Cargando…

Alpha-smooth muscle actin-positive cancer-associated fibroblasts secreting osteopontin promote growth of luminal breast cancer

BACKGROUND: Cancer-associated fibroblasts (CAFs) have been shown to support tumor development in a variety of cancers. Different markers were applied to classify CAFs in order to elucidate their impact on tumor progression. However, the exact mechanism by which CAFs enhance cancer development and me...

Descripción completa

Detalles Bibliográficos
Autores principales: Muchlińska, Anna, Nagel, Anna, Popęda, Marta, Szade, Jolanta, Niemira, Magdalena, Zieliński, Jacek, Skokowski, Jarosław, Bednarz-Knoll, Natalia, Żaczek, Anna J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188043/
https://www.ncbi.nlm.nih.gov/pubmed/35690734
http://dx.doi.org/10.1186/s11658-022-00351-7
_version_ 1784725289976201216
author Muchlińska, Anna
Nagel, Anna
Popęda, Marta
Szade, Jolanta
Niemira, Magdalena
Zieliński, Jacek
Skokowski, Jarosław
Bednarz-Knoll, Natalia
Żaczek, Anna J.
author_facet Muchlińska, Anna
Nagel, Anna
Popęda, Marta
Szade, Jolanta
Niemira, Magdalena
Zieliński, Jacek
Skokowski, Jarosław
Bednarz-Knoll, Natalia
Żaczek, Anna J.
author_sort Muchlińska, Anna
collection PubMed
description BACKGROUND: Cancer-associated fibroblasts (CAFs) have been shown to support tumor development in a variety of cancers. Different markers were applied to classify CAFs in order to elucidate their impact on tumor progression. However, the exact mechanism by which CAFs enhance cancer development and metastasis is yet unknown. METHODS: Alpha-smooth muscle actin (α-SMA) was examined immunohistochemically in intratumoral CAFs of nonmetastatic breast cancers and correlated with clinicopathological data. Four CAF cell lines were isolated from patients with luminal breast cancer (lumBC) and classified according to the presence of α-SMA protein. Conditioned medium (CM) from CAF cultures was used to assess the influence of CAFs on lumBC cell lines: MCF7 and T47D cells using Matrigel 3D culture assay. To identify potential factors accounting for promotion of tumor growth by α-SMA(high) CAFs, nCounter PanCancer Immune Profiling Panel (NanoString) was used. RESULTS: In luminal breast cancer, presence of intratumoral CAFs expressing high level of α-SMA (13% of lumBC group) correlated with poor prognosis (p = 0.019). In in vitro conditions, conditioned medium obtained from primary cultures of α-SMA-positive CAFs isolated from luminal tumors was observed to enhance growth of lumBC cell line colonies in 3D Matrigel, in contrast to CM derived from α-SMA-negative CAFs. Multigene expression analysis indicated that osteopontin (OPN) was overexpressed in α-SMA-positive CAFs in both clinical samples and in vitro models. OPN expression was associated with higher percentage of Ki67-positive cells in clinical material (p = 0.012), while OPN blocking in α-SMA-positive CAF-derived CM attenuated growth of lumBC cell line colonies in 3D Matrigel. CONCLUSIONS: Our findings demonstrate that α-SMA-positive CAFs might enhance tumor growth via secretion of OPN. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s11658-022-00351-7.
format Online
Article
Text
id pubmed-9188043
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-91880432022-06-12 Alpha-smooth muscle actin-positive cancer-associated fibroblasts secreting osteopontin promote growth of luminal breast cancer Muchlińska, Anna Nagel, Anna Popęda, Marta Szade, Jolanta Niemira, Magdalena Zieliński, Jacek Skokowski, Jarosław Bednarz-Knoll, Natalia Żaczek, Anna J. Cell Mol Biol Lett Research Letter BACKGROUND: Cancer-associated fibroblasts (CAFs) have been shown to support tumor development in a variety of cancers. Different markers were applied to classify CAFs in order to elucidate their impact on tumor progression. However, the exact mechanism by which CAFs enhance cancer development and metastasis is yet unknown. METHODS: Alpha-smooth muscle actin (α-SMA) was examined immunohistochemically in intratumoral CAFs of nonmetastatic breast cancers and correlated with clinicopathological data. Four CAF cell lines were isolated from patients with luminal breast cancer (lumBC) and classified according to the presence of α-SMA protein. Conditioned medium (CM) from CAF cultures was used to assess the influence of CAFs on lumBC cell lines: MCF7 and T47D cells using Matrigel 3D culture assay. To identify potential factors accounting for promotion of tumor growth by α-SMA(high) CAFs, nCounter PanCancer Immune Profiling Panel (NanoString) was used. RESULTS: In luminal breast cancer, presence of intratumoral CAFs expressing high level of α-SMA (13% of lumBC group) correlated with poor prognosis (p = 0.019). In in vitro conditions, conditioned medium obtained from primary cultures of α-SMA-positive CAFs isolated from luminal tumors was observed to enhance growth of lumBC cell line colonies in 3D Matrigel, in contrast to CM derived from α-SMA-negative CAFs. Multigene expression analysis indicated that osteopontin (OPN) was overexpressed in α-SMA-positive CAFs in both clinical samples and in vitro models. OPN expression was associated with higher percentage of Ki67-positive cells in clinical material (p = 0.012), while OPN blocking in α-SMA-positive CAF-derived CM attenuated growth of lumBC cell line colonies in 3D Matrigel. CONCLUSIONS: Our findings demonstrate that α-SMA-positive CAFs might enhance tumor growth via secretion of OPN. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s11658-022-00351-7. BioMed Central 2022-06-11 /pmc/articles/PMC9188043/ /pubmed/35690734 http://dx.doi.org/10.1186/s11658-022-00351-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Letter
Muchlińska, Anna
Nagel, Anna
Popęda, Marta
Szade, Jolanta
Niemira, Magdalena
Zieliński, Jacek
Skokowski, Jarosław
Bednarz-Knoll, Natalia
Żaczek, Anna J.
Alpha-smooth muscle actin-positive cancer-associated fibroblasts secreting osteopontin promote growth of luminal breast cancer
title Alpha-smooth muscle actin-positive cancer-associated fibroblasts secreting osteopontin promote growth of luminal breast cancer
title_full Alpha-smooth muscle actin-positive cancer-associated fibroblasts secreting osteopontin promote growth of luminal breast cancer
title_fullStr Alpha-smooth muscle actin-positive cancer-associated fibroblasts secreting osteopontin promote growth of luminal breast cancer
title_full_unstemmed Alpha-smooth muscle actin-positive cancer-associated fibroblasts secreting osteopontin promote growth of luminal breast cancer
title_short Alpha-smooth muscle actin-positive cancer-associated fibroblasts secreting osteopontin promote growth of luminal breast cancer
title_sort alpha-smooth muscle actin-positive cancer-associated fibroblasts secreting osteopontin promote growth of luminal breast cancer
topic Research Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188043/
https://www.ncbi.nlm.nih.gov/pubmed/35690734
http://dx.doi.org/10.1186/s11658-022-00351-7
work_keys_str_mv AT muchlinskaanna alphasmoothmuscleactinpositivecancerassociatedfibroblastssecretingosteopontinpromotegrowthofluminalbreastcancer
AT nagelanna alphasmoothmuscleactinpositivecancerassociatedfibroblastssecretingosteopontinpromotegrowthofluminalbreastcancer
AT popedamarta alphasmoothmuscleactinpositivecancerassociatedfibroblastssecretingosteopontinpromotegrowthofluminalbreastcancer
AT szadejolanta alphasmoothmuscleactinpositivecancerassociatedfibroblastssecretingosteopontinpromotegrowthofluminalbreastcancer
AT niemiramagdalena alphasmoothmuscleactinpositivecancerassociatedfibroblastssecretingosteopontinpromotegrowthofluminalbreastcancer
AT zielinskijacek alphasmoothmuscleactinpositivecancerassociatedfibroblastssecretingosteopontinpromotegrowthofluminalbreastcancer
AT skokowskijarosław alphasmoothmuscleactinpositivecancerassociatedfibroblastssecretingosteopontinpromotegrowthofluminalbreastcancer
AT bednarzknollnatalia alphasmoothmuscleactinpositivecancerassociatedfibroblastssecretingosteopontinpromotegrowthofluminalbreastcancer
AT zaczekannaj alphasmoothmuscleactinpositivecancerassociatedfibroblastssecretingosteopontinpromotegrowthofluminalbreastcancer