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人子宫颈间充质干细胞分泌组与紫杉醇对三阴性乳腺癌的协同作用

英文原题:Synergistic effect of human uterine cervical mesenchymal stem cell secretome and paclitaxel on triple negative breast cancer.

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Synergistic effect of human uterine cervical mesenchymal stem cell secretome and paclitaxel on triple negative breast cancer.

PubMed 2024/04/25(内容时间) Stem Cell Res Ther Q1 · IF 7.8(JCR 2025)

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研究概要

我们的数据表明,CM-hUCESC 与紫杉醇联合在 TNBC 中具有协同作用,并提供了降低化疗药物剂量的机会,从而可能减轻化疗相关毒性。

中文摘要

三阴性乳腺癌(TNBC)是乳腺癌中致死性最高的亚型。尽管化疗有不良反应,仍是 TNBC 的标准全身治疗。由于联合不同药物以提高疗效和治愈潜力至关重要,间充质干细胞(MSC)分泌组可能是一种创新替代方案。

本研究拟探讨化疗药物紫杉醇与复杂生物制品——人宫颈干细胞分泌组(CM-hUCESC)联合用于 TNBC 的抗肿瘤作用。

紫杉醇与 CM-hUCESC 联合可降低肿瘤细胞增殖和侵袭性,并在体外诱导细胞凋亡(MDA-MB-231 细胞和/或原代肿瘤细胞)。小鼠肿瘤异种移植模型证实了抗肿瘤作用,两种制品联合可显著抑制肿瘤生长。此外,以亚致死剂量紫杉醇对 hUCESC 预处理,可增强其分泌组作用;与紫杉醇联合后进一步显著抑制肿瘤生长,甚至可降低体内紫杉醇剂量。这种效应部分由 CM-hUCESC 来源的细胞外囊泡(EV)及 TIMP-1 和 TIMP-2 等可溶性因子介导。

数据表明 CM-hUCESC 与紫杉醇联合对 TNBC 具有协同作用,并为降低化疗药物剂量提供可能,从而或可减少化疗相关毒性。

展开英文摘要原文

Triple-negative breast cancer (TNBC) is the most lethal subtype of breast cancer and, despite its adverse effects, chemotherapy is the standard systemic treatment option for TNBC. Since, it is of utmost importance to consider the combination of different agents to achieve greater efficacy and curability potential, MSC secretome is a possible innovative alternative.

In the present study, we proposed to investigate the anti-tumor effect of the combination of a chemical agent (paclitaxel) with a complex biological product, secretome derived from human Uterine Cervical Stem cells (CM-hUCESC) in TNBC.

The combination of paclitaxel and CM-hUCESC decreased cell proliferation and invasiveness of tumor cells and induced apoptosis in vitro (MDA-MB-231 and/or primary tumor cells). The anti-tumor effect was confirmed in a mouse tumor xenograft model showing that the combination of both products has a significant effect in reducing tumor growth. Also, pre-conditioning hUCESC with a sub-lethal dose of paclitaxel enhances the effect of its secretome and in combination with paclitaxel reduced significantly tumor growth and even allows to diminish the dose of paclitaxel in vivo. This effect is in part due to the action of extracellular vesicles (EVs) derived from CM-hUCESC and soluble factors, such as TIMP-1 and - 2.

In conclusion, our data demonstrate the synergistic effect of the combination of CM-hUCESC with paclitaxel on TNBC and opens an opportunity to reduce the dose of the chemotherapeutic agents, which may decrease chemotherapy-related toxicity.

论文信息

作者
Eiro N、Fraile M、Escudero-Cernuda S、Sendon-Lago J、Gonzalez LO、Fernandez-Sánchez ML、Vizoso FJ
第一作者单位
Research Unit, Hospital de Jove Foundation, Gijón, Spain. noemi.eiro@hospitaldejove.com.Spain
通讯作者单位
Research Unit, Hospital de Jove Foundation, Gijón, Spain. investigacion@hospitaldejove.com.Spain
文献类型
非美国政府资助研究
期刊
Stem cell research & therapy2024 Apr 25
原文标识
PubMed 38664697 · DOI 10.1186/s13287-024-03717-0