Institute of Biostructures and Bioimaging, CNR, 80145 Naples, Italy.
Institute of Experimental Endocrinology and Oncology "G. Salvatore", CNR, 80131 Naples, Italy.
Cells. 2023 Jan 12;12(2):298. doi: 10.3390/cells12020298.
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, β-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.
传统化疗是三阴性乳腺癌 (TNBC) 患者的主要全身治疗方法,尽管许多患者都会产生耐药性。缺氧的 TME 是导致对化疗不敏感的关键驱动因素。在这项研究中,我们阐明了骨髓间充质干细胞 (BM-MSCs) 在降低 TNBC 中顺铂作用中的作用。在缺氧条件下生长的 BT-549 和 MDA-MB-231 细胞,在 BM-MSCs(CM-MSCs)来源的条件培养基存在下培养,表现出强烈的顺铂耐药性和碳酸酐酶 IX(CA IX)表达水平增加。因此,我们通过 SLC-0111 抑制 CM-MSC 诱导的 CA IX 以增强 TNBC 细胞的化疗疗效。我们的结果表明,在缺氧条件下的 CM-MSCs 导致 TNBC 细胞形成血管结构、迁移和侵袭 Matrigel 的能力增加。用顺铂加 SLC-0111 处理细胞能够阻断这些机制,以及它们的信号通路,如 p-AKT、p-ERK、CD44、MMP-2、波形蛋白、β-连环蛋白和 N-钙黏蛋白,比单独用药更有效。此外,还通过 annexin V、caspase-3 表达和活性评估了明显增强的细胞凋亡。总之,我们的结果表明,通过抑制 CA IX,有可能使 TNBC 细胞恢复到更敏感的化疗状态。