Proteomic analysis of differential proteins in pancreatic carcinomas: Effects of MBD1 knock-down by stable RNA interference

<p>Abstract</p> <p>Background</p> <p>Methyl-CpG binding domain protein 1 (MBD1), a suppressor of gene transcription, may be involved in inactivation of tumor suppressor genes during tumorigenesis. Over-expression of MBD1 has been reported in human pancreatic carcinomas....

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Main Authors: Ni Quanxing, Long Jiang, Xu Jin, Jin Chen, Yu Xianjun, Chen Yaohui, Liu Chen, Fu Deliang, Jin Hong, Bai Chen
Format: Article
Language:English
Published: BMC 2008-04-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/8/121
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spelling doaj-815340400f6c4b2f99456100b53bb89d2020-11-25T01:13:33ZengBMCBMC Cancer1471-24072008-04-018112110.1186/1471-2407-8-121Proteomic analysis of differential proteins in pancreatic carcinomas: Effects of MBD1 knock-down by stable RNA interferenceNi QuanxingLong JiangXu JinJin ChenYu XianjunChen YaohuiLiu ChenFu DeliangJin HongBai Chen<p>Abstract</p> <p>Background</p> <p>Methyl-CpG binding domain protein 1 (MBD1), a suppressor of gene transcription, may be involved in inactivation of tumor suppressor genes during tumorigenesis. Over-expression of MBD1 has been reported in human pancreatic carcinomas.</p> <p>Methods</p> <p>In this study, we established a MBD1-knock-down pancreatic cancer cell line (BxPC-3) using stable RNA interference, to compare the proteomic changes between control and MBD1-knock-down cells using two-dimensional gel electrophoresis and mass spectrometry.</p> <p>Results</p> <p>We identified five proteins that were up-regulated and nine proteins that were down-regulated. Most of the identified proteins are involved in tumorigenesis, some are prognostic biomarkers for human malignant tumors.</p> <p>Conclusion</p> <p>Our data suggest that these differential proteins may be associated with the function of MBD1, and provide some insight into the functional mechanism of MBD1 in the development of pancreatic cancer.</p> http://www.biomedcentral.com/1471-2407/8/121
collection DOAJ
language English
format Article
sources DOAJ
author Ni Quanxing
Long Jiang
Xu Jin
Jin Chen
Yu Xianjun
Chen Yaohui
Liu Chen
Fu Deliang
Jin Hong
Bai Chen
spellingShingle Ni Quanxing
Long Jiang
Xu Jin
Jin Chen
Yu Xianjun
Chen Yaohui
Liu Chen
Fu Deliang
Jin Hong
Bai Chen
Proteomic analysis of differential proteins in pancreatic carcinomas: Effects of MBD1 knock-down by stable RNA interference
BMC Cancer
author_facet Ni Quanxing
Long Jiang
Xu Jin
Jin Chen
Yu Xianjun
Chen Yaohui
Liu Chen
Fu Deliang
Jin Hong
Bai Chen
author_sort Ni Quanxing
title Proteomic analysis of differential proteins in pancreatic carcinomas: Effects of MBD1 knock-down by stable RNA interference
title_short Proteomic analysis of differential proteins in pancreatic carcinomas: Effects of MBD1 knock-down by stable RNA interference
title_full Proteomic analysis of differential proteins in pancreatic carcinomas: Effects of MBD1 knock-down by stable RNA interference
title_fullStr Proteomic analysis of differential proteins in pancreatic carcinomas: Effects of MBD1 knock-down by stable RNA interference
title_full_unstemmed Proteomic analysis of differential proteins in pancreatic carcinomas: Effects of MBD1 knock-down by stable RNA interference
title_sort proteomic analysis of differential proteins in pancreatic carcinomas: effects of mbd1 knock-down by stable rna interference
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2008-04-01
description <p>Abstract</p> <p>Background</p> <p>Methyl-CpG binding domain protein 1 (MBD1), a suppressor of gene transcription, may be involved in inactivation of tumor suppressor genes during tumorigenesis. Over-expression of MBD1 has been reported in human pancreatic carcinomas.</p> <p>Methods</p> <p>In this study, we established a MBD1-knock-down pancreatic cancer cell line (BxPC-3) using stable RNA interference, to compare the proteomic changes between control and MBD1-knock-down cells using two-dimensional gel electrophoresis and mass spectrometry.</p> <p>Results</p> <p>We identified five proteins that were up-regulated and nine proteins that were down-regulated. Most of the identified proteins are involved in tumorigenesis, some are prognostic biomarkers for human malignant tumors.</p> <p>Conclusion</p> <p>Our data suggest that these differential proteins may be associated with the function of MBD1, and provide some insight into the functional mechanism of MBD1 in the development of pancreatic cancer.</p>
url http://www.biomedcentral.com/1471-2407/8/121
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