRPC 中显示出了希望,但它们对总生存的影响有限。本章探讨了肿瘤形成的过程,回顾了我们目前对 PCa 进展为 mCRPC 的理解,并讨论了增强这些肿瘤中抗肿瘤免疫反应的挑战。它特别讨论了趋化信号如何影响肿瘤微环境及其在免疫逃逸和癌症进展中的作用。本章进一步研究了直接或间接靶向这些途径作为 mCRPC 辅助治疗的原理,强调了针对特定趋化因子和趋化因子受体作为与 PCa 和 mCRPC 主流治疗相结合的治疗方法的潜力,以最大限度地提高这种致命疾病的长期生存。