Cargando…
A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer
Outcomes for men with localized prostate cancer vary widely, with some men effectively managed without treatment on active surveillance, while other men rapidly progress to metastatic disease despite curative‐intent therapies. One of the strongest prognostic indicators of outcome is grade groups bas...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073007/ https://www.ncbi.nlm.nih.gov/pubmed/33600062 http://dx.doi.org/10.1002/cjp2.205 |
_version_ | 1783684034379907072 |
---|---|
author | Hesterberg, Amanda B Rios, Brenda L Wolf, Elysa M Tubbs, Colby Wong, Hong Yuen Schaffer, Kerry R Lotan, Tamara L Giannico, Giovanna A Gordetsky, Jennifer B Hurley, Paula J |
author_facet | Hesterberg, Amanda B Rios, Brenda L Wolf, Elysa M Tubbs, Colby Wong, Hong Yuen Schaffer, Kerry R Lotan, Tamara L Giannico, Giovanna A Gordetsky, Jennifer B Hurley, Paula J |
author_sort | Hesterberg, Amanda B |
collection | PubMed |
description | Outcomes for men with localized prostate cancer vary widely, with some men effectively managed without treatment on active surveillance, while other men rapidly progress to metastatic disease despite curative‐intent therapies. One of the strongest prognostic indicators of outcome is grade groups based on the Gleason grading system. Gleason grade 4 prostate cancer with cribriform morphology is associated with adverse outcomes and can be utilized clinically to improve risk stratification. The underpinnings of disease aggressiveness associated with cribriform architecture are not fully understood. Most studies have focused on genetic and molecular alterations in cribriform tumor cells; however, less is known about the tumor microenvironment in cribriform prostate cancer. Cancer‐associated fibroblasts (CAFs) are a heterogeneous population of fibroblasts in the tumor microenvironment that impact cancer aggressiveness. The overall goal of this study was to determine if cribriform prostate cancers are associated with a unique repertoire of CAFs. Radical prostatectomy whole‐tissue sections were analyzed for the expression of fibroblast markers (ASPN in combination with FAP, THY1, ENG, NT5E, TNC, and PDGFRβ) in stroma adjacent to benign glands and in Gleason grade 3, Gleason grade 4 cribriform, and Gleason grade 4 noncribriform prostate cancer by RNAscope®. Halo® Software was used to quantify percent positive stromal cells and expression per positive cell. The fibroblast subtypes enriched in prostate cancer were highly heterogeneous. Both overlapping and distinct populations of low abundant fibroblast subtypes in benign prostate stroma were enriched in Gleason grade 4 prostate cancer with cribriform morphology compared to Gleason grade 4 prostate cancer with noncribriform morphology and Gleason grade 3 prostate cancer. In addition, gene expression was distinctly altered in CAF subtypes adjacent to cribriform prostate cancer. Overall, these studies suggest that cribriform prostate cancer has a unique tumor microenvironment that may distinguish it from other Gleason grade 4 morphologies and lower Gleason grades. |
format | Online Article Text |
id | pubmed-8073007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80730072021-04-29 A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer Hesterberg, Amanda B Rios, Brenda L Wolf, Elysa M Tubbs, Colby Wong, Hong Yuen Schaffer, Kerry R Lotan, Tamara L Giannico, Giovanna A Gordetsky, Jennifer B Hurley, Paula J J Pathol Clin Res Original Articles Outcomes for men with localized prostate cancer vary widely, with some men effectively managed without treatment on active surveillance, while other men rapidly progress to metastatic disease despite curative‐intent therapies. One of the strongest prognostic indicators of outcome is grade groups based on the Gleason grading system. Gleason grade 4 prostate cancer with cribriform morphology is associated with adverse outcomes and can be utilized clinically to improve risk stratification. The underpinnings of disease aggressiveness associated with cribriform architecture are not fully understood. Most studies have focused on genetic and molecular alterations in cribriform tumor cells; however, less is known about the tumor microenvironment in cribriform prostate cancer. Cancer‐associated fibroblasts (CAFs) are a heterogeneous population of fibroblasts in the tumor microenvironment that impact cancer aggressiveness. The overall goal of this study was to determine if cribriform prostate cancers are associated with a unique repertoire of CAFs. Radical prostatectomy whole‐tissue sections were analyzed for the expression of fibroblast markers (ASPN in combination with FAP, THY1, ENG, NT5E, TNC, and PDGFRβ) in stroma adjacent to benign glands and in Gleason grade 3, Gleason grade 4 cribriform, and Gleason grade 4 noncribriform prostate cancer by RNAscope®. Halo® Software was used to quantify percent positive stromal cells and expression per positive cell. The fibroblast subtypes enriched in prostate cancer were highly heterogeneous. Both overlapping and distinct populations of low abundant fibroblast subtypes in benign prostate stroma were enriched in Gleason grade 4 prostate cancer with cribriform morphology compared to Gleason grade 4 prostate cancer with noncribriform morphology and Gleason grade 3 prostate cancer. In addition, gene expression was distinctly altered in CAF subtypes adjacent to cribriform prostate cancer. Overall, these studies suggest that cribriform prostate cancer has a unique tumor microenvironment that may distinguish it from other Gleason grade 4 morphologies and lower Gleason grades. John Wiley & Sons, Inc. 2021-02-18 /pmc/articles/PMC8073007/ /pubmed/33600062 http://dx.doi.org/10.1002/cjp2.205 Text en © 2021 The Authors. The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland & John Wiley & Sons, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Hesterberg, Amanda B Rios, Brenda L Wolf, Elysa M Tubbs, Colby Wong, Hong Yuen Schaffer, Kerry R Lotan, Tamara L Giannico, Giovanna A Gordetsky, Jennifer B Hurley, Paula J A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer |
title | A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer |
title_full | A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer |
title_fullStr | A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer |
title_full_unstemmed | A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer |
title_short | A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer |
title_sort | distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073007/ https://www.ncbi.nlm.nih.gov/pubmed/33600062 http://dx.doi.org/10.1002/cjp2.205 |
work_keys_str_mv | AT hesterbergamandab adistinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT riosbrendal adistinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT wolfelysam adistinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT tubbscolby adistinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT wonghongyuen adistinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT schafferkerryr adistinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT lotantamaral adistinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT giannicogiovannaa adistinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT gordetskyjenniferb adistinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT hurleypaulaj adistinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT hesterbergamandab distinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT riosbrendal distinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT wolfelysam distinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT tubbscolby distinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT wonghongyuen distinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT schafferkerryr distinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT lotantamaral distinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT giannicogiovannaa distinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT gordetskyjenniferb distinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer AT hurleypaulaj distinctrepertoireofcancerassociatedfibroblastsisenrichedincribriformprostatecancer |