Department of Clinical Pharmacy, Akhtar Saeed College of Pharmaceutical Sciences, Bahria Town, Lahore, Pakistan.
Department Clinical Oncology Pharmacy, Cancer Care Hospital & Research Centre, Lahore, Pakistan.
Med Oncol. 2024 Apr 9;41(5):112. doi: 10.1007/s12032-024-02347-z.
Despite recent advancements in the diagnosis and treatment of breast cancer (BC), patient outcomes in terms of survival, recurrence, and disease progression remain suboptimal. A significant factor contributing to these challenges is the cellular heterogeneity within BC, particularly the presence of breast cancer stem cells (BCSCs). These cells are thought to serve as the clonogenic nexus for new tumor growth, owing to their hierarchical organization within the tumor. This descriptive review focuses on the evolving strategies to target BCSCs, which have become a pivotal aspect of therapeutic development. We explore a variety of approaches, including targeting specific tumor surface markers (CD133 and CD44), transporters, heat shock proteins, and critical signaling pathways like Notch, Akt, Hedgehog, KLF4, and Wnt/β-catenin. Additionally, we discuss the modulation of the tumor microenvironment through the CXCR-12/CXCR4 axis, manipulation of pH levels, and targeting hypoxia-inducible factors, vascular endothelial growth factor, and CXCR1/2 receptors. Further, this review focuses on the roles of microRNA expression, strategies to induce apoptosis and differentiation in BCSCs, dietary interventions, dendritic cell vaccination, oncolytic viruses, nanotechnology, immunotherapy, and gene therapy. We particularly focused on studies reporting identification of BCSCs, their unique properties and the efficacy of various therapeutic modalities in targeting these cells. By dissecting these approaches, we aim to provide insights into the complex landscape of BC treatment and the potential pathways for improving patient outcomes through targeted BCSC therapies.
尽管在乳腺癌 (BC) 的诊断和治疗方面取得了最新进展,但在生存、复发和疾病进展方面,患者的结局仍不理想。导致这些挑战的一个重要因素是 BC 中的细胞异质性,特别是乳腺癌干细胞 (BCSCs) 的存在。这些细胞被认为是新肿瘤生长的克隆起源,这归因于它们在肿瘤中的层次组织。本综述重点介绍了针对 BCSCs 的不断发展的策略,这些策略已成为治疗开发的关键方面。我们探讨了各种方法,包括针对特定的肿瘤表面标志物(CD133 和 CD44)、转运蛋白、热休克蛋白以及关键信号通路,如 Notch、Akt、Hedgehog、KLF4 和 Wnt/β-catenin。此外,我们还讨论了通过 CXCR-12/CXCR4 轴调节肿瘤微环境、调节 pH 值以及靶向缺氧诱导因子、血管内皮生长因子和 CXCR1/2 受体。此外,本综述还重点介绍了 microRNA 表达的作用、诱导 BCSC 凋亡和分化的策略、饮食干预、树突状细胞疫苗接种、溶瘤病毒、纳米技术、免疫疗法和基因疗法。我们特别关注了报告鉴定 BCSC、其独特特性以及各种治疗方法靶向这些细胞的疗效的研究。通过剖析这些方法,我们旨在深入了解 BC 治疗的复杂格局以及通过靶向 BCSC 治疗改善患者结局的潜在途径。