نتایج جستجو برای: nras

تعداد نتایج: 2055  

2017
Coralie Dorard Charlène Estrada Céline Barbotin Magalie Larcher Alexandra Garancher Jessy Leloup Friedrich Beermann Manuela Baccarini Celio Pouponnot Lionel Larue Alain Eychène Sabine Druillennec

NRAS and its effector BRAF are frequently mutated in melanoma. Paradoxically, CRAF but not BRAF was shown to be critical for various RAS-driven cancers, raising the question of the role of RAF proteins in NRAS-induced melanoma. Here, using conditional ablation of Raf genes in NRAS-induced mouse melanoma models, we investigate their contribution in tumour progression, from the onset of benign tu...

2012
James G. Greger Stephen D. Eastman Vivian Zhang Maureen R. Bleam Ashley M. Hughes Kimberly N. Smitheman Scott H. Dickerson Sylvie G. Laquerre Li Liu Tona M. Gilmer

Recent results from clinical trials with the BRAF inhibitors GSK2118436 (dabrafenib) and PLX4032 (vemurafenib) have shown encouraging response rates; however, the duration of response has been limited. To identify determinants of acquired resistance to GSK2118436 and strategies to overcome the resistance, we isolated GSK2118436 drug-resistant clones from the A375 BRAF and the YUSIT1 BRAF melano...

Journal: :Molecular cancer therapeutics 2012
James G Greger Stephen D Eastman Vivian Zhang Maureen R Bleam Ashley M Hughes Kimberly N Smitheman Scott H Dickerson Sylvie G Laquerre Li Liu Tona M Gilmer

Recent results from clinical trials with the BRAF inhibitors GSK2118436 (dabrafenib) and PLX4032 (vemurafenib) have shown encouraging response rates; however, the duration of response has been limited. To identify determinants of acquired resistance to GSK2118436 and strategies to overcome the resistance, we isolated GSK2118436 drug-resistant clones from the A375 BRAF(V600E) and the YUSIT1 BRAF...

2011
Filip Janku J. Jack Lee Apostolia M. Tsimberidou David S. Hong Aung Naing Gerald S. Falchook Siqing Fu Rajyalakshmi Luthra Ignacio Garrido-Laguna Razelle Kurzrock

BACKGROUND Oncogenic mutations of PIK3CA, RAS (KRAS, NRAS), and BRAF have been identified in various malignancies, and activate the PI3K/AKT/mTOR and RAS/RAF/MEK pathways, respectively. Both pathways are critical drivers of tumorigenesis. METHODS Tumor tissues from 504 patients with diverse cancers referred to the Clinical Center for Targeted Therapy at MD Anderson Cancer Center starting in O...

Journal: :Cancer immunology research 2015
Douglas B Johnson Christine M Lovly Marisa Flavin Katherine S Panageas Gregory D Ayers Zhiguo Zhao Wade T Iams Marta Colgan Sarah DeNoble Charles R Terry Elizabeth G Berry A John Iafrate Ryan J Sullivan Richard D Carvajal Jeffrey A Sosman

Activating NRAS mutations are found in 15% to 20% of melanomas. Immune therapies have become a mainstay in advanced melanoma treatment. We sought to evaluate whether tumor genotype (e.g., NRAS mutations) correlates with benefit from immune therapy in melanoma. We identified 229 patients with melanoma treated with immune therapies [IL2, ipilimumab, or anti-programmed cell death-1/ligand-1 (PD-1/...

2018
Louise Johnston Michael Power Philip Sloan Anna Long Angela Silmon Ben Chaffey Andrea Jane Lisgo Liam Little Ellen Vercauteren Torben Steiniche Tine Meyer John Simpson

AIMS Understanding the molecular mechanisms of underlying disease has led to a movement away from the one-drug-fits-all paradigm towards treatment tailored to the genetic profile of the patient. The Biocartis Idylla platform is a novel fully automated, real-time PCR-based in vitro diagnostic system. The Idylla NRAS-BRAF mutation test has been developed for the qualitative detection of mutations...

Journal: :Oncology reports 2007
Hidefumi Sasaki Katsuhiro Okuda Osamu Kawano Katsuhiko Endo Haruhiro Yukiue Tomoki Yokoyama Motoki Yano Yoshitaka Fujii

Activating mutations of Ras gene families have been found in a variety of human malignancies, including lung cancer, suggesting their dominant role in tumorigenesis. Many studies have showed that the Kras gene is activated by point mutations in approximately 15-20% of non-small cell lung cancers (NSCLCs), however, there are only a few reports on Nras mutations in NSCLC. We have genotyped Nras m...

Journal: :Blood 2006
Ulrike Bacher Torsten Haferlach Claudia Schoch Wolfgang Kern Susanne Schnittger

We analyzed 2502 patients with acute myeloid leukemia at diagnosis for NRAS mutations around the hot spots at codons 12, 13, and 61 and correlated the results to cytomorphology, cytogenetics, other molecular markers, and prognostic relevance of these mutations. Two hundred fifty-seven (10.3%) of 2502 patients had NRAS mutations (NRAS(mut)). Most mutations (112 of 257; 43.6%) were found at codon...

Journal: :Melanoma research 2014
Inna V Fedorenko Bin Fang John M Koomen Geoffrey T Gibney Keiran S M Smalley

Effective targeted therapy strategies are still lacking for the 15-20% of melanoma patients whose melanomas are driven by oncogenic NRAS. Here, we report on the NRAS-specific behavior of amuvatinib, a kinase inhibitor with activity against c-KIT, Axl, PDGFRα, and Rad51. An analysis of BRAF-mutant and NRAS-mutant melanoma cell lines showed the NRAS-mutant cohort to be enriched for targets of amu...

Journal: :Head & neck 2016
Marisa Cañadas-Garre Patricia Becerra-Massare Antonia Moreno Casares Miguel Ángel Calleja-Hernández José Manuel Llamas-Elvira

BACKGROUND Multifocality of papillary thyroid carcinoma (PTC) is common. BRAF and NRAS mutations are the most frequent genetic alterations in PTC. The purpose of this study was to determine the distribution and relevance of BRAFT1799A and NRAS mutations in PTC. METHODS BRAFT1799A and NRAS mutations were evaluated in 195 intrathyroid or metastatic foci from 29 patients with multifocal PTC. R...

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