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Single-cell transcriptomics reveals cell type diversity of human prostate.

Authors :
Chen Y
Zhang P
Liao J
Cheng J
Zhang Q
Li T
Zhang H
Jiang Y
Zhang F
Zeng Y
Mo L
Yan H
Liu D
Zhang Q
Zou C
Wei GH
Mo Z
Source :
Journal of genetics and genomics = Yi chuan xue bao [J Genet Genomics] 2022 Nov; Vol. 49 (11), pp. 1002-1015. Date of Electronic Publication: 2022 Apr 06.
Publication Year :
2022

Abstract

Extensive studies have been performed to describe the phenotypic changes occurring during malignant transformation of the prostate. However, the cell types and associated changes that contribute to the development of prostate diseases and cancer remain elusive, largely due to the heterogeneous composition of prostatic tissues. Here, we conduct a comprehensive evaluation of four human prostate tissues by single-cell RNA sequencing (scRNA-seq) to analyze their cellular compositions. We identify 18 clusters of cell types, each with distinct gene expression profiles and unique features; of these, one cluster of epithelial cells (Ep) is found to be associated with immune function. In addition, we characterize a special cluster of fibroblasts and aberrant signaling changes associated with prostate cancer (PCa). Moreover, we provide insights into the epithelial changes that occur during the cellular senescence and aging. These results expand our understanding of the unique functional associations between the diverse prostatic cell types and the contributions of specific cell clusters to the malignant transformation of prostate tissues and PCa development.<br />Competing Interests: Conflict of interest The authors have no competing interests to declare.<br /> (Copyright © 2022 Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, and Genetics Society of China. Published by Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1673-8527
Volume :
49
Issue :
11
Database :
MEDLINE
Journal :
Journal of genetics and genomics = Yi chuan xue bao
Publication Type :
Academic Journal
Accession number :
35395421
Full Text :
https://doi.org/10.1016/j.jgg.2022.03.009