Literature DB >> 28385077

Proteomic Analysis and Functional Studies of Baicalin on Proteins Associated with Skin Cancer.

Dan Li1, Bingjiang Lin1, Nabiha Yusuf2, Erin M Burns2, Xiuqin Yu3, Dan Luo1, Wei Min3.   

Abstract

Abundant evidence supports the key role of ultraviolet radiation (UVR) in skin cancer development. The human skin, especially the epidermal layer, is the main defense against UV radiation. Baicalin is a major bioactive component of Scutellaria baicalensis Georgi, a plant which has been found to exhibit antitumor activity. The anticarcinogenic mechanism of baicalin is not completely understood. We have reported that baicalin inhibited UVB-induced photo-damage and apoptosis in HaCaT cells (human skin keratinocytes). The aim of the present study is to investigate the cellular gene targets responsible for baicalin's antitumor activity by performing two-dimensional electrophoresis liquid chromatography-mass spectrometry/mass spectrometry (2-DE LC-MS/MS) with HaCaT cells following UVB and baicalin exposure. Two-DE for protein separation was performed, followed by matrix-assisted laser desorption/ionization mass spectrometry and database searches. Nucleophosmin (NPM)-specific siRNA was designed and synthesized, and the small interfering RNA was transfected into skin squamous cancer A431 cells to knockdown the NPM expression. Proliferation and cell cycle status were assessed by CCK8 and flow cytometric analyses, respectively. We have identified 38 protein spots that are differentially expressed in HaCaT cells exposed to baicalin and/or UVB irradiation These proteins are involved in detoxification, proliferation, metabolism, cytoskeleton and motility. In particular, we found several proteins that have been linked to tumor progression and resistance, such as NPMBaicalin treatment reduced the cellular proliferation rate and induced arrest during the S-phase of the cell cycle in A431 cells. NPM1 silencing significantly enhanced the effect of baicalin. Our data indicated that baicalin results in the significant inhibition of tumor growth in the A431 cell line, which may be associated with the regulation of the NPM gene expression.

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Keywords:  Baicalin; Keratinocyte HaCaT cells; NPM; Proteomics; Skin; Squamous Cancer A431 cells; UVB

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Year:  2017        PMID: 28385077     DOI: 10.1142/S0192415X17500355

Source DB:  PubMed          Journal:  Am J Chin Med        ISSN: 0192-415X            Impact factor:   4.667


  3 in total

1.  Differential expression of NPM, GSTA3, and GNMT in mouse liver following long-term in vivo irradiation by means of uranium tailings.

Authors:  Lan Yi; Hongxiang Mu; Nan Hu; Jing Sun; Jie Yin; Keren Dai; Dingxin Long; Dexin Ding
Journal:  Biosci Rep       Date:  2018-10-17       Impact factor: 3.840

2.  Baicalin Regulates Proliferation, Apoptosis, Migration, and Invasion in Mesothelioma.

Authors:  Wen-Fei Xu; Feng Liu; Yi-Cong Ma; Zhi-Rong Qian; Long Shi; Hang Mu; Feng Ding; Xue-Qi Fu; Xu-Hui Li
Journal:  Med Sci Monit       Date:  2019-10-31

3.  Induction of Autophagy by Baicalin Through the AMPK-mTOR Pathway Protects Human Skin Fibroblasts from Ultraviolet B Radiation-Induced Apoptosis.

Authors:  Jia-An Zhang; Chao Luan; Dan Huang; Mei Ju; Kun Chen; Heng Gu
Journal:  Drug Des Devel Ther       Date:  2020-01-29       Impact factor: 4.162

  3 in total

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