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冬凌草甲素与紫杉醇通过调节 ADORA2A-EMT 相关信号对三阴性乳腺癌的协同抗肿瘤作用。

Synergistic Anti-Tumor Effect of Toosendanin and Paclitaxel on Triple-Negative Breast Cancer via Regulating ADORA2A-EMT Related Signaling.

机构信息

School of Chinese Medicine, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.

School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

出版信息

Adv Biol (Weinh). 2023 Aug;7(8):e2300062. doi: 10.1002/adbi.202300062. Epub 2023 Jul 4.

Abstract

Triple negative breast cancer (TNBC) is an aggressive cancer with very poor prognosis. Combination therapy has proven to be a promising strategy for enhancing TNBC treatment efficacy. Toosendanin (TSN), a plant-derived triterpenoid, has shown pleiotropic effects against a variety of tumors. Herein, it is evaluated whether TSN can enhance the efficacy of paclitaxel (PTX), a common chemotherapeutic agent, against TNBC. It is found that TSN and PTX synergistically suppress the proliferation of TNBC cell lines such as MDA-MB-231 and BT-549, and the combined treatment also inhibits the colony formation and induces cell apoptosis. Furthermore, this combination shows more marked migratory inhibition when compared to PTX alone. Mechanistic study shows that the ADORA2A pathway in TNBC is down-regulated by the combination treatment via mediating epithelial-to-mesenchymal transition (EMT) process. In addition, the combined treatment of TSN and PTX significantly attenuates the tumor growth when compared to PTX monotherapy in a mouse model bearing 4T1 tumor. The results suggest that combination of TSN and PTX is superior to PTX alone, suggesting that it may be a promising alternative adjuvant chemotherapy strategy for patients with TNBC, especially those with metastatic TNBC.

摘要

三阴性乳腺癌(TNBC)是一种侵袭性强、预后极差的癌症。联合治疗已被证明是提高 TNBC 治疗效果的一种有前途的策略。川楝素(TSN)是一种植物来源的三萜类化合物,对多种肿瘤具有多种作用。本研究旨在评估 TSN 是否可以增强紫杉醇(PTX)等常用化疗药物对 TNBC 的疗效。结果发现,TSN 与 PTX 协同抑制 MDA-MB-231 和 BT-549 等 TNBC 细胞系的增殖,联合治疗还抑制集落形成并诱导细胞凋亡。此外,与单独使用 PTX 相比,这种联合治疗表现出更明显的迁移抑制作用。机制研究表明,联合治疗通过介导上皮间质转化(EMT)过程下调 TNBC 中的 ADORA2A 通路。此外,与单独使用 PTX 相比,TSN 和 PTX 的联合治疗在携带 4T1 肿瘤的小鼠模型中显著抑制肿瘤生长。结果表明,TSN 和 PTX 的联合治疗优于单独使用 PTX,提示其可能是 TNBC 患者,特别是转移性 TNBC 患者有前途的辅助化疗策略。

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