نتایج جستجو برای: tp53 protein

تعداد نتایج: 1240012  

2016
Yu Zhang Lan Cao Daniel Nguyen Hua Lu

Genomic sequencing analyses of a variety of human cancers have revealed that massive mutations of cancer-relevant genes are the major alterations in cancerous cells, and their mutation frequencies or rates are highly associated with the development, progression, metastasis, and drug resistance of cancers as well as their clinical outcomes and prognosis. One predominant genetic alternation in hu...

Journal: :Haematologica 2010
Laurence Lodé Marion Eveillard Valérie Trichet Thierry Soussi Soraya Wuillème Steven Richebourg Florence Magrangeas Norbert Ifrah Loïc Campion Catherine Traullé François Guilhot Denis Caillot Gérald Marit Claire Mathiot Thierry Facon Michel Attal Jean-Luc Harousseau Philippe Moreau Stéphane Minvielle Hervé Avet-Loiseau

Deletion of the 17p13 chromosomal region [del(17p)] is associated with a poor outcome in multiple myeloma. Most of the studies have targeted the TP53 gene for deletion analyses, although no study showed that this gene is the deletion target. In order to address this issue, we sequenced the TP53 gene in 92 patients with multiple myeloma at diagnosis, 54 with a del(17p) and 38 lacking del(17p). A...

2017
Xiaosheng Wang Qingrong Sun

Although the associations of p53 dysfunction, p53 interaction networks and oncogenesis have been widely explored, a systematic analysis of TP53 mutations and its related interaction networks in various types of human cancers is lacking. Our study explored the associations of TP53 mutations, gene expression, clinical outcomes, and TP53 interaction networks across 33 cancer types using data from ...

2016
Netta Mäkinen Mervi Aavikko Tuomas Heikkinen Minna Taipale Jussi Taipale Riitta Koivisto-Korander Ralf Bützow Pia Vahteristo Cynthia C. Morton

Uterine leiomyosarcomas (ULMSs) are aggressive smooth muscle tumors associated with poor clinical outcome. Despite previous cytogenetic and molecular studies, their molecular background has remained elusive. To examine somatic variation in ULMS, we performed exome sequencing on 19 tumors. Altogether, 43 genes were mutated in at least two ULMSs. Most frequently mutated genes included tumor prote...

2017
Audrey Gros Elodie Laharanne Marie Vergier Martina Prochazkova-Carlotti Anne Pham-Ledard Thomas Bandres Sandrine Poglio Sabine Berhouet Béatrice Vergier Jean-Philippe Vial Edith Chevret Marie Beylot-Barry Jean-Philippe Merlio

Recent massive parallel sequencing data have evidenced the genetic diversity and complexity of Sézary syndrome mutational landscape with TP53 alterations being the most prevalent genetic abnormality. We analyzed a cohort of 35 patients with SS and a control group of 8 patients with chronic inflammatory dermatoses. TP53 status was analyzed at different clinical stages especially in 9 patients wi...

2016
Koichi Takahashi Keyur Patel Carlos Bueso-Ramos Jianhua Zhang Curtis Gumbs Elias Jabbour Tapan Kadia Michael Andreff Marina Konopleva Courtney DiNardo Naval Daver Jorge Cortes Zeev Estrov Andrew Futreal Hagop Kantarjian Guillermo Garcia-Manero

We screened TP53 mutations in 168 MDS patients who were treated with HMA and evaluated predictive and prognostic value of TP53 mutations. Overall response to HMA was not different based on TP53 mutation status (45% vs. 32% in TP53-mutated and wild type [WT], respectively, P = 0.13). However, response duration was significantly shorter in TP53-mutated patients compared to WT patients (5.7 months...

2016
Kathleen Oros Klein Karim Oualkacha Marie-Hélène Lafond Sahir Bhatnagar Patricia N. Tonin Celia M. T. Greenwood

In a variety of solid cancers, missense mutations in the well-established TP53 tumor suppressor gene may lead to the presence of a partially-functioning protein molecule, whereas mutations affecting the protein encoding reading frame, often referred to as null mutations, result in the absence of p53 protein. Both types of mutations have been observed in the same cancer type. As the resulting tu...

2016
Jincui Gu Yanbin Zhou Lixia Huang Weijun Ou Jian Wu Shaoli Li Junwen Xu Jinlun Feng Baomo Liu

A number of studies have examined the association between tumor protein 53 (TP53) mutations and the clinical outcome in patients with non-small-cell lung cancer (NSCLC), although these have yielded conflicting results. In the present study, electronic databases updated to September 2015 were searched to find relevant studies. A meta-analysis was performed on the eligible studies, which quantita...

2018
Min Bao Yingjian Song Jingjing Xia Pengling Li Qing Liu Zongren Wan

Background and aim Lung cancer is the leading cause of cancer death worldwide. In this study, we aim to elucidate the role of miR-1269 in the pathogenesis of lung cancer. Methods and results From the results of analyses using The Cancer Genome Atlas (TCGA) database, we noted the expression of miR-1269 was increased in lung cancer tissue. miR-1269 expression was detected in both the normal adj...

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