Wang Lei, Jin Zeng, Master Rohan P, Maharjan Chandra K, Carelock Madison E, Reccoppa Tiffany B A, Kim Myung-Chul, Kolb Ryan, Zhang Weizhou
Department of Pathology, Immunology and Laboratory Medicine, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
Immunology Concentration, Biomedical Graduate Program, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
Cancers (Basel). 2022 Jul 5;14(13):3287. doi: 10.3390/cancers14133287.
Breast cancer stem cells (BCSCs) constitute a small population of cells within breast cancer and are characterized by their ability to self-renew, differentiate, and recapitulate the heterogeneity of the tumor. Clinically, BCSCs have been correlated with cancer progression, metastasis, relapse, and drug resistance. The tumorigenic roles of BCSCs have been extensively reviewed and will not be the major focus of the current review. Here, we aim to highlight how the crucial intrinsic signaling pathways regulate the fate of BCSCs, including the Wnt, Notch, Hedgehog, and NF-κB signaling pathways, as well as how different cell populations crosstalk with BCSCs within the TME, including adipocytes, endothelial cells, fibroblasts, and immune cells. Based on the molecular and cellular activities of BCSCs, we will also summarize the targeting strategies for BCSCs and related clinical trials. This review will highlight that BCSC development in breast cancer is impacted by both BCSC endogenous signaling and external factors in the TME, which provides an insight into how to establish a comprehensively therapeutic strategy to target BCSCs for breast cancer treatments.
乳腺癌干细胞(BCSCs)是乳腺癌中的一小部分细胞,其特征在于具有自我更新、分化以及重现肿瘤异质性的能力。在临床上,BCSCs与癌症进展、转移、复发和耐药性相关。BCSCs的致瘤作用已得到广泛综述,并非本综述的主要重点。在此,我们旨在强调关键的内在信号通路如何调节BCSCs的命运,包括Wnt、Notch、Hedgehog和NF-κB信号通路,以及不同细胞群体如何在肿瘤微环境(TME)中与BCSCs发生相互作用,这些细胞群体包括脂肪细胞、内皮细胞、成纤维细胞和免疫细胞。基于BCSCs的分子和细胞活性,我们还将总结针对BCSCs的靶向策略及相关临床试验。本综述将强调,乳腺癌中BCSCs的发育受到BCSCs内源性信号和TME中外部因素的影响,这为如何建立全面的治疗策略以靶向BCSCs进行乳腺癌治疗提供了见解。