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山豆根宁调节miR-374a/GADD45A轴以抑制三阴性乳腺癌的起始和进展。

Maackiain Modulates miR-374a/GADD45A Axis to Inhibit Triple-Negative Breast Cancer Initiation and Progression.

作者信息

Peng Fu, Wang Li, Xiong Liang, Tang Hailin, Du Junrong, Peng Cheng

机构信息

Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu, China.

State Key Laboratory of Southwestern Chinese Medicine Resources, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Front Pharmacol. 2022 Mar 4;13:806869. doi: 10.3389/fphar.2022.806869. eCollection 2022.

Abstract

Breast cancer ranks as the leading cause of death in lethal malignancies among women worldwide, with a sharp increase of incidence since 2008. Triple negative breast cancer (TNBC) gives rise to the largest proportion in breast cancer-related deaths because of its aggressive growth and rapid metastasis. Hence, searching for promising targets and innovative approaches is indispensable for the TNBC treatment. Maackiain (MA), a natural compound with multiple biological activities, could be isolated from different Chinese herbs, such as and . It was the first time to report the anti-cancer effect of MA in TNBC. MA could suppress TNBC cell proliferation, foci formation, migration, and invasion. MA also exerted a significant inhibitory effect on tumor growth of TNBC. Furthermore, MA could induce apoptosis with an increase of GADD45α and a decrease of miR-374a. In contrast, overexpressing miR-374a would result in at least partly affecting the proapoptotic effect of MA and suppressing GADD45α stimulated by MA. These results reveal the anti-TNBC effect of MA and , providing evidence for its potential as a drug candidate utilized in TNBC therapy.

摘要

乳腺癌是全球女性致命恶性肿瘤中的主要死因,自2008年以来发病率急剧上升。三阴性乳腺癌(TNBC)因其侵袭性生长和快速转移,在乳腺癌相关死亡中占比最大。因此,寻找有前景的靶点和创新方法对于TNBC治疗至关重要。山萘酚(MA)是一种具有多种生物活性的天然化合物,可从不同的中草药中分离得到,如[此处原文缺失具体草药名称]。首次报道了MA在TNBC中的抗癌作用。MA可抑制TNBC细胞增殖、集落形成、迁移和侵袭。MA对TNBC的肿瘤生长也有显著抑制作用。此外,MA可通过增加GADD45α和降低miR-374a诱导细胞凋亡。相反,过表达miR-374a至少会部分影响MA的促凋亡作用,并抑制MA刺激的GADD45α。这些结果揭示了MA的抗TNBC作用,为其作为TNBC治疗候选药物的潜力提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7304/8930825/c2a818e7bfe9/fphar-13-806869-g001.jpg

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