Abstract

<div>Abstract<p>The cell of origin and the development of breast cancer are not fully elucidated in <i>BRCA1</i> mutation carriers, especially for estrogen receptor (ER)–positive breast cancers. Here, we performed single-cell RNA sequencing (RNA-seq) on 82,122 cells isolated from the breast cancer tissues and adjacent or prophylactic normal breast tissues from four <i>BRCA1</i> mutation carriers and three noncarriers. Whole-exome sequencing was performed on breast tumors from the four <i>BRCA1</i> mutation carriers; for validation, bulk RNA-seq was performed on adjacent normal breast tissues from eight additional <i>BRCA1</i> mutation carriers and 14 noncarriers. Correlation analyses suggested that breast cancers in <i>BRCA1</i> mutation carriers might originate from luminal cells. The aberrant luminal progenitor cells with impaired differentiation were significantly increased in normal breast tissues in <i>BRCA1</i> mutation carriers compared with noncarriers. These observations were further validated by the bulk RNA-seq data from additional <i>BRCA1</i> mutation carriers. These data suggest that the cell of origin of basal-like breast tumors (ER<sup>neg</sup>) in <i>BRCA1</i> mutation carriers might be luminal progenitor cells. The expression of <i>TP53</i> and <i>BRCA1</i> was decreased in luminal progenitor cells from normal breast tissue in <i>BRCA1</i> mutation carriers, which might trigger the basal/mesenchymal transition of luminal progenitors and might result in basal-like tumor development. Furthermore, ER<sup>high</sup> luminal tumors might originate from mature luminal cells. Our study provides in-depth evidence regarding the cells of origin of different breast cancer subtypes in <i>BRCA1</i> mutation carriers.</p>Significance:<p>Single-cell RNA-seq data indicate that basal-like breast cancer (ER<sup>neg</sup>) might originate from luminal progenitors, and ER<sup>high</sup> luminal breast cancer might originate from mature luminal cells in <i>BRCA1</i> mutation carriers.</p></div>

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