Resolving the immune landscape of human prostate at a single-cell level in health and cancer.
Authors
Loudon, Kevin W
Berry, Brendan
Richoz, Nathan
Jones, Julia
Tan, Xiao
Nguyen, Quan
George, Anne
Hori, Satoshi
Field, Sarah
Lynch, Andy G
Kania, Katarzyna
Coupland, Paul
Babbage, Anne
Grenfell, Richard
Publication Date
2021-12-21Journal Title
Cell Rep
ISSN
2211-1247
Publisher
Elsevier BV
Type
Article
This Version
AM
Metadata
Show full item recordCitation
Tuong, K., Loudon, K. W., Berry, B., Richoz, N., Jones, J., Tan, X., Nguyen, Q., et al. (2021). Resolving the immune landscape of human prostate at a single-cell level in health and cancer.. Cell Rep https://doi.org/10.1016/j.celrep.2021.110132
Abstract
The prostate gland produces prostatic fluid, high in zinc and citrate and essential for the maintenance of spermatozoa. Prostate cancer is a common condition with limited treatment efficacy in castration-resistant metastatic disease, including with immune checkpoint inhibitors. Using single-cell RNA-sequencing to perform an unbiased assessment of the cellular landscape of human prostate, we identify a subset of tumor-enriched androgen receptor-negative luminal epithelial cells with increased expression of cancer-associated genes. We also find a variety of innate and adaptive immune cells in normal prostate that were transcriptionally perturbed in prostate cancer. An exception is a prostate-specific, zinc transporter-expressing macrophage population (MAC-MT) that contributes to tissue zinc accumulation in homeostasis but shows enhanced inflammatory gene expression in tumors, including T cell-recruiting chemokines. Remarkably, enrichment of the MAC-MT signature in cancer biopsies is associated with improved disease-free survival, suggesting beneficial antitumor functions.
Sponsorship
Z.K.T. and M.R.C. are supported by a Medical Research Council Human Cell Atlas Research Grant (MR/S035842/1), K.W.L is supported by a Kidney Research UK Clinical Training Fellowship (TF_013_20171124), N.R. was supported by a Wellcome Fellowship (106809/Z/15/Z), M.R.C. is supported by a Versus Arthritis Cure Challenge Research Grant (21777), and an NIHR Research Professorship (RP-2017-08-ST2-002). AYW is supported by the Cancer Research UK Cambridge Centre (C9685/A25177) and NIHR Cambridge Biomedical Research Centre (BRC-1215-20014). Z.K.T. holds an honorary research fellow appointment with The University of Queensland Diamantina Institute. We are grateful for infrastructure support from the Cambridge NIHR Biomedical Campus and Cancer Research UK Cambridge Centre. The NIHR Cambridge Biomedical Research Centre (BRC) is a partnership between Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge, funded by the National Institute for Health Research (NIHR).
Funder references
Cancer Research UK (C96/A25177)
Arthritis Research UK (21777)
Kidney Research UK (TF_013_20171124)
Medical Research Council (MR/S035842/1)
Wellcome Trust (106809/Z/15/Z)
National Institute for Health Research (NIHRDH-IS-BRC-1215-20014)
Identifiers
External DOI: https://doi.org/10.1016/j.celrep.2021.110132
This record's URL: https://www.repository.cam.ac.uk/handle/1810/331161
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