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Current Pharmaceutical Design

Editor-in-Chief

ISSN (Print): 1381-6128
ISSN (Online): 1873-4286

Proteomic-based Analysis for Identification of Proteins Involved in 5-fluorouracil Resistance in Hepatocellular Carcinoma

Author(s): Yi Tan, Shukui Qin, Xin Hou, Xiujuan Qian, Jun Xia, Yumei Li, Rui Wang, Changjie Chen, Qingling Yang, Lucio Miele, Qiong Wu andZhiwei Wang

Volume 20, Issue 1, 2014

Page: [81 - 87]Pages: 7

DOI:10.2174/138161282001140113125143

Price: $65

TIMBC 2025
Abstract

Background: Hepatocellular carcinoma (HCC) has high mortality partly due to acquiring drug resistance during chemotherapytreatment. Therefore, it is necessary to explore the underlying mechanism of drug resistance.

Methods: We used 2-DE and MALDI-TOF-MS analysis to explore the possible molecular insight into 5-FU resistance in HCC. The differentiallyexpressed proteins were validated by Western blot analysis.

Results: We identified 102 unique proteins including p16, maspin, PRDX6, PSMB7, MYL6, PHB, and HSP27 with alteration in SMMC-7721/5-FU. Furthermore, down-regulation of PRDX6 and PSMB7 enhanced SMMC-7721/5-FU cells to 5-FU sensitivity.

Conclusions: Our study suggests that targeting drug resistant genes such as PRDX6 and PSMB7 could be a novel approach to overcome5-FU resistance in HCC cells.

Keywords:Hepatocellular carcinoma, chemoresistance, 5-FU, PRDX6, PMSB7.


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Current Pharmaceutical Design

Title:Proteomic-based Analysis for Identification of Proteins Involved in 5-fluorouracil Resistance in Hepatocellular Carcinoma

Volume: 20Issue: 1

Author(s):Yi Tan, Shukui Qin, Xin Hou, Xiujuan Qian, Jun Xia, Yumei Li, Rui Wang, Changjie Chen, Qingling Yang, Lucio Miele, Qiong Wu and Zhiwei Wang

Affiliation:

                          Keywords:Hepatocellular carcinoma, chemoresistance, 5-FU, PRDX6, PMSB7.

                          Abstract: Background: Hepatocellular carcinoma (HCC) has high mortality partly due to acquiring drug resistance during chemotherapytreatment. Therefore, it is necessary to explore the underlying mechanism of drug resistance.

                          Methods: We used 2-DE and MALDI-TOF-MS analysis to explore the possible molecular insight into 5-FU resistance in HCC. The differentiallyexpressed proteins were validated by Western blot analysis.

                          Results: We identified 102 unique proteins including p16, maspin, PRDX6, PSMB7, MYL6, PHB, and HSP27 with alteration in SMMC-7721/5-FU. Furthermore, down-regulation of PRDX6 and PSMB7 enhanced SMMC-7721/5-FU cells to 5-FU sensitivity.

                          Conclusions: Our study suggests that targeting drug resistant genes such as PRDX6 and PSMB7 could be a novel approach to overcome5-FU resistance in HCC cells.

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                          Cite this article as:

                          Tan Yi, Qin Shukui, Hou Xin, Qian Xiujuan, Xia Jun, Li Yumei, Wang Rui, Chen Changjie, Yang Qingling, Miele Lucio, Wu Qiong and Wang Zhiwei, Proteomic-based Analysis for Identification of Proteins Involved in 5-fluorouracil Resistance in Hepatocellular Carcinoma, Current Pharmaceutical Design 2014; 20 (1) .https://dx.doi.org/10.2174/138161282001140113125143

                          DOI
                          https://dx.doi.org/10.2174/138161282001140113125143
                          Print ISSN
                          1381-6128
                          Publisher Name
                          Bentham Science Publisher
                          Online ISSN
                          1873-4286

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