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**费用诺内酯和脱氢木香内酯联合治疗通过 c-Myc/p53 和 AKT/14-3-3 通路诱导细胞周期停滞和凋亡抑制乳腺癌。**

Costunolide and dehydrocostuslactone combination treatment inhibit breast cancer by inducing cell cycle arrest and apoptosis through c-Myc/p53 and AKT/14-3-3 pathway.

机构信息

Department of Molecular Oncology, Eastern Hepatobiliary Surgical Hospital &National Center of Liver Cancer, Second Military Medical University, Shanghai 200438, China.

School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China.

出版信息

Sci Rep. 2017 Jan 24;7:41254. doi: 10.1038/srep41254.

Abstract

Our previous studies demonstrated that volatile oil from saussurea lappa root (VOSL), rich in two natural sesquiterpene lactones, costunolide (Cos) and dehydrocostuslactone (Dehy), exerts better anti-breast cancer efficacy and lower side effects than Cos or Dehy alone in vivo, however, their anti-cancer molecular mechanisms were still unknown. In this study, we investigated the underlying mechanisms of Cos and Dehy combination treatment (CD) on breast cancer cells through proteomics technology coupled with Western blot validation. Ingenuity Pathways Analysis (IPA) results based on the differentially expressed proteins revealed that both VOSL and CD affect the 14-3-3-mediated signaling, c-Myc mediated apoptosis signaling and protein kinase A (PKA) signaling. Western blot coupled with cell cycle and apoptosis analysis validated the results of proteomics analysis. Cell cycle arrest and apoptosis were induced in a dose-dependent manner, and the expressions of p53 and p-14-3-3 were significantly up-regulated, whereas the expressions of c-Myc, p-AKT, p-BID were significantly down-regulated, furthermore, the ratio of BAX/BCL-2 were significantly increased in breast cancer cells after CD and VOSL treatment. The findings indicated that VOSL and CD could induce breast cancer cell cycle arrest and apoptosis through c-Myc/p53 and AKT/14-3-3 signaling pathways and may be novel effective candidates for breast cancer treatment.

摘要

我们之前的研究表明,藏药瑞香狼毒根挥发油(VOSL)富含两种天然倍半萜内酯,即木香烃内酯(Cos)和去氢木香内酯(Dehy),在体内比单独使用 Cos 或 Dehy 具有更好的抗乳腺癌疗效和更低的副作用,但它们的抗癌分子机制尚不清楚。在这项研究中,我们通过蛋白质组学技术结合 Western blot 验证,研究了 Cos 和 Dehy 联合治疗(CD)对乳腺癌细胞的潜在机制。基于差异表达蛋白的 IPA 结果表明,VOSL 和 CD 均影响 14-3-3 介导的信号转导、c-Myc 介导的细胞凋亡信号转导和蛋白激酶 A(PKA)信号转导。Western blot 结合细胞周期和凋亡分析验证了蛋白质组学分析的结果。细胞周期阻滞和凋亡呈剂量依赖性诱导,p53 和 p-14-3-3 的表达显著上调,而 c-Myc、p-AKT、p-BID 的表达显著下调,此外,CD 和 VOSL 处理后乳腺癌细胞中 BAX/BCL-2 的比值显著增加。这些发现表明,VOSL 和 CD 可以通过 c-Myc/p53 和 AKT/14-3-3 信号通路诱导乳腺癌细胞周期阻滞和凋亡,可能是治疗乳腺癌的新有效候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/237b/5259746/7cf2190de9b2/srep41254-f1.jpg

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