IMP-1 inhibits renal cell carcinoma 786-O cell growth by targeting EphrinB2 signaling pathway

IF 0.6 4区 医学 Q4 PHARMACOLOGY & PHARMACY Brazilian Journal of Pharmaceutical Sciences Pub Date : 2023-06-05 DOI:10.1590/s2175-97902023e22102
Juan Liu, Hong Shi
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Abstract

EphrinB2 plays a critical role in tumor growth. In this study, we studied the antitumor activity of imperatorin derivative IMP-1 in renal cell carcinoma (RCC) by regulating EphrinB2 pathway.. Results showed that IMP-1 inhibited the proliferation of 786-O cells in a dose-and time-dependent manner. More importantly, knockdown and transfection of EphrinB2 altered the inhibitory effect of IMP-1 on the activity of 786-O cells. IMP-1 arrested 786-O cell cycle at G0/G1 phase by decreasing the expression of cyclin D1 and cyclin E. Moreover, IMP-1 regulated Bcl-2 family proteins’ expression, thus inducing apoptosis of 786-O cells. IMP-1 down-regulated the expression of EphrinB2, Syntenin1 and PICK1. Then, IMP-1 decreased the phosphorylation of Erk1/2 and AKT. In all, IMP-1 could regulate the EphrinB2 pathway in order to inhibit 786-O cell growth by arresting the cell cycle at G0/G1 phase and inducing cell apoptosis. Thus, IMP-1 may present as a potential strategy for RCC treatment.
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IMP-1靶向EphrinB2信号通路抑制肾细胞癌786-O细胞生长
EphrinB2在肿瘤生长中起关键作用。本研究研究了欧前胡素衍生物IMP-1通过调控EphrinB2通路在肾细胞癌(RCC)中的抗肿瘤活性。结果表明,IMP-1抑制786-O细胞的增殖呈剂量和时间依赖性。更重要的是,敲低和转染EphrinB2改变了IMP-1对786-O细胞活性的抑制作用。IMP-1通过降低cyclin D1和cyclin e的表达,将786-O细胞周期阻滞在G0/G1期,并调控Bcl-2家族蛋白的表达,从而诱导786-O细胞凋亡。IMP-1下调EphrinB2、Syntenin1和PICK1的表达。然后,IMP-1降低Erk1/2和AKT的磷酸化。综上所述,IMP-1可以通过阻滞细胞周期于G0/G1期,诱导细胞凋亡,调控EphrinB2通路,从而抑制786-O细胞的生长。因此,IMP-1可能是RCC治疗的潜在策略。
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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
165
审稿时长
7.5 months
期刊介绍: The Brazilian Journal of Pharmaceutical Sciences accepts for publication Original Papers applicable to the fields of Pharmaceutical Sciences; Reviews and Current Comment Articles, which are published under the Scientific Editor and Associate Editors invitation to recognized experts or when they are spontaneously submitted by the authors in the form of abstracts to have their importance evaluated. A critical view of the subject with insertions of results of previous works in the field in relation to the state of art must be included; Short Communications reporting new methods and previews of works on researches of outstanding importance in which originality justify a quick publication. A maximum of 2000 words excluding tables, figures and references is an acceptable limit. One table, one figure and ten references may be added, and Book Reviews of the latest editions of books, prepared by specialists invited by the Scientific Editor and Associate Editors. Thematic Supplements as well as those related to scientific meetings can be published under the Scientific Editor and/or Associate Editors agreement.
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