Abstract

Simple SummaryBreast cancer stem cells are blamed to be responsible for breast cancer tumorigenesis, metastasis, drug resistance and tumor recurrence. Therefore, it is critical to identify this subset of cells and understand their molecular mechanisms for the development of breast cancer treatment strategies. Here, we review the recent advances in breast cancer stem cell studies in terms of available biomarkers, identification and isolation methods, molecular mechanisms, and methods for studying their cellular origin and lineage development.Despite recent advances in diagnosis and treatment, breast cancer (BC) is still a major cause of cancer-related mortality in women. Breast cancer stem cells (BCSCs) are a small but significant subpopulation of heterogeneous breast cancer cells demonstrating strong self-renewal and proliferation properties. Accumulating evidence has proved that BCSCs are the driving force behind BC tumor initiation, progression, metastasis, drug resistance, and recurrence. As a heterogeneous disease, BC contains a full spectrum of different BC subtypes, and different subtypes of BC further exhibit distinct subtypes and proportions of BCSCs, which correspond to different treatment responses and disease-specific outcomes. This review summarized the current knowledge of BCSC biomarkers and their clinical relevance, the methods for the identification and isolation of BCSCs, and the mechanisms regulating BCSCs. We also discussed the cellular origin of BCSCs and the current advances in single-cell lineage tracing and transcriptomics and their potential in identifying the origin and lineage development of BCSCs.

Highlights

  • Breast cancer (BC) is one of the most common leading causes of cancer-related death in women worldwide [1]

  • Increasing evidence has proved the existence of Breast cancer stem cells (BCSCs) and their function during tumor initiation, progression, metastasis, drug resistance, and tumor recurrence

  • The study of BCSCs has significantly advanced our knowledge in the identification, isolation, and characterization of this specific cell population

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Summary

Introduction

Breast cancer (BC) is one of the most common leading causes of cancer-related death in women worldwide [1]. BC is considered a heterogeneous disease with a spectrum of many different subtypes and stages that lead to different treatment responses and disease-specific outcomes [3,4]. Different subtypes of BC can be identified primarily with immunohistochemistry (IHC) [5] and gene expression profiling [6]. According to the IHC/fluorescence in situ hybridization (FISH) profile, BC can be classified and divided on the basis of presence of the estrogen receptor (ER), the progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) into ER-positive, HER2-positive, and triple-negative BC (TNBC) that is defined by the absence of ER, PR, and HER2 [4].

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