نتایج جستجو برای: mdm2 oncoprotein

تعداد نتایج: 9209  

2013
Yujun Zhao Denzil Bernard Shaomeng Wang

Inactivation of the function of tumor suppressor p53 is common in human cancers. In approximately half of human cancers, the tumor suppressor function of p53 is inactivated by deletion or mutation of TP53, the gene encoding p53 protein. In the remaining 50% of human cancers, p53 tumor suppressor function can be effectively inhibited by oncoprotein MDM2 or its homolog MDMX. Since inhibition of p...

Journal: :The Biochemical journal 2001
M Hjerrild D Milne N Dumaz T Hay O G Issinger D Meek

Murine double minute clone 2 oncoprotein (MDM2) is a key component in the regulation of the tumour suppressor p53. MDM2 mediates the ubiqutination of p53 in the capacity of an E3 ligase and targets p53 for rapid degradation by the proteasome. Stress signals which impinge on p53, leading to its activation, promote disruption of the p53-MDM2 complex, as in the case of ionizing radiation, or block...

2013
Barbara Costa Sara Bendinelli Pamela Gabelloni Eleonora Da Pozzo Simona Daniele Fabrizio Scatena Renato Vanacore Pietro Campiglia Alessia Bertamino Isabel Gomez-Monterrey Daniela Sorriento Carmine Del Giudice Guido Iaccarino Ettore Novellino Claudia Martini

Cancer development and chemo-resistance are often due to impaired functioning of the p53 tumor suppressor through genetic mutation or sequestration by other proteins. In glioblastoma multiforme (GBM), p53 availability is frequently reduced because it binds to the Murine Double Minute-2 (MDM2) oncoprotein, which accumulates at high concentrations in tumor cells. The use of MDM2 inhibitors that i...

2013
Jin Zhang Enshun Xu Xinbin Chen

The murine double minute-2 (Mdm2) oncoprotein is an E3 ligase and a key regulator of a variety of fundamental cellular processes [1]. Mdm2 was originally identified as being amplified on double-minute chromosomes in transformed mouse fibroblasts [2]. Soon after its discovery, Mdm2 was found to be a negative regulator of tumor suppressor p53. The importance of Mdm2 in controlling the p53 activit...

2016
Anusha Sriraman Marija Radovanovic Magdalena Wienken Zeynab Najafova Yizhu Li Matthias Dobbelstein

Targeting the Mdm2 oncoprotein by drugs has the potential of re-establishing p53 function and tumor suppression. However, Mdm2-antagonizing drug candidates, e. g. Nutlin-3a, often fail to abolish cancer cell growth sustainably. To overcome these limitations, we inhibited Mdm2 and simultaneously a second negative regulator of p53, the phosphatase Wip1/PPM1D. When combining Nutlin-3a with the Wip...

Journal: :Biomedical reports 2017
Ayca Tas Mustafa Atabey Gulcin Caglayan Meric Emre Bostanci Serap Sahin Bolukbasi Omer Topcu Yavuz Silig

Murine double minute clone 2 oncoprotein (MDM2) is a key component in the regulation of the tumour suppressor p53. The association between the MDM2 polymorphism and gastric cancer (GC) has been investigated in Turkish population. In the present case-control study, the aim was to investigate the association between genetic polymorphisms of the MDM2 gene (a major regulator of p53 function) and pr...

2014
Mohammad Hashemi Mohsen Omrani Ebrahim Eskandari-Nasab Seyed-Shahaboddin Hasani Mohammad Ali Mashhadi Mohsen Taheri

BACKGROUND MDM2 (Murine Double Minute2) is an oncoprotein that inhibits the P53 activity. Overexpression of MDM2 gene has been reported in several human tumors. In the present study, we aimed to evaluate the impact of 40-bp insertion/deletion (ins/del) polymorphism on the promoter of MDM2 and susceptibility to breast cancer in a sample of Iranian population. METHODS This case-control study wa...

Journal: :International journal of oncology 2007
Akihiro Katayama Takeshi Ogino Nobuyuki Bandoh Miki Takahara Kan Kishibe Satoshi Nonaka Yasuaki Harabuchi

The purpose of this research was to identify a molecular clue to tumor proliferation in oral squamous cell carcinoma (SCC) and to test the value as a predictive marker for prognosis. In cDNA array analysis, small ubiquitin-related modifier-1 (SUMO-1) was expressed at much higher levels in oral SCC tissue and oral SCC cell lines than normal oral epithelium. The result was confirmed by RT-PCR ana...

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