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通过紫铆因靶向Mortalin可导致人乳腺癌细胞中肿瘤抑制因子p53激活及转移信号失活。

Targeting Mortalin by Embelin Causes Activation of Tumor Suppressor p53 and Deactivation of Metastatic Signaling in Human Breast Cancer Cells.

作者信息

Nigam Nupur, Grover Abhinav, Goyal Sukriti, Katiyar Shashank P, Bhargava Priyanshu, Wang Pi-Chao, Sundar Durai, Kaul Sunil C, Wadhwa Renu

机构信息

Drug Discovery and Assets Innovation Lab, DBT-AIST International Laboratory for Advanced Biomedicine (DAILAB), Biomedical Research Institute, National Institute of Advanced Industrial Science & Technology (AIST), Tsukuba, Japan; Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Japan.

School of Biotechnology, Jawaharlal Nehru University, New Delhi, India.

出版信息

PLoS One. 2015 Sep 16;10(9):e0138192. doi: 10.1371/journal.pone.0138192. eCollection 2015.

Abstract

Embelin, a natural quinone found in the fruits of Embelia ribes, is commonly used in Ayurvedic home medicine for a variety of therapeutic potentials including anti-inflammation, anti-fever, anti-bacteria and anti-cancer. Molecular mechanisms of these activities and cellular targets have not been clarified to-date. We demonstrate that the embelin inhibits mortalin-p53 interactions, and activates p53 protein in tumor cells. We provide bioinformatics, molecular docking and experimental evidence to the binding affinity of embelin with mortalin and p53. Binding of embelin with mortalin/p53 abrogates their complex resulted in nuclear translocation and transcriptional activation function of p53 causing growth arrest in cancer cells. Furthermore, analyses of growth factors and metastatic signaling using antibody membrane array revealed their downregulation in embelin-treated cells. We also found that the embelin causes transcriptional attenuation of mortalin and several other proteins involved in metastatic signaling in cancer cells. Based on these molecular dynamics and experimental data, it is concluded that the anticancer activity of embelin involves targeting of mortalin, activation of p53 and inactivation of metastatic signaling.

摘要

紫铆因是一种存在于紫铆果实中的天然醌类化合物,在阿育吠陀家庭医学中常用于多种治疗潜力,包括抗炎、退热、抗菌和抗癌。迄今为止,这些活性的分子机制和细胞靶点尚未阐明。我们证明紫铆因抑制mortalin与p53的相互作用,并在肿瘤细胞中激活p53蛋白。我们提供了生物信息学、分子对接和实验证据来证明紫铆因与mortalin和p53的结合亲和力。紫铆因与mortalin/p53的结合消除了它们的复合物,导致p53的核转位和转录激活功能,从而使癌细胞生长停滞。此外,使用抗体膜阵列对生长因子和转移信号进行分析,结果显示在紫铆因处理的细胞中它们被下调。我们还发现紫铆因会导致癌细胞中mortalin和其他几种参与转移信号的蛋白质的转录衰减。基于这些分子动力学和实验数据,得出结论:紫铆因的抗癌活性涉及靶向mortalin、激活p53和使转移信号失活。

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