نتایج جستجو برای: ژن mdm2

تعداد نتایج: 20327  

Journal: :The EMBO journal 2005
Chiharu Uchida Seiichi Miwa Kyoko Kitagawa Takayuki Hattori Tomoyasu Isobe Sunao Otani Toshiaki Oda Haruhiko Sugimura Takehiko Kamijo Keizou Ookawa Hideyo Yasuda Masatoshi Kitagawa

Retinoblastoma gene product (pRB) plays critical roles in regulation of the cell cycle and tumor suppression. It is known that downregulation of pRB can stimulate carcinogenesis via abrogation of the pRB pathway, although the mechanism has not been elucidated. In this study, we found that Mdm2, a ubiquitin ligase for p53, promoted ubiquitin-dependent degradation of pRB. pRB was efficiently ubiq...

Journal: :Cancer cell 2016
Lubing Gu Hailong Zhang Tao Liu Sheng Zhou Yuhong Du Jing Xiong Sha Yi Cheng-Kui Qu Haian Fu Muxiang Zhou

MDM2 and XIAP are mutually regulated. Binding of MDM2 RING protein to the IRES region on XIAP mRNA results in MDM2 protein stabilization and enhanced XIAP translation. In this study, we developed a protein-RNA fluorescence polarization (FP) assay for high-throughput screening (HTS) of chemical libraries. Our FP-HTS identified eight inhibitors that blocked the MDM2 protein-XIAP RNA interaction, ...

2016
Jiang-Jiang Qin Wei Wang Sushanta Sarkar Sukesh Voruganti Rajesh Agarwal Ruiwen Zhang

The transcription factor NFAT1 and the oncogene MDM2 have crucial roles in breast cancer development, progression, and metastasis. We have recently discovered that NFAT1 activates MDM2 expression. Here, we identified a small molecule (named Inulanolide A) that dually inhibited both NFAT1 and MDM2 in breast cancer cells in vitro and in vivo. Unlike conventional MDM2 inhibitors, Inulanolide A (In...

2017
Shuxia Liu Yizhao Geng Shiwei Yan

About half of human cancers show normal TP53 gene and aberrant overexpression of Mdm2 and/or MdmX. This fact promotes a promising cancer therapeutic strategy which targeting the interactions between p53 and Mdm2/MdmX. For developing the inhibitors to disrupt the p53Mdm2/MdmX interactions, we systematically investigate structural and interaction characteristics of p53 and inhibitors with Mdm2 an...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 1998
R D Meng H Shih N S Prabhu D L George W S el-Deiry

Oncoprotein MDM2 inhibits p53-dependent cell cycle arrest and apoptosis. MDM2-overexpressing human cancer cell lines (n = 3) were found to be resistant to growth inhibition after infection by p53-expressing adenovirus (Ad-p53), as compared to low MDM2-expressing tumors (n = 3), in vitro. The growth of MDM2-overexpressing tumors, however, was inhibited by p21-expressing adenovirus (Ad-p21) infec...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2006
Robert C Millikan Kimberley Heard Scott Winkel Edgar J Hill Kristin Heard Beri Massa Lydia Mayes Patricia Williams Rachel Holston Kathleen Conway Sharon Edmiston Allan René de Cotret

MDM2, a protein that binds and inactivates the tumor suppressor p53, is overexpressed in a variety of human cancers (1). Bond et al. (2) recently identified a single nucleotide polymorphism in the MDM2 gene, 309 T/G within the MDM2 promoter (database for single nucleotide polymorphism reference sequence number 2279744; http:// snp500cancer.nci.nih.gov). The G allele showed increased affinity fo...

Journal: :Cell 2000
Thomas Buschmann Serge Y Fuchs Chee-Gun Lee Zhen-Qiang Pan Ze'ev Ronai

Mdm2 is an E3 ubiquitin ligase for the p53 tumor suppressor protein. We demonstrate that Mdm2 is conjugated with SUMO-1 (sumoylated) at Lys-446, which is located within the RING finger domain and plays a critical role in Mdm2 self-ubiquitination. Whereas mutant Mdm2(K446R) is stabilized, it elicits increased degradation of p53 and concomitant inhibition of p53-mediated apoptosis. In vitro sumoy...

Journal: :Oral oncology 2009
Sharifah Hamid Yi-Hsin Yang Karen Ng Lee Peng Siti Mazlipah Ismail Rosnah Binti Zain Kue Peng Lim Wan Mahadzir Wan Mustafa Mannil Thomas Abraham Soo-Hwang Teo Sok Ching Cheong

The MDM2 SNP309 has been associated with increased expression of the protein which could suppress p53 function, and has been shown to modulate risk to cancer. We have previously shown that overexpression of MDM2 is a common event in oral cancers. In the present study, we determined the association between the MDM2 SNP309 polymorphism and oral cancer in 207 oral cancer patients and 116 normal su...

2013
Xiaofeng Chen Jinrong Qiu Dapeng Yang Jianlei Lu Caiyun Yan Xiaoming Zha Yongmei Yin

The molecular mechanisms that underpin invasive ductal breast cancer (IDC) invasion and metastasis are incompletely understood. The oncogene, mouse double minute 2 (MDM2), has been implicated in the pathogenesis of numerous cancers, where it stimulates the expression of matrix metalloproteinase 9 (MMP9), an important enzyme in the breakdown of the extracellular matrix. However, its role in brea...

Journal: :Blood 2002
Lubing Gu Harry W Findley Muxiang Zhou

MDM2 protein is thought to exhibit tumorigenic activity by binding to the p53 tumor-suppressor protein and inhibiting its function. Alternatively, MDM2 may have oncogenic roles other than those resulting from p53 interactions. Here we report that MDM2 can induce expression of the p65 subunit of NF-kappaB, which is an anti-apoptotic factor expressed in certain neoplastic cells in response to che...

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