Dual effect of vitamin D

Breast cancer Calcitriol Fibroblasts Tumor microenvironment Vitamin D3

Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
15 Feb 2024
Historique:
received: 24 10 2023
accepted: 05 02 2024
medline: 16 2 2024
pubmed: 16 2 2024
entrez: 15 2 2024
Statut: epublish

Résumé

Cancer-associated fibroblasts (CAFs) play an important role in the tumor microenvironment. Despite the well-known in vitro antitumoral effect of vitamin D CAFs were cultured with 1 and 10 nM calcitriol and their phenotype; gene expression, protein expression, and secretion were assessed. Calcitriol-treated CAFs-conditioned media (CM) were used to analyze the effect of CAFs on the migration and protein expression of MCF-7 and MDA-MB-231 cells. Tumor tissues from VD The effects of calcitriol on breast CAFs, both at the gene and protein levels, are complex, reflecting the immunosuppressive or procancer properties of CAFs. The anticancer polarization of CAFs following ex vivo calcitriol treatment may result from decreased CCL2, TNC (gene and protein), MMP9, and MMP-2, while the opposite effect may result from increased PDPN, TIMP1 (gene and protein), and SPP1. Despite these multifaceted effects of calcitriol on molecule expression, CAFs' CMs from nonmetastatic and postmenopausal patients treated ex vivo with calcitriol decreased the migration of MCF-7 cells.

Sections du résumé

BACKGROUND BACKGROUND
Cancer-associated fibroblasts (CAFs) play an important role in the tumor microenvironment. Despite the well-known in vitro antitumoral effect of vitamin D
METHODS METHODS
CAFs were cultured with 1 and 10 nM calcitriol and their phenotype; gene expression, protein expression, and secretion were assessed. Calcitriol-treated CAFs-conditioned media (CM) were used to analyze the effect of CAFs on the migration and protein expression of MCF-7 and MDA-MB-231 cells.
RESULTS RESULTS
Tumor tissues from VD
CONCLUSION CONCLUSIONS
The effects of calcitriol on breast CAFs, both at the gene and protein levels, are complex, reflecting the immunosuppressive or procancer properties of CAFs. The anticancer polarization of CAFs following ex vivo calcitriol treatment may result from decreased CCL2, TNC (gene and protein), MMP9, and MMP-2, while the opposite effect may result from increased PDPN, TIMP1 (gene and protein), and SPP1. Despite these multifaceted effects of calcitriol on molecule expression, CAFs' CMs from nonmetastatic and postmenopausal patients treated ex vivo with calcitriol decreased the migration of MCF-7 cells.

Identifiants

pubmed: 38360633
doi: 10.1186/s12885-024-11961-z
pii: 10.1186/s12885-024-11961-z
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

209

Subventions

Organisme : Polish National Science Center
ID : 2017/27/B/NZ5/01167
Organisme : Polish National Science Center
ID : 2017/27/B/NZ5/01167
Organisme : Polish National Science Center
ID : 2017/27/B/NZ5/01167
Organisme : Polish National Science Center
ID : 2017/27/B/NZ5/01167
Organisme : Polish National Science Center
ID : 2017/27/B/NZ5/01167
Organisme : Polish National Science Center
ID : 2017/27/B/NZ5/01167
Organisme : Polish National Science Center
ID : 2017/27/B/NZ5/01167
Organisme : Polish National Science Center
ID : 2017/27/B/NZ5/01167
Organisme : Polish National Science Center
ID : 2017/27/B/NZ5/01167

Informations de copyright

© 2024. The Author(s).

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Auteurs

Natalia Łabędź (N)

Department of Experimental Oncology, Hirszfeld Institute of Immunology and Experimental Therapy, Weigla 12, 53-114, Wroclaw, Poland. natalia.labedz@hirszfeld.pl.
Łukasiewicz Research Network-PORT Polish Center for Technology Development, Stabłowicka 147, 54-066, Wrocław, Poland. natalia.labedz@hirszfeld.pl.

Artur Anisiewicz (A)

Department of Experimental Oncology, Hirszfeld Institute of Immunology and Experimental Therapy, Weigla 12, 53-114, Wroclaw, Poland.

Martyna Stachowicz-Suhs (M)

Department of Experimental Oncology, Hirszfeld Institute of Immunology and Experimental Therapy, Weigla 12, 53-114, Wroclaw, Poland.

Joanna Banach (J)

Department of Experimental Oncology, Hirszfeld Institute of Immunology and Experimental Therapy, Weigla 12, 53-114, Wroclaw, Poland.

Dagmara Kłopotowska (D)

Department of Experimental Oncology, Hirszfeld Institute of Immunology and Experimental Therapy, Weigla 12, 53-114, Wroclaw, Poland.

Adam Maciejczyk (A)

Department of Oncology, Wroclaw Medical University, Pl. Ludwika Hirszfelda 12, 53-413, Wroclaw, Poland.
Lower Silesian Oncology, Pulmonology and Hematology Center, Pl. Ludwika Hirszfelda 12, 53-413, Wroclaw, Poland.

Patrycja Gazińska (P)

Łukasiewicz Research Network-PORT Polish Center for Technology Development, Stabłowicka 147, 54-066, Wrocław, Poland.
Research Oncology, Division of Cancer Studies, Great Maze Pond, King's College London, London, SE1 3SS, UK.

Aleksandra Piotrowska (A)

Division of Histology and Embryology, Department of Human Morphology and Embryology, Wroclaw Medical University, Ul., Chałubińskiego 6a, 50-368, Wroclaw, Poland.

Piotr Dzięgiel (P)

Division of Histology and Embryology, Department of Human Morphology and Embryology, Wroclaw Medical University, Ul., Chałubińskiego 6a, 50-368, Wroclaw, Poland.

Rafał Matkowski (R)

Department of Oncology, Wroclaw Medical University, Pl. Ludwika Hirszfelda 12, 53-413, Wroclaw, Poland.
Lower Silesian Oncology, Pulmonology and Hematology Center, Pl. Ludwika Hirszfelda 12, 53-413, Wroclaw, Poland.

Joanna Wietrzyk (J)

Department of Experimental Oncology, Hirszfeld Institute of Immunology and Experimental Therapy, Weigla 12, 53-114, Wroclaw, Poland.

Classifications MeSH