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绵羊脐带间充质干细胞对黑色素瘤细胞的抗肿瘤作用

Anti-Tumor Effects of Sheep Umbilical Cord Mesenchymal Stem Cells on Melanoma Cells.

作者信息

Yue Fengjiao, Zhao Yuqing, Lv Yiting, Li Songmei, Wang Weihai, Li Yajun, Wang Shujie, Wang Chunsheng

机构信息

College of Life Science, Northeast Forestry University, Harbin 150040, China.

State Key Laboratory for Animal Disease Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150001, China.

出版信息

Int J Mol Sci. 2025 Jan 6;26(1):426. doi: 10.3390/ijms26010426.

Abstract

Melanoma is among the most common malignancies and has recently exhibited increased resistance to treatments, resulting in a more aggressive disease course. Mesenchymal stem cells (MSCs) secrete cytokines both in vivo and in vitro, which regulate tumor cell signaling pathways and the tumor microenvironment, thereby influencing tumor progression. This study investigates the anti-melanogenesis effects of sheep umbilical cord mesenchymal stem cells (SUCMSCs) to assess their potential application in melanoma treatment. Our findings indicate that, in vitro, SUCMSCs reduce melanin content and tyrosinase activity, inhibit melanoma cell viability, proliferation, migration, and invasion, and promote melanoma cell apoptosis. Subsequent in vivo experiments confirmed that SUCMSCs effectively suppress tumor growth, and histological analysis via HE staining revealed notable differences. Additionally, transcriptome sequencing analysis indicated that the anti-tumor effects were primarily mediated through autophagy, apoptosis, and the TGF-β and NF-κB signaling pathways. The RT-qPCR validation results aligned with the transcriptome data. In summary, SUCMSCs exert anti-melanogenesis effects through the interaction of multiple signaling pathways and cytokines, demonstrating significant potential for melanoma treatment.

摘要

黑色素瘤是最常见的恶性肿瘤之一,最近对治疗的耐药性有所增加,导致病程更具侵袭性。间充质干细胞(MSCs)在体内和体外均分泌细胞因子,这些细胞因子调节肿瘤细胞信号通路和肿瘤微环境,从而影响肿瘤进展。本研究调查了绵羊脐带间充质干细胞(SUCMSCs)的抗黑色素生成作用,以评估其在黑色素瘤治疗中的潜在应用。我们的研究结果表明,在体外,SUCMSCs可降低黑色素含量和酪氨酸酶活性,抑制黑色素瘤细胞的活力、增殖、迁移和侵袭,并促进黑色素瘤细胞凋亡。随后的体内实验证实,SUCMSCs可有效抑制肿瘤生长,HE染色的组织学分析显示出显著差异。此外,转录组测序分析表明,抗肿瘤作用主要通过自噬、凋亡以及TGF-β和NF-κB信号通路介导。RT-qPCR验证结果与转录组数据一致。总之,SUCMSCs通过多种信号通路和细胞因子的相互作用发挥抗黑色素生成作用,显示出在黑色素瘤治疗中的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11720557/f1866a859d2b/ijms-26-00426-g001.jpg

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