STK214947, a novel indole alkaloids, inhibits HeLa and SK-HEP-1 cells survival and EMT process by blocking the Notch3 and Akt signals.

IF 1.8 4区 医学 Q3 ONCOLOGY Anti-Cancer Drugs Pub Date : 2024-04-01 Epub Date: 2024-01-23 DOI:10.1097/CAD.0000000000001568
Zihan Xu, Yuxin Yuan, Jiaqi Liu, Caijing Li, Kejin Chen, Fang Wang, Ganpeng Li
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Abstract

Apoptosis and epithelial-to-mesenchymal transition (EMT) are closely associated with tumor survival and metastasis. These are the basic events in tumor occurrence and progression. STK214947 is an indole alkaloid with a skeleton that is similar to that of indirubin. Indole alkaloids have attracted considerable attention because of their antitumor activity. However, the relationship between STK214947 and these basic events remains unknown. In this study, the effects of STK214947 on inducing apoptosis and reversing the EMT process in tumor cells were confirmed. Mild concentrations of STK214947 inhibited tumor cell migration by reversing EMT and significantly regulated the expression of EMT-related proteins, including Notch3, E-cadherin, N-cadherin and vimentin. In addition, STK214947 in high concentration could induce apoptosis by down-regulating Notch3, p-Akt/Akt, and NF-κB, and upregulating Caspase 3. These findings support the further development of STK214947 as a potential antitumor small molecule that targets Notch3 and Akt signal transduction in cancer.

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STK214947是一种新型吲哚生物碱,它通过抑制Notch3和Akt信号抑制HeLa和SK-HEP-1细胞的存活和EMT过程。
细胞凋亡和上皮细胞向间质转化(EMT)与肿瘤的存活和转移密切相关。这些是肿瘤发生和发展的基本事件。STK214947 是一种吲哚生物碱,其骨架与靛玉红相似。吲哚生物碱因其抗肿瘤活性而备受关注。然而,STK214947 与这些基本事件之间的关系仍然未知。本研究证实了 STK214947 诱导肿瘤细胞凋亡和逆转 EMT 过程的作用。轻度浓度的 STK214947 可通过逆转 EMT 抑制肿瘤细胞的迁移,并显著调控 EMT 相关蛋白的表达,包括 Notch3、E-cadherin、N-cadherin 和波形蛋白。此外,高浓度 STK214947 还能通过下调 Notch3、p-Akt/Akt 和 NF-κB 以及上调 Caspase 3 来诱导细胞凋亡。这些研究结果支持进一步开发 STK214947,将其作为一种针对癌症中 Notch3 和 Akt 信号转导的潜在抗肿瘤小分子。
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来源期刊
Anti-Cancer Drugs
Anti-Cancer Drugs 医学-药学
CiteScore
3.80
自引率
0.00%
发文量
244
审稿时长
3 months
期刊介绍: Anti-Cancer Drugs reports both clinical and experimental results related to anti-cancer drugs, and welcomes contributions on anti-cancer drug design, drug delivery, pharmacology, hormonal and biological modalities and chemotherapy evaluation. An internationally refereed journal devoted to the fast publication of innovative investigations on therapeutic agents against cancer, Anti-Cancer Drugs aims to stimulate and report research on both toxic and non-toxic anti-cancer agents. Consequently, the scope on the journal will cover both conventional cytotoxic chemotherapy and hormonal or biological response modalities such as interleukins and immunotherapy. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors without further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool.
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