Ramesh Saravanan, Selvakumar Preethi, Ameer Mohamed Yazeer, Lian Sen, Abdullah Alzarooni Abdulqadir Ismail M, Ojha Shreesh, Mishra Anshuman, Tiwari Ashutosh, Kaushik Ajeet, Jung Young Do, Chouaib Salem, Lakshmanan Vinoth-Kumar
Prostate Cancer Biomarker Laboratory, Faculty of Clinical Research, Sri Ramachandra Institute of Higher Education and Research, Chennai, India.
Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
Front Oncol. 2023 Mar 9;13:1059441. doi: 10.3389/fonc.2023.1059441. eCollection 2023.
The development of new therapeutic strategies is on the increase for prostate cancer stem cells, owing to current standardized therapies for prostate cancer, including chemotherapy, androgen deprivation therapy (ADT), radiotherapy, and surgery, often failing because of tumor relapse ability. Ultimately, tumor relapse develops into advanced castration-resistant prostate cancer (CRPC), which becomes an irreversible and systemic disease. Hence, early identification of the intracellular components and molecular networks that promote prostate cancer is crucial for disease management and therapeutic intervention. One of the potential therapeutic methods for aggressive prostate cancer is to target prostate cancer stem cells (PCSCs), which appear to be a primary focal point of cancer metastasis and recurrence and are resistant to standardized therapies. PCSCs have also been documented to play a major role in regulating tumorigenesis, sphere formation, and the metastasis ability of prostate cancer with their stemness features. Therefore, the current review highlights the origin and identification of PCSCs and their role in anti-androgen resistance, as well as stemness-related signaling pathways. In addition, the review focuses on the current advanced therapeutic strategies for targeting PCSCs that are helping to prevent prostate cancer initiation and progression, such as microRNAs (miRNAs), nanotechnology, chemotherapy, immunotherapy, the clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) gene-editing system, and photothermal ablation (PTA) therapy.
由于目前用于前列腺癌的标准化疗法(包括化疗、雄激素剥夺疗法(ADT)、放疗和手术)常常因肿瘤复发能力而失败,针对前列腺癌干细胞的新治疗策略正在不断增加。最终,肿瘤复发发展为晚期去势抵抗性前列腺癌(CRPC),这成为一种不可逆转的全身性疾病。因此,早期识别促进前列腺癌的细胞内成分和分子网络对于疾病管理和治疗干预至关重要。侵袭性前列腺癌的一种潜在治疗方法是靶向前列腺癌干细胞(PCSCs),它们似乎是癌症转移和复发的主要焦点,并且对标准化疗法具有抗性。有文献记载,PCSCs凭借其干性特征在调节前列腺癌的肿瘤发生、球体形成和转移能力方面也发挥着重要作用。因此,本综述重点介绍了PCSCs的起源、鉴定及其在抗雄激素耐药性中的作用,以及与干性相关的信号通路。此外,该综述重点关注当前针对PCSCs的先进治疗策略,这些策略有助于预防前列腺癌的发生和进展,如微小RNA(miRNAs)、纳米技术、化疗、免疫疗法、成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关蛋白9(Cas9)基因编辑系统和光热消融(PTA)疗法。