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Inhibition of Bone Marrow-Mesenchymal Stem Cell-Induced Carbonic Anhydrase IX Potentiates Chemotherapy Efficacy in Triple-Negative Breast Cancer Cells.
Sarnella, Annachiara; Ferrara, Ylenia; Albanese, Sandra; Omodei, Daniela; Cerchia, Laura; De Simone, Giuseppina; Supuran, Claudiu T; Zannetti, Antonella.
Afiliação
  • Sarnella A; Institute of Biostructures and Bioimaging, CNR, 80145 Naples, Italy.
  • Ferrara Y; Institute of Biostructures and Bioimaging, CNR, 80145 Naples, Italy.
  • Albanese S; Institute of Biostructures and Bioimaging, CNR, 80145 Naples, Italy.
  • Omodei D; Institute of Biostructures and Bioimaging, CNR, 80145 Naples, Italy.
  • Cerchia L; Institute of Experimental Endocrinology and Oncology "G. Salvatore", CNR, 80131 Naples, Italy.
  • De Simone G; Institute of Biostructures and Bioimaging, CNR, 80145 Naples, Italy.
  • Supuran CT; Department of Neurofarba, University of Florence, 50019 Florence, Italy.
  • Zannetti A; Institute of Biostructures and Bioimaging, CNR, 80145 Naples, Italy.
Cells ; 12(2)2023 01 12.
Article em En | MEDLINE | ID: mdl-36672233
ABSTRACT
Conventional chemotherapy represents the main systemic treatment used for triple-negative breast cancer (TNBC) patients, although many of them develop drug resistance. The hypoxic TME is the crucial driver in the onset of insensitivity to chemotherapy. In this research, we elucidated the role played by bone marrow-derived mesenchymal stem cells (BM-MSCs) in reducing cisplatin effects in TNBC. BT-549 and MDA-MB-231 cells, grown under hypoxic conditions in the presence of conditioned medium obtained from BM-MSCs (CM-MSCs), showed a strong cisplatin insensitivity and increased expression levels of carbonic anhydrase IX (CA IX). Therefore, we inhibited CM-MSC-induced CA IX by SLC-0111 to potentiate chemotherapy efficacy in TNBC cells. Our results showed that CM-MSCs under hypoxic conditions caused an increase in the ability of TNBC cells to form vascular structures, migrate and invade Matrigel. Cell treatment with cisplatin plus SLC-0111 was able to block these mechanisms, as well as the signaling pathways underlying them, such as p-AKT, p-ERK, CD44, MMP-2, vimentin, ß-catenin, and N-cadherin, more effectively than treatment with single agents. In addition, a significant enhancement of apoptosis assessed by annexin V, caspase-3 expression and activity was also shown. Taken together, our results demonstrated the possibility, through CA IX inhibition, of returning TNBC cells to a more chemosensitive state.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco Mesenquimais / Neoplasias de Mama Triplo Negativas Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco Mesenquimais / Neoplasias de Mama Triplo Negativas Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article