نتایج جستجو برای: p53 polymorphism

تعداد نتایج: 148550  

Journal: :Cancer research 1998
T Minaguchi Y Kanamori M Matsushima H Yoshikawa Y Taketani Y Nakamura

Human papillomavirus (HPV)-16 and -18 encode E6 oncoprotein, which binds to and induces degradation of the tumor suppressor protein p53. A common polymorphism of p53, encoding either proline or arginine at position 72, affects the susceptibility of p53 to E6-mediated degradation in vivo; Caucasian women homozygous for arginine 72 reportedly are about seven times more susceptible to HPV-associat...

Journal: :Oncology reports 2007
Annette Pantelis Dimitrios Pantelis Petra Ruemmele Arndt Hartmann Ferdinand Hofstaedter Reinhard Buettner Friedrich Bootz Robert Stoehr

Epidemiological studies in endemic geographic regions for esophageal squamous cell carcinoma (ESCC) suggested a number of risk factors, including modifications of the p53 tumor suppressor by codon Arg72Pro polymorphism, loss of heterozygosity (LOH) or human papillomavirus type 16 or 18 (HPV 16/18) infection. The p53 Arg72 variant has been suggested to be a high-risk factor in HPV-associated tum...

Journal: :Journal of medical genetics 2005
D P Dimasi A W Hewitt C M Green D A Mackey J E Craig

BACKGROUND The final common pathway for open angle glaucoma (OAG) is retinal ganglion cell apoptosis. Polymorphisms in p53, a major regulator of apoptosis, affect the efficiency of cell death induction. Association studies of p53 haplotypes and OAG have had conflicting results. OBJECTIVE To examine the association between p53 haplotypes and OAG in a larger white population than in previous re...

Journal: :Cancer research 1991
R J Osborne G R Merlo T Mitsudomi T Venesio D S Liscia A P Cappa I Chiba T Takahashi M M Nau R Callahan

Twenty-six primary breast tumors were examined for mutations in the p53 tumor suppressor gene by an RNase protection assay and nucleotide sequence analysis of PCR-amplified p53 complementary DNAs. Each method detected p53 mutations in the same three tumors (12%). One tumor contained two mutations in the same allele. Single strand conformation polymorphism analysis of genomic DNA and complementa...

Journal: :Genetics and molecular research : GMR 2008
P S R Almeida W J Manoel A A S Reis E R Silva E Martins M V O Paiva A C Fraga V A Saddi

Soft tissue sarcomas (STS) are tumors of mesodermal origin, comprising about 1% of all adult neoplasms. Management of such tumors is an important medical challenge. TP53 codon 72 polymorphism results in either the arginine or proline form of the p53 protein; several studies have investigated whether codon 72 polymorphisms are risk and prognostic factors for cancer. We investigated p53 codon 72 ...

Journal: :Japanese journal of clinical oncology 2011
Amit Man Joshi Sanjeev Budhathoki Keizo Ohnaka Ryuichi Mibu Masao Tanaka Yoshihiro Kakeji Yoshihiko Maehara Takeshi Okamura Koji Ikejiri Kitaroh Futami Takafumi Maekawa Yohichi Yasunami

OBJECTIVE Tumor protein p53 gene and its negative regulator, murine double minute 2 homolog are important components for cell-cycle arrest and apoptosis. An arginine-to-proline substitution at codon 72 in the p53 gene is reported to decrease apoptotic potential, while a thymine-to-guanine polymorphism at nucleotide 309, named SNP309, of murine double minute 2 gene increases transcription of the...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2003
Ling-Ling Hsieh Huei-Tzu Chien I-How Chen Chun-Ta Liao Hung-Ming Wang Shih-Ming Jung Pei-Feng Wang Joseph Tung-Chieh Chang Min-Chi Chen Ann-Joy Cheng

DNA repair gene polymorphisms have been implicated as susceptibility factors in cancer development. It is possible that DNA repair polymorphisms may also influence the risk of gene mutation. The 399Gln polymorphism in the DNA repair gene XRCC1 has been indicated to have a contributive role in DNA adduct formation, sister chromatid exchange, and an increased risk of cancer development. Two hundr...

Journal: :Heart 2004
S Kojima N Iwai N Tago K Ono K Ohmi G Tsujimoto S Takagi S Miyazaki H Nonogi Y Goto

T he cause of in-stent luminal narrowing has been primarily considered to be neointimal hyperplasia that is caused by proliferating vascular smooth muscle cells (VSMC). It has been recently reported that local drug delivery systems produce good results for the inhibition of VSMC proliferation. The potential of suppressive agents in the treatment of in-stent luminal narrowing arises from basic s...

Journal: :BMC Urology 2005
Gustavo J Leiros Silvia R Galliano Mario E Sember Tomas Kahn Elisabeth Schwarz Kumiko Eiguchi

BACKGROUND Infections with high-risk human papillomaviruses (HPVs), causatively linked to cervical cancer, might also play a role in the development of prostate cancer. Furthermore, the polymorphism at codon 72 (encoding either arginine or proline) of the p53 tumor-suppressor gene is discussed as a possible determinant for cancer risk. The HPV E6 oncoprotein induces degradation of the p53 prote...

2014
Seema Sikka Pranav Sikka

BACKGROUND Human papillomavirus (HPV) and p53 alterations are speculated to play a role in carcinogenesis. This study was carried out to find out the association of HPV and p53 with precancerous lesions of the oral cavity such as leukoplakia: The objective of this study was to find the association among human papilloma virus (HPV) 16 infections and p53 polymorphism in tobacco using the oral leu...

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