نتایج جستجو برای: mdm2 snp309

تعداد نتایج: 4579  

Journal: :European journal of haematology 2015
Ingrid Jakobsen Falk Kerstin Willander Roza Chaireti Johan Lund Hareth Nahi Monica Hermanson Henrik Gréen Kourosh Lotfi Peter Söderkvist

BACKGROUND TP53 is commonly mutated in several cancers and confers treatment resistance and poor prognosis. Altered expression of mouse double minute 2 (MDM2), a negative regulator of p53, may also attenuate normal p53 signaling, thereby enhancing tumor transformation and resistance to apoptosis. The single nucleotide polymorphism (SNP) 309 has been reported to increase MDM2 expression and impa...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2009
Elnaz F Firoz Melanie Warycha Jan Zakrzewski Danuta Pollens Guimin Wang Richard Shapiro Russell Berman Anna Pavlick Prashiela Manga Harry Ostrer Julide Tok Celebi Hideko Kamino Farbod Darvishian Linda Rolnitzky Judith D Goldberg Iman Osman David Polsky

PURPOSE In certain cancers, MDM2 SNP309 has been associated with early tumor onset in women. In melanoma, incidence rates are higher in women than in men among individuals less than 40 years of age, but among those older than 50 years of age, melanoma is more frequent in men than in women. To investigate this difference, we examined the association among MDM2 SNP309, age at diagnosis, and gende...

2008
Kathryn Terry Monica McGrath I-Min Lee Julie Buring Immaculata De Vivo

Mouse double-minute 2 homologue (MDM2) is a key negative regulator of p53, a tumor suppressor gene that initiates cell cycle arrest and apoptosis in response to DNA damage and other cellular stresses. A T > G polymorphism found in the promoter region of MDM2 (SNP309) increases MDM2 expression and thereby attenuates p53 activity. We genotyped the MDM2 polymorphism SNP309 in endometrial cancer ca...

Journal: :Neoplasma 2012
J A Machado-Neto F Traina P De Melo Campos M F Andreoli-Risso F F Costa S T Olalla Saad

MDM2/p53 pathway plays an important role in the control of apoptotic and proliferation mechanisms, and alterations in this pathway have been described in myelodysplastic syndromes (MDS). We investigated the frequency of MDM2 SNP309, TP53 Arg72Pro polymorphisms in de novo MDS and the association of these polymorphisms with clinical characteristics. Our results showed that the frequencies of geno...

Journal: :Oncotarget 2015
Melissa Rosso Alla Polotskaia Jill Bargonetti

A single nucleotide polymorphism (T to G) in the mdm2 P2 promoter, mdm2 SNP309, leads to MDM2 overexpression promoting chemotherapy resistant cancers. Two mdm2 G/G SNP309 cancer cell lines, MANCA and A875, have compromised wild-type p53 that co-localizes with MDM2 on chromatin. We hypothesized that MDM2 in these cells inhibited transcription initiation at the p53 target genes p21 and puma. Surp...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2007
Hiroshi Hirata Yuji Hinoda Nobuyuki Kikuno Ken Kawamoto Yutaka Suehiro Yuichiro Tanaka Rajvir Dahiya

PURPOSE MDM2 is a major negative regulator of p53, and a single nucleotide polymorphism in the MDM2 promoter region SNP309 (rs2279744) has been shown to increase the affinity of the transcriptional activator Sp1, resulting in elevated MDM2 transcription and expression in some cancers. There is currently no information about the role of MDM2 polymorphism in renal cell carcinoma (RCC). We investi...

2015
Linguo Xie Yan Sun Tao Chen Dawei Tian Yujuan Li Yu Zhang Na Ding Zhonghua Shen Hao Xu Xuewu Nian Nan Sha Ruifa Han Hailong Hu Changli Wu

OBJECTIVE Human murine double minute 2 protein (MDM2) is mainly a negative regulator of p53 tumor suppressor pathway. We aimed to investigate the association between MDM2 SNP309 polymorphism and bladder cancer risk. METHODS A total of 535 bladder cancer patients and 649 health controls were recruited for our study. MDM2 SNP309 T>G polymorphism was genotyped by polymerase chain reaction-ligase...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2011
Moriko Ito Louise Barys Terence O'Reilly Sophie Young Bella Gorbatcheva John Monahan Sabine Zumstein-Mecker Peter F Choong Ian Dickinson Philip Crowe Christine Hemmings Jayesh Desai David M Thomas Joanna Lisztwan

PURPOSE Reactivation of p53 tumor suppressor activity in diseases such as soft-tissue sarcoma is considered an attractive means of targeted therapy. By systematically assessing alterations affecting the p53 pathway, we aimed to (a) classify sarcoma subtypes, (b) define a potential role in malignancy, and (c) identify potential patient biomarkers in this heterogeneous disease. EXPERIMENTAL DES...

Journal: :Cancer research 2007
Uri Tabori Sonia Nanda Harriet Druker Jodi Lees David Malkin

Li-Fraumeni syndrome (LFS) is a cancer predisposition syndrome frequently associated with germ line TP53 mutations. Unpredictable and disparate age of cancer onset is a major challenge in the management of LFS. Genetic modifiers, including the MDM2-SNP309 polymorphism, and genetic anticipation have been suggested as plausible explanations for young age of tumor onset, but the molecular mechanis...

2012
WENWU HE JIANXIONG LONG LEI XIAN FENG PANG LI SU SHIXIU WEI BO WEI YANLING HU

Lung cancer is the most common diagnosed malignancy and the leading cause of cancer-related mortality worldwide. Murine double minute 2 (MDM2) SNP309 polymorphisms have been reported to influence the risk of lung cancer. However, the published studies together with four subsequent meta-analyses have yielded contradictory results. To examine this inconsistency, we conducted a meta-analysis of 6,...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید