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抑制 STAT3 信号通路参与了由苦参和金银花组成的中药复方的抗黑色素瘤作用。

Inhibiting STAT3 signaling is involved in the anti-melanoma effects of a herbal formula comprising Sophorae Flos and Lonicerae Japonicae Flos.

机构信息

Center for Cancer and Inflammation Research, School of Chinese Medicine, Hong Kong Baptist University, Kowloon Tong, Hong Kong, China.

Research and Development Centre for Natural Health Products, HKBU Shenzhen Research Institute and Continuing Education, Shenzhen, China.

出版信息

Sci Rep. 2017 Jun 8;7(1):3097. doi: 10.1038/s41598-017-03351-2.

Abstract

A herbal formula (SL) comprising Sophorae Flos and Lonicerae Japonicae Flos was traditionally used to treat melanoma. Constitutively active signal transducer and activator of transcription 3 (STAT3) has been proposed as a therapeutic target in melanoma. Here we investigated whether an ethanolic extract of SL (SLE) exerted anti-melanoma activities by inhibiting STAT3 signaling. B16F10 allograft model, A375 and B16F10 cells were employed to assess the in vivo and in vitro anti-melanoma activities of SLE. A375 cells stably expressing STAT3C, a constitutively active STAT3 mutant, were used to determine the role of STAT3 signaling in SLE's anti-melanoma effects. Intragastric administration of SLE (1.2 g/kg) potently inhibited melanoma growth in mice and inhibited STAT3 phosphorylation in the tumors. In cultured cells, SLE dramatically reduced cell viability, induced apoptosis, suppressed migration and invasion, and restrained STAT3 activation and nuclear localization. STAT3C overexpression in A375 cells diminished SLE's effects on cell viability, apoptosis and invasion. Collectively, SLE exerted potent anti-melanoma effects partially by inhibiting STAT3 signaling. This study provides pharmacological justification for the traditional use of this formula in treating melanoma, and suggests that SLE has the potential to be developed as a modern alternative and/or complimentary agent for melanoma treatment and prevention.

摘要

一种包含苦参和金银花的草药配方(SL)传统上用于治疗黑色素瘤。组成性激活的信号转导和转录激活因子 3(STAT3)已被提议作为黑色素瘤的治疗靶点。在这里,我们研究了 SL 的乙醇提取物(SLE)是否通过抑制 STAT3 信号传导发挥抗黑色素瘤活性。B16F10 同种异体移植模型、A375 和 B16F10 细胞被用于评估 SLE 的体内和体外抗黑色素瘤活性。使用稳定表达组成性激活 STAT3 突变体 STAT3C 的 A375 细胞来确定 STAT3 信号在 SLE 的抗黑色素瘤作用中的作用。SLE(1.2 g/kg)的胃内给药强烈抑制了小鼠黑色素瘤的生长,并抑制了肿瘤中的 STAT3 磷酸化。在培养的细胞中,SLE 显著降低细胞活力,诱导细胞凋亡,抑制迁移和侵袭,并抑制 STAT3 激活和核定位。A375 细胞中 STAT3C 的过表达减弱了 SLE 对细胞活力、细胞凋亡和侵袭的影响。总之,SLE 通过抑制 STAT3 信号发挥强大的抗黑色素瘤作用。这项研究为该配方在治疗黑色素瘤中的传统用途提供了药理学依据,并表明 SLE 有可能被开发为治疗和预防黑色素瘤的现代替代药物和/或补充药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/4b1a3bec1802/41598_2017_3351_Fig1_HTML.jpg

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