دورية أكاديمية

TFDP3 inhibits E2F1-induced, p53-mediated apoptosis

التفاصيل البيبلوغرافية
العنوان: TFDP3 inhibits E2F1-induced, p53-mediated apoptosis
المؤلفون: Tian, Chan, Lv, Dan, Qiao, Huan, Zhang, Jun, Yin, Yan-Hui, Qian, Xiao-Ping, Wang, Yu-Ping, Zhang, Yu, Chen, Wei-Feng
المساهمون: Zhang, Y (reprint author), Peking Univ, Hlth Sci Ctr, Dept Immunol, 38 Xue Yuan Rd, Beijing 100083, Peoples R China., Peking Univ, Hlth Sci Ctr, Dept Immunol, Beijing 100083, Peoples R China., Peking Univ, Hlth Sci Ctr, Dept Pathol, Beijing 100871, Peoples R China., Peking Univ, Hlth Sci Ctr, Dept Immunol, 38 Xue Yuan Rd, Beijing 100083, Peoples R China.
المصدر: PubMed ; SCI
بيانات النشر: 生物化学与生物物理学研究通讯
سنة النشر: 2007
المجموعة: Peking University Institutional Repository (PKU IR) / 北京大学机构知识库
مصطلحات موضوعية: TFDP3, E2F1, DP, apoptosis, p53, S-PHASE ENTRY, E2F FAMILY, CELL-CYCLE, E2F-1-INDUCED APOPTOSIS, DEREGULATED EXPRESSION, DNA-SYNTHESIS, PROTEINS, PROLIFERATION
الوصف: By dimerizing with E2F proteins, TFDP has profound influence on cellular E2F activities. While TFDPI and 2 enhance the DNA binding and the transcriptional activity of E2F, the newly identified member of the DP family, TFDP3 primarily functions as a negative regulator. To further characterize the inhibitory property of TFDP3, the present study specifically examined the modulatory role of TFDP3 on E2F1-induced cell death. HEK-293 cells underwent apoptosis following ectopic expression of E2F1. This effect was virtually abolished by co-transfection with TFDP3. In the meantime, the accumulation of p53 proteins and the increased expression of the proapoptotic molecules, including Bax, Puma, Noxa, and Bid were found to be suppressed. These data suggest a new mechanism for the regulation of E2F1-induced apoptosis and provide further evidence for the general involvement of TFDP3 in the regulation of E2F functions. (c) 2007 Elsevier Inc. All rights reserved. ; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000248659000004&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701Test ; Biochemistry & Molecular Biology ; Biophysics ; SCI(E) ; PubMed ; 13 ; ARTICLE ; 1 ; 20-25 ; 361
نوع الوثيقة: journal/newspaper
اللغة: English
تدمد: 0006-291X
17632080
العلاقة: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS.2007,361,(1),20-25.; 673027; http://hdl.handle.net/20.500.11897/198022Test; WOS:000248659000004
DOI: 10.1016/j.bbrc.2007.06.128
الإتاحة: https://doi.org/20.500.11897/198022Test
https://doi.org/10.1016/j.bbrc.2007.06.128Test
https://hdl.handle.net/20.500.11897/198022Test
رقم الانضمام: edsbas.A8209868
قاعدة البيانات: BASE
الوصف
تدمد:0006291X
17632080
DOI:10.1016/j.bbrc.2007.06.128