نتایج جستجو برای: tp53

تعداد نتایج: 8206  

2009
André S Khayat Adriana C Guimarães Danielle Q Calcagno Aline D Seabra Eleonidas M Lima Mariana F Leal Mário HG Faria Silvia HB Rabenhorst Paulo P Assumpção Samia Demachki Marília AC Smith Rommel R Burbano

BACKGROUND This study evaluates the existence of numerical alterations of chromosome 17 and TP53 gene deletion in gastric adenocarcinoma. The p53 protein expression was also evaluated, as well as, possible associations with clinicopathological characteristics. METHODS Dual-color fluorescence in situ hybridization and immunostaining were performed in twenty gastric cancer samples of individual...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2009
Yoko Tabe Denise Sebasigari Linhua Jin Martina Rudelius Theresa Davies-Hill Kazunori Miyake Takashi Miida Stefania Pittaluga Mark Raffeld

PURPOSE Mantle cell lymphoma (MCL) has one of the poorest prognoses of the non-Hodgkin's lymphomas, and novel therapeutic approaches are needed. We wished to determine whether Nutlin-3, a novel small-molecule murine double minute 2 (MDM2) antagonist that efficiently activates TP53, might be effective in inducing cell death in MCL. EXPERIMENTAL DESIGN MCL cell lines with known TP53 status were...

2011
Ranjan Chrisanthar Stian Knappskog Erik Løkkevik Gun Anker Bjørn Østenstad Steinar Lundgren Terje Risberg Ingvil Mjaaland Gudbrand Skjønsberg Turid Aas Ellen Schlichting Hans E. Fjösne Arne Nysted Johan Richard Lillehaug Per Eystein Lønning

BACKGROUND TP53 mutations have been associated with resistance to anthracyclines but not to taxanes in breast cancer patients. The MDM2 promoter single nucleotide polymorphism (SNP) T309G increases MDM2 activity and may reduce wild-type p53 protein activity. Here, we explored the predictive and prognostic value of TP53 and CHEK2 mutation status together with MDM2 SNP309 genotype in stage III br...

2015
Chi Young Ok Keyur P Patel Guillermo Garcia-Manero Mark J Routbort Jie Peng Guilin Tang Maitrayee Goswami Ken H Young Rajesh Singh L Jeffrey Medeiros Hagop M Kantarjian Rajyalakshmi Luthra Sa A Wang

BACKGROUND TP53 mutation is more prevalent in therapy-related myeloid neoplasms (t-MN) than their de novo counterparts; however, the pattern of mutations involving TP53 gene in t-MN versus de novo diseases is largely unknown. METHODS We collected 108 consecutive patients with therapy-related myelodysplastic syndrome (t-MDS)/acute myeloid leukemia (t-AML). Clinical, hematological, and cytogene...

2013
Richard B Richardson

TP53's role as guardian of the genome diminishes with age, as the probability of mutation increases. Previous studies have shown an association between p53 gene mutations and cancer. However, the role of somatic TP53 mutations in the steep rise in cancer rates with aging has not been investigated at a population level. This relationship was quantified using the International Agency for Research...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2003
Els M J J Berns Jan G M Klijn Maxime P Look Nicolai Grebenchtchikov Rolf Vossen Harry Peters Anneke Geurts-Moespot Henk Portengen Iris L van Staveren Marion E Meijer-van Gelder Bert Bakker Fred C G J Sweep John A Foekens

PURPOSE In recent studies, we showed that TP53 gene mutation or high levels of cytosolic vascular endothelial growth factor (VEGF) in estrogen receptor (ER)-alpha-positive primary breast tumors predict a poor disease outcome for patients treated with first-line tamoxifen for advanced disease. Mutant TP53 may up-regulate VEGF, whereas, on the other hand, wild-type TP53 may decrease VEGF producti...

2013
Qiliu Peng Xianjun Lao Zhiping Chen Hao Lai Yan Deng Jian Wang Cuiju Mo Jingzhe Sui Junrong Wu Limin Zhai Shi Yang Xue Qin Shan Li

BACKGROUND The association between TP53 R72P and/or MDM2 SNP309 polymorphisms and hepatocellular carcinoma (HCC) risk has been widely reported, but results were inconsistent. To clarify the effects of these polymorphisms on HCC risk, an updated meta-analysis of all available studies was conducted. METHODS Eligible articles were identified by search of databases including PubMed, Cochrane Libr...

2018
Zahra Shajani-Yi Francine B. de Abreu Jason D. Peterson Gregory J. Tsongalis

The tumor suppressor gene TP53 is the most frequently mutated gene in human cancer. It encodes p53, a DNA-binding transcription factor that regulates multiple genes involved in DNA repair, metabolism, cell cycle arrest, apoptosis, and senescence. TP53 is associated with human cancer by mutations that lead to a loss of wild-type p53 function as well as mutations that confer alternate oncogenic f...

Journal: :international journal of reproductive biomedicine 0
mehdi nikbakht dastjerdi roshanak aboutorabi bahram eslami farsani

background: endometriosis is a female health disorder that occurs when cells from the lining of the uterus grow in other areas of the body. the cause of endometriosis is unknown. objective: the purpose of this study was to investigate tp53 gene codon 72 polymorphism in women with endometriosis and compared it with healthy samples in isfahan. materials and methods: we undertook a case-control st...

Journal: :cell journal 0

introduction: the tumor suppressor p53 protein can induce apoptosis in some cellular contexts. among the apoptosis-inducing genes, p53 has received the most attention for cancer gene therapy. in this study, the role of dendrosome and lipofectin mediated normal cdna of tp53 into molt-4, ccrf-cem(t-iymphoma) and k562 cell lines was assessed. material and methods: at first, ccrf-cem, mol t-4 and k...

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