نتایج جستجو برای: ژن kras

تعداد نتایج: 23037  

2017
Jung Han Kim Hyeong Su Kim Bum Jun Kim

Immune checkpoint inhibitors (ICIs) have emerged as a promising treatment option in the fight against advanced non-small-cell lung cancer (NSCLC). KRAS is the most frequently mutated oncogene in NSCLC. We performed this meta-analysis to investigate if KRAS mutation status affects survival benefits of ICIs in patients with advanced NSCLC. Electronic databases were searched for eligible studies. ...

2015
Masayuki Hiraki Junichi Nishimura Hidekazu Takahashi Xin Wu Yusuke Takahashi Masaaki Miyo Naohiro Nishida Mamoru Uemura Taishi Hata Ichiro Takemasa Tsunekazu Mizushima Jae-Won Soh Yuichiro Doki Masaki Mori Hirofumi Yamamoto

KRAS mutations are a major cause of drug resistance to molecular-targeted therapies. Aberrant epidermal growth factor receptor (EGFR) signaling may cause dysregulation of microRNA (miRNA) and gene regulatory networks, which leads to cancer initiation and progression. To address the functional relevance of miRNAs in mutant KRAS cancers, we transfected exogenous KRAS(G12V) into human embryonic ki...

2014
Radhashree Maitra Raviraja Seetharam Lydia Tesfa Titto A. Augustine Lidija Klampfer Matthew C. Coffey John M. Mariadason Sanjay Goel

Reovirus is a double stranded RNA virus, with an intrinsic preference for replication in KRAS mutant cells. As 45% of human colorectal cancers (CRC) harbor KRAS mutations, we sought to investigate its efficacy in KRAS mutant CRC cells, and examine its impact in combination with the topoisimerase-1 inhibitor, irinotecan. Reovirus efficacy was examined in the KRAS mutant HCT116, and the isogenic ...

2015
Yanzhao Wang Fuming Lei Wanshui Rong Qingmin Zeng Wenbing Sun

Approximately 30%-50% of colorectal cancers (CRCs) harbor the somatic mutated KRAS gene. KRAS G12V, one of the most common KRAS mutations in CRCs, is linked to increased tumor aggressiveness, less response to anti-epidermal growth factor receptor (EGFR) therapy, and poor survival rate. In this study, we sought to determine whether resistance to EGFR inhibitors in colorectal cancer cells harbori...

Journal: :Cancer discovery 2016
Matthew P Patricelli Matthew R Janes Lian-Sheng Li Rasmus Hansen Ulf Peters Linda V Kessler Yuching Chen Jeff M Kucharski Jun Feng Tess Ely Jeffrey H Chen Sarah J Firdaus Anjali Babbar Pingda Ren Yi Liu

UNLABELLED KRAS gain-of-function mutations occur in approximately 30% of all human cancers. Despite more than 30 years of KRAS-focused research and development efforts, no targeted therapy has been discovered for cancers with KRAS mutations. Here, we describe ARS-853, a selective, covalent inhibitor of KRAS(G12C) that inhibits mutant KRAS-driven signaling by binding to the GDP-bound oncoprotein...

2017
Jing Pan Qi Zhang Shizuko Sei Robert H. Shoemaker Ronald A. Lubet Yian Wang Ming You

Lung cancer remains the leading cause of cancer death worldwide. Mutations in KRAS are detected in up to 30% of lung cancer cases. No effective therapies specifically targeting mutant KRAS have been developed. Vaccination against KRAS mutants is one of the venues of active exploration. The present study evaluated both immunogenicity and antitumor efficacy of a newly formulated multipeptide vacc...

2012
Yu-Lin Lin Jau-Yu Liau Shan-Chi Yu Da-Liang Ou Liang-In Lin Li-Hui Tseng Yih-Leong Chang Kun-Huei Yeh Ann-Lii Cheng

Molecular biomarkers to determine the effectiveness of targeted therapies in cancer treatment have been widely adopted in colorectal cancer (CRC), but those to predict chemotherapy sensitivity remain poorly defined. We tested our hypothesis that KRAS mutation may be a predictor of oxaliplatin sensitivity in CRC. KRAS was knocked-down in KRAS-mutant CRC cells (DLD-1(G13D) and SW480(G12V)) by sma...

2014
Florian Kopp Ernst Wagner Andreas Roidl

The GTPase K-ras is involved in a variety of cellular processes such as differentiation, proliferation and survival. However, activating mutations, which frequently occur in many types of cancer, turn KRAS into one of the most prominent oncogenes. Likewise, miR-200c is a key player in tumorigenesis functioning as a molecular switch between an epithelial, non-migratory, chemosensitive and a mese...

Journal: :Anticancer research 2010
Pascale Mariani Marick Lae Armelle Degeorges Wulfran Cacheux Emmanuelle Lappartient Audrey Margogne Jean-Yves Pierga Véronique Girre Laurent Mignot Marie Christine Falcou Rémy-Jacques Salmon Olivier Delattre Patricia De Cremoux

KRAS somatic mutations are the main predictive factor for non response to EGFR-targeted monoclonal antibodies in metastatic colorectal cancer (mCRC) patients. We compared KRAS mutational status in the primary tumour and the corresponding metastases (1 to 4 sites) in 38 mCRC patients. KRAS mutational status was analysed using direct sequencing, SNAPShot multiplex PCR and Scorpion Taqman PCR anal...

Journal: :Cell 2014
Avnish Kapoor Wantong Yao Haoqiang Ying Sujun Hua Alison Liewen Qiuyun Wang Yi Zhong Chang-Jiun Wu Anguraj Sadanandam Baoli Hu Qing Chang Gerald C. Chu Ramsey Al-Khalil Shan Jiang Hongai Xia Eliot Fletcher-Sananikone Carol Lim Gillian I. Horwitz Andrea Viale Piergiorgio Pettazzoni Nora Sanchez Huamin Wang Alexei Protopopov Jianhua Zhang Timothy Heffernan Randy L. Johnson Lynda Chin Y. Alan Wang Giulio Draetta Ronald A. DePinho

Activating mutations in KRAS are among the most frequent events in diverse human carcinomas and are particularly prominent in human pancreatic ductal adenocarcinoma (PDAC). An inducible Kras(G12D)-driven mouse model of PDAC has established a critical role for sustained Kras(G12D) expression in tumor maintenance, providing a model to determine the potential for and the underlying mechanisms of K...

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