نتایج جستجو برای: kras

تعداد نتایج: 7276  

Journal: :Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2013
Wouter W Mellema Anne-Marie C Dingemans Erik Thunnissen Peter J F Snijders Jules Derks Daniëlle A M Heideman Robertjan Van Suylen Egbert F Smit

BACKGROUND Kirsten rat sarcoma viral oncogene homolog (KRAS) mutation is thought to be related with dismal outcome for non-small-cell lung cancer (NSCLC) patients. The role of KRAS mutation as a predictor of response to chemotherapy for patients with metastatic NSCLC is poorly understood. METHODS From a retrospective database of two university hospitals, all patients with advanced, nonsquamou...

2014
Shawna L. Organ Josephine Hai Nikolina Radulovich Christopher B. Marshall Lisa Leung Takehiko Sasazuki Senji Shirasawa Chang-Qi Zhu Roya Navab Mitsuhiko Ikura Ming-Sound Tsao

KRAS is mutated in ∼40% of colorectal cancer (CRC), and there are limited effective treatments for advanced KRAS mutant CRC. Therefore, it is crucial that downstream mediators of oncogenic KRAS continue to be studied. We identified p190RhoGAP as being phosphorylated in the DLD1 CRC cell line, which expresses a heterozygous KRAS G13D allele, and not in DKO4 in which the mutant allele has been de...

Journal: :Cancer cell 2013
Ryan B Corcoran Katherine A Cheng Aaron N Hata Anthony C Faber Hiromichi Ebi Erin M Coffee Patricia Greninger Ronald D Brown Jason T Godfrey Travis J Cohoon Youngchul Song Eugene Lifshits Kenneth E Hung Toshi Shioda Dora Dias-Santagata Anurag Singh Jeffrey Settleman Cyril H Benes Mari Mino-Kenudson Kwok-Kin Wong Jeffrey A Engelman

KRAS is the most commonly mutated oncogene, yet no effective targeted therapies exist for KRAS mutant cancers. We developed a pooled shRNA-drug screen strategy to identify genes that, when inhibited, cooperate with MEK inhibitors to effectively treat KRAS mutant cancer cells. The anti-apoptotic BH3 family gene BCL-XL emerged as a top hit through this approach. ABT-263 (navitoclax), a chemical i...

2012
Snjezana Dogan Ronglai Shen Daphne C Ang Melissa L Johnson Sandra P D’Angelo Paul K Paik Edyta B Brzostowski Gregory J Riely Mark G Kris Maureen F Zakowski Marc Ladanyi

Author manuscripts have been peer reviewed and accepted for publication but have not yet been edited. Abstract Purpose: The molecular epidemiology of most EGFR and KRAS mutations in lung cancer remains unclear. Experimental Design: We genotyped 3026 lung adenocarcinomas for the major EGFR (exon 19 deletions and L858R) and KRAS (G12, G13) mutations and examined correlations with demographic, cli...

Journal: :PloS one 2016
Soo Kyung Nam Sumi Yun Jiwon Koh Yoonjin Kwak An Na Seo Kyoung Un Park Duck-Woo Kim Sung-Bum Kang Woo Ho Kim Hye Seung Lee

BACKGROUND Anti-EGFR antibody-based treatment is an important therapeutic strategy for advanced colorectal cancer (CRC); despite this, several mutations--including KRAS, BRAF, and PIK3CA mutations, and HER2 amplification--are associated with the mechanisms underlying the development of resistance to anti-EGFR therapy. The aim of our study was to investigate the frequencies and clinical implicat...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2011
Patricia R Blank Holger Moch Thomas D Szucs Matthias Schwenkglenks

PURPOSE Monoclonal antibodies against the epidermal growth factor receptor (EGFR), such as cetuximab, have led to significant clinical benefits for metastatic colorectal cancer (mCRC) patients but have also increased treatment costs considerably. Recent evidence associates KRAS and BRAF mutations with resistance to EGFR antibodies. We assessed the cost-effectiveness of predictive testing for KR...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2011
Peter P Grimminger Peter Danenberg Kathrin Dellas Dirk Arnold Claus Rödel Jean-Pascal Machiels Karin Haustermans Annelies Debucquoy Vaneja Velenik Christine Sempoux Matej Bracko Arnulf H Hölscher Robert Semrau Dongyun Yang Kathleen Danenberg Heinz-Josef Lenz Daniel Vallböhmer

PURPOSE Phase II trials in locally advanced rectal cancer have shown that cetuximab-based neoadjuvant radiochemotherapy is feasible but without an improvement in complete pathologic response rates. Our goal was to identify patients who would benefit from cetuximab-based neoadjuvant chemoradiation measuring gene expression levels of proteins involved in tumor growth [endothelial growth factor re...

Journal: :Oncology reports 2009
Zhi-Min Liu Li-Na Liu Mei Li Qiu-Ping Zhang Shi-Hua Cheng Shen Lu

KRAS proteins play an important role in regulating cell functions. A series of studies has revealed that mutations of KRAS are involved in gastric carcinogenesis. However, mutation status of KRAS remains unclear in gastric cancer from Chinese Mainland. It has been proved that KRAS mutation associates with resistance to epidermal growth factor receptor (EGFR) inhibitors. In this study, KRAS muta...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2015
Bing Yu Stephen Swatkoski Alesia Holly Liam C Lee Valentin Giroux Chih-Shia Lee Dennis Hsu Jordan L Smith Garmen Yuen Junqiu Yue David K Ann R Mark Simpson Chad J Creighton William D Figg Marjan Gucek Ji Luo

The small GTPase KRAS is frequently mutated in human cancer and currently there are no targeted therapies for KRAS mutant tumors. Here, we show that the small ubiquitin-like modifier (SUMO) pathway is required for KRAS-driven transformation. RNAi depletion of the SUMO E2 ligase Ubc9 suppresses 3D growth of KRAS mutant colorectal cancer cells in vitro and attenuates tumor growth in vivo. In KRAS...

Journal: :CPT: pharmacometrics & systems pharmacology 2018
Edward C Stites Andrey S Shaw

KRAS has proven difficult to target pharmacologically. Two strategies have recently been described for covalently targeting the most common KRAS mutant in lung cancer, KRAS G12C. Previously, we developed a computational model of the processes that regulate Ras activation. Here, we use this model to investigate KRAS G12C covalent inhibitors. We updated the model to include Ras protein turnover, ...

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