Data for aproteomic analysis of p53-independent induction of apoptosis by bortezomib

被引:1
|
作者
Yerlikaya, Azmi [1 ]
Okur, Emrah [2 ]
Baykal, Ahmet Tarik [3 ]
Acilan, Ceyda [4 ]
Boyaci, Ihsan [5 ]
Ulukaya, Engin [6 ]
机构
[1] Dumlupinar Univ, Fac Med, Dept Med Biol, Kutahya, Turkey
[2] Dumlupinar Univ, Art & Sci Fac, Dept Biol, Kutahya, Turkey
[3] Istanbul Medipol Univ, Sch Med, Dept Med Biochem, Istanbul, Turkey
[4] TUBITAK, MAM, Genet Engn & Biotechnol Dept, Gebze, Kocaeli, Turkey
[5] Istanbul Medipol Univ, Vatan Clin, TR-34214 Istanbul, Turkey
[6] Uludag Univ, Dept Med Biochem, Bursa, Turkey
来源
DATA IN BRIEF | 2014年 / 1卷
关键词
D O I
10.1016/j.dib.2014.09.003
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This data article contains data related to the research article entitled, A proteomic analysis of p53-independent induction of apoptosis by bortezomib in 4T1 breast cancer cell line by Yerlikaya et al. [1]. The research article presented 2-DE and nLC-MS/MS based proteomic analysis of proteasome inhibitor bortezomib-induced changes in the expression of cellular proteins. The report showed that GRP78 and TCEB2 were over-expressed in response to treatment with bortezomib for 24 h. In addition, the report demonstrated that Hsp70, the 26S proteasome non-ATPase regulatory subunit 14 and sequestosome 1 were increased at least 2 fold in p53-deficient 4T1 cells. The data here show for the first time the increased expressions of Card10, Dffb, Traf3 and Trp53bp2 in response to inhibition of the 26S proteasome. The information presented here also shows that both Traf1 and Xiap (a member of IAPs) are also downregulated simultaneously upon proteasomal inhibition. The increases in the level of Card10 and Trp53bp2 proteins were verified by Western blot analysis in response to varying concentrations of bortezomib for 24 h. (C) 2014 The Authors. Published by Elsevier Inc.
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收藏
页码:56 / 59
页数:4
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