نتایج جستجو برای: codon 72 polymorphism

تعداد نتایج: 213974  

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...

2000
Hidetoshi Kawaguchi Shinji Ohno Koshi Araki Mitsuhiro Miyazaki Hiroshi Saeki Masayuki Watanabe Shinji Tanaka Keizo Sugimachi

Human papillomavirus type 16/18 (HPV-16/18) is implicated in the pathogenesis of squamous cell carcinoma (SCC) of the cervix and esophagus. The arginine allele at codon 72 of p53 was found to be more susceptible to degradation by HPV E6 protein than is the proline allele in vivo, thus resulting in a high frequency of cervical SCC in individuals homozygous for arginine at the codon. There are co...

2013
TOMOKO YONEDA AYUMI KUBOYAMA KIYOKO KATO TATSUHIRO OHGAMI KANAKO OKAMOTO TOSHIAKI SAITO NORIO WAKE

The incidence of endometrial cancer, a common gynecological malignancy, is increasing in Japan. We have previously shown that the ER/MDM2/p53/p21 pathway plays an important role in endometrial carcinogenesis. In the present study, we investigated the effects of germline single nucleotide polymorphisms in murine double minute 2 (MDM2) SNP309, TP53 Arg72Pro, ESR1 PvuII and XbaI, and p21 codon 31 ...

Journal: :Cancer research 2000
H Kawaguchi S Ohno K Araki M Miyazaki H Saeki M Watanabe S Tanaka K Sugimachi

Human papillomavirus type 16/18 (HPV-16/18) is implicated in the pathogenesis of squamous cell carcinoma (SCC) of the cervix and esophagus. The arginine allele at codon 72 of p53 was found to be more susceptible to degradation by HPV E6 protein than is the proline allele in vivo, thus resulting in a high frequency of cervical SCC in individuals homozygous for arginine at the codon. There are co...

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: :Journal of Korean Medical Science 2000
W. K. Baek J. W. Cho S. I. Suh M. H. Suh D. H. Shin C. H. Cho T. S. Lee S. D. Cha

A common polymorphism of the wild type p53 is known at codon 72 of exon 4, with 2 alleles encoding either arginine (CGC, p53Arg) or proline (CCC, p53Pro). A recent study suggested that this polymorphism affects the susceptibility of p53 protein to human papillomavirus E6 oncoprotein mediated degradation and that individuals homozygous for p53Arg are seven times more susceptible to HPV-associate...

2003
Hiroyuki Azuma Yuka Uno Shiro Saito

We used a polymerase chain reaction (PCR) strategy and restriction fragment polymorphism analysis to evaluate all 19 exons of the plasminogen (PLG) gene in a Japanese patient with congenital PLG deficiency and her family members. She presented with cerebral infarction. Sequence analysis following amplification of each exon and its flanking regions showed a single T to C transition in exon 14, w...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2011
D Surekha K Sailaja D Nageswara Rao T Padma D Raghunadharao S Vishnupriya

The p53 protein is at the center of cell regulatory pathways influencing transcription and activity of several replication and transcription factors. In exon 4 of the gene TP53, a codon 72 polymorphism causing an Arg/Pro substitution has been reported in breast and other cancers. This substitution is in the putative SH3 binding domain of p53 protein, influencing binding capacity and thereby fun...

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