Effect of gedunin on cell proliferation and apoptosis in skin melanoma cells A431 via the PI3K/JNK signaling pathway.

IF 2.1 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Advances in Clinical and Experimental Medicine Pub Date : 2024-11-12 DOI:10.17219/acem/189729
Wenming Xiao, Zhujing Li, Shiqing Li, Zhiyang Xia, Jianwu Zhang, Hongyan Liu, Wei Chen
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Abstract

Background: Melanoma is an aggressive skin malignancy with rapid metastasis and high morbidity. Gedunin (GN) is a tetranortriterpenoid belonging to the Meliaceae family, described for its anticancer, antiproliferative and apoptotic properties.

Objectives: In the present study, we investigated the effect of GN on A431 melanoma cell proliferation and apoptosis. The inflammatory proteins (tumor necrosis factor alpha (TNF-α), nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), cycloxygenase 2 (COX-2), inducible nitric oxide synthase (iNOS), and interleukin 6 (IL-6)) apoptosis-related proteins, such as Bax, Bcl-2 and caspase-3, and alterations in the PI3K/JNK and p38 pathways in A431 cells after GN treatment were examined.

Material and methods: The cytotoxicity assay and cell apoptosis of GN activity on A431 cells were assessed using MTT assay, acridine orange/ethidium bromide (AO/EB), DAPI (4',6-diamidino-2-phenylindole), propidium iodide (PI), enzyme-linked immunosorbent assay (ELISA), reverse transcription polymerase chain reaction (RT-PCR) and western blot analyses.

Results: The findings demonstrated that GN (10 and 15 μM/mL) inhibits the growth of melanoma cells, triggers apoptosis by enhancing Bax and caspase, and reduces Bcl-2, cyclin-D1, c-myc, and survivin in a concentration-reliant manner. Additionally, GN attenuated the protein expression of inflammatory proteins (TNF-α, NF-κB, COX-2, iNOS, and IL-6) and the cell proliferative PI3K/JNK/p38 signaling pathway. Due to the imbalance in the Bax/Bcl-2 ratio, apoptosis is promoted, and the caspase cascade and Cyt-c are activated. This led us to conclude that GN treatment inhibited Bcl-2, cyclin-D1, c-myc, and survivin activity through the TNF-α/NF-κB and PI3K/JNK/p38 signaling pathways, further preventing the proliferation and stimulation of apoptosis, which contributes to growth arrest in melanoma cells.

Conclusions: Gedunin has been shown to promote melanoma cell death in vitro, suggesting that it could be used as a future treatment for malignant melanoma. Our findings suggested that GN might be applied as a preventative measure in the management of skin melanoma cells.

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格杜宁通过 PI3K/JNK 信号通路对皮肤黑色素瘤细胞 A431 的细胞增殖和凋亡产生影响。
背景:黑色素瘤是一种侵袭性皮肤恶性肿瘤,转移迅速,发病率高。Gedunin (GN) 是一种属于 Meliaceae 家族的四萜类化合物,具有抗癌、抗增殖和细胞凋亡的特性:本研究探讨了 GN 对 A431 黑色素瘤细胞增殖和凋亡的影响。目的:本研究探讨了 GN 对 A431 黑色素瘤细胞增殖和凋亡的影响,并检测了 GN 处理后 A431 细胞中的炎症蛋白(肿瘤坏死因子α(TNF-α)、活化 B 细胞核因子卡巴轻链增强因子(NF-κB)、环氧化酶 2(COX-2)、诱导型一氧化氮合酶(iNOS)和白细胞介素 6(IL-6))、凋亡相关蛋白(如 Bax、Bcl-2 和 caspase-3)以及 PI3K/JNK 和 p38 通路的改变。材料与方法采用 MTT 试验、吖啶橙/溴化乙锭(AO/EB)、DAPI(4',6-二脒基-2-苯基吲哚)、碘化丙啶(PI)、酶联免疫吸附试验(ELISA)、逆转录聚合酶链反应(RT-PCR)和 Western 印迹分析等方法评估 GN 活性对 A431 细胞的细胞毒性和细胞凋亡:研究结果表明,GN(10 和 15 μM/mL)能抑制黑色素瘤细胞的生长,通过增强 Bax 和 caspase 触发细胞凋亡,并以浓度依赖的方式减少 Bcl-2、细胞周期蛋白-D1、c-myc 和存活素。此外,GN 还可减轻炎症蛋白(TNF-α、NF-κB、COX-2、iNOS 和 IL-6)的表达以及细胞增殖的 PI3K/JNK/p38 信号通路。由于 Bax/Bcl-2 的比例失调,细胞凋亡被促进,caspase cascade 和 Cyt-c 被激活。由此我们得出结论:GN治疗可通过TNF-α/NF-κB和PI3K/JNK/p38信号通路抑制Bcl-2、细胞周期蛋白-D1、c-myc和survivin的活性,进一步阻止增殖和刺激凋亡,从而导致黑色素瘤细胞生长停滞:结论:Gedunin在体外促进黑色素瘤细胞死亡的作用已被证实,这表明它未来可用作治疗恶性黑色素瘤的药物。我们的研究结果表明,GN 可作为一种预防性措施用于治疗皮肤黑色素瘤细胞。
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来源期刊
Advances in Clinical and Experimental Medicine
Advances in Clinical and Experimental Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.70
自引率
4.80%
发文量
153
审稿时长
6-12 weeks
期刊介绍: Advances in Clinical and Experimental Medicine has been published by the Wroclaw Medical University since 1992. Establishing the medical journal was the idea of Prof. Bogumił Halawa, Chair of the Department of Cardiology, and was fully supported by the Rector of Wroclaw Medical University, Prof. Zbigniew Knapik. Prof. Halawa was also the first editor-in-chief, between 1992-1997. The journal, then entitled "Postępy Medycyny Klinicznej i Doświadczalnej", appeared quarterly. Prof. Leszek Paradowski was editor-in-chief from 1997-1999. In 1998 he initiated alterations in the profile and cover design of the journal which were accepted by the Editorial Board. The title was changed to Advances in Clinical and Experimental Medicine. Articles in English were welcomed. A number of outstanding representatives of medical science from Poland and abroad were invited to participate in the newly established International Editorial Staff. Prof. Antonina Harłozińska-Szmyrka was editor-in-chief in years 2000-2005, in years 2006-2007 once again prof. Leszek Paradowski and prof. Maria Podolak-Dawidziak was editor-in-chief in years 2008-2016. Since 2017 the editor-in chief is prof. Maciej Bagłaj. Since July 2005, original papers have been published only in English. Case reports are no longer accepted. The manuscripts are reviewed by two independent reviewers and a statistical reviewer, and English texts are proofread by a native speaker. The journal has been indexed in several databases: Scopus, Ulrich’sTM International Periodicals Directory, Index Copernicus and since 2007 in Thomson Reuters databases: Science Citation Index Expanded i Journal Citation Reports/Science Edition. In 2010 the journal obtained Impact Factor which is now 1.179 pts. Articles published in the journal are worth 15 points among Polish journals according to the Polish Committee for Scientific Research and 169.43 points according to the Index Copernicus. Since November 7, 2012, Advances in Clinical and Experimental Medicine has been indexed and included in National Library of Medicine’s MEDLINE database. English abstracts printed in the journal are included and searchable using PubMed http://www.ncbi.nlm.nih.gov/pubmed.
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