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二氢辣椒素通过下调β-连环蛋白信号通路抑制黑色素瘤细胞增殖和转移。

Dihydrocapsaicin Inhibits Cell Proliferation and Metastasis in Melanoma Down-regulating β-Catenin Pathway.

作者信息

Shi Shaomin, Li Chongyang, Zhang Yanli, Deng Chaowei, Liu Wei, Du Juan, Li Qian, Ji Yacong, Guo Leiyang, Liu Lichao, Hu Huanrong, Liu Yaling, Cui Hongjuan

机构信息

Department of Dermatology, Third Hospital of Hebei Medical University, Shijiazhuang, China.

State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.

出版信息

Front Oncol. 2021 Mar 23;11:648052. doi: 10.3389/fonc.2021.648052. eCollection 2021.

Abstract

Dihydrocapsaicin (DHC) is one of the main components of capsaicinoids in Capsicum. It has been reported that DHC exerts anti-cancer effects on diverse malignant tumors, such as colorectal cancer, breast cancer, and glioma. However, studies focused on the effect of DHC upon melanoma have rarely been done. In the present study, melanoma A375 and MV3 cell lines were treated with DHC and the cell proliferation, migration, and invasion were significantly suppressed. Furthermore, DHC effectively inhibited xenograft tumor growth and pulmonary metastasis of melanoma cells in NOD/SCID mice model. It was identified that β-catenin, which plays significant roles in cell proliferation and epithelial-mesenchymal transition, was down-regulated after DHC treatment. In addition, cyclin D1, c-Myc, MMP2, and MMP7, which are critical in diverse cellular process regulation as downstream proteins of β-catenin, were all decreased. Mechanistically, DHC accelerates ubiquitination of β-catenin and up-regulates the beta-transducin repeat containing E3 ubiquitin protein ligase (BTRC) in melanoma cells. The DHC induced suppression of cell proliferation, migration, and invasion were partly rescued by exogenous β-catenin overexpression, both and . Taken together, DHC may serve as a candidate natural compound for human melanoma treatment through β-catenin pathway.

摘要

二氢辣椒素(DHC)是辣椒中辣椒素类物质的主要成分之一。据报道,DHC对多种恶性肿瘤具有抗癌作用,如结直肠癌、乳腺癌和神经胶质瘤。然而,针对DHC对黑色素瘤作用的研究却很少。在本研究中,用DHC处理黑色素瘤A375和MV3细胞系,细胞增殖、迁移和侵袭均受到显著抑制。此外,DHC有效抑制了NOD/SCID小鼠模型中黑色素瘤细胞的异种移植肿瘤生长和肺转移。研究发现,在细胞增殖和上皮-间质转化中起重要作用的β-连环蛋白在DHC处理后表达下调。此外,作为β-连环蛋白下游蛋白,在多种细胞过程调节中起关键作用的细胞周期蛋白D1、c-Myc、基质金属蛋白酶2(MMP2)和基质金属蛋白酶7(MMP7)均减少。机制上,DHC加速黑色素瘤细胞中β-连环蛋白的泛素化,并上调含β-转导素重复序列的E3泛素蛋白连接酶(BTRC)。外源性β-连环蛋白过表达部分挽救了DHC诱导的细胞增殖、迁移和侵袭抑制。综上所述,DHC可能通过β-连环蛋白途径成为治疗人类黑色素瘤的候选天然化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2498/8023049/3a42834b8cee/fonc-11-648052-g001.jpg

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