Suppr超能文献

大麻环萜内酯,一种新型的倍半萜内酯,通过失活 STAT3 来抑制三阴性乳腺癌的生长、转移和 BCSCS 样特征。

Eucannabinolide, a novel sesquiterpene lactone, suppresses the growth, metastasis and BCSCS-like traits of TNBC via inactivation of STAT3.

机构信息

College of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.

College of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.

出版信息

Neoplasia. 2021 Jan;23(1):36-48. doi: 10.1016/j.neo.2020.10.012. Epub 2020 Nov 18.

Abstract

Signal transducer and activator of transcription 3 (STAT3) is an important therapeutic target to triple negative breast cancer (TNBC) treatment. In the present study, we aim to investigate the potential activity of Eucannabinolide (Euc), a novel sesquiterpene lactone separated from Eupatorium cannabinum Linn. against TNBC by targeting STAT3 and expect that Euc will be developed as an inhibitor of STAT3 in the treatment of TNBC. We found that Euc effectively suppressed STAT3 activation at tyrosine 705, inhibited its translocation to nucleus, and decreased its DNA binding capacity. Moreover, introduction of STAT3-short hairpin RNAs or STAT3 inhibitor S3I-201 attenuates the Euc-induced inhibition of cell viability. And, Euc inhibited cell viability, proliferation, metastasis and breast cancer stem cell-like traits but did not induce cytotoxicity in human mammary epithelial cells. The in vivo study similarly demonstrated that administration of Euc inhibited the growth of xenograft tumors and impaired tumor metastasis of a lung metastasis model. The above phenomena were associated with STAT3 dysfunction induced by Euc. In conclusion, Euc elicits the effects of anti-proliferation, anti-metastasis and anti-breast cancer stem cell-like traits in TNBC via targeting STAT3. These data highlight that development of Euc as a STAT3 inhibitor may offer a promising therapeutic strategy for TNBC.

摘要

信号转导子和转录激活子 3(STAT3)是治疗三阴性乳腺癌(TNBC)的重要治疗靶点。在本研究中,我们旨在通过靶向 STAT3 来研究从大麻泽兰中分离得到的新型倍半萜内酯 Eucannabinolide(Euc)对 TNBC 的潜在活性,并期望 Euc 将被开发为治疗 TNBC 的 STAT3 抑制剂。我们发现 Euc 能有效抑制 STAT3 酪氨酸 705 的激活,抑制其向核内转移,并降低其 DNA 结合能力。此外,STAT3-short hairpin RNA 的引入或 STAT3 抑制剂 S3I-201 减弱了 Euc 诱导的细胞活力抑制作用。而且,Euc 抑制细胞活力、增殖、转移和乳腺癌干细胞样特性,但在人乳腺上皮细胞中不诱导细胞毒性。体内研究同样表明,Euc 的给药抑制了异种移植物肿瘤的生长并损害了肺转移模型中的肿瘤转移。上述现象与 Euc 诱导的 STAT3 功能障碍有关。总之,Euc 通过靶向 STAT3 在 TNBC 中发挥抗增殖、抗转移和抗乳腺癌干细胞样特性的作用。这些数据强调了将 Euc 开发为 STAT3 抑制剂可能为 TNBC 提供一种有前途的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d86f/7683293/312b69d97807/gr1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验