نتایج جستجو برای: kras

تعداد نتایج: 7276  

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2015
Chen Wu Sihan Wang Caihua Xu Andreas Tyler Xingru Li Charlotta Andersson Yusuke Oji Haruo Sugiyama Yijiang Chen Aihong Li

BACKGROUND A novel link between oncogenic KRAS signalling and WT1 was recently identified. We sought to investigate the role of WT1 and KRAS in proliferation and apoptosis. METHODS KRAS mutations and WT1 (cMyc) expression were detected using Sanger sequencing and real-time PCR in 77 patients with non-small cell lung cancer (NSCLC). Overexpression and knockdown of WT1 were generated with plasm...

Journal: :Cancer research 2011
Carol Babij Yihong Zhang Robert J Kurzeja Anke Munzli Amro Shehabeldin Manory Fernando Kim Quon Paul D Kassner Astrid A Ruefli-Brasse Vivienne J Watson Flordeliza Fajardo Angela Jackson James Zondlo Yu Sun Aaron R Ellison Cherylene A Plewa Miguel Tisha San John Robinson John McCarter Ralf Schwandner Ted Judd Josette Carnahan Isabelle Dussault

Despite the prevalence of KRAS mutations in human cancers, there remain no targeted therapies for treatment. The serine-threonine kinase STK33 has been proposed to be required for the survival of mutant KRAS-dependent cell lines, suggesting that small molecule kinase inhibitors of STK33 may be useful to treat KRAS-dependent tumors. In this study, we investigated the role of STK33 in mutant KRAS...

2017
Inna Chen Victoria M. Raymond Jennifer A. Geis Eric A. Collisson Benny V. Jensen Kirstine L. Hermann Mark G. Erlander Margaret Tempero Julia S. Johansen

Precision oncology requires sensitive and specific clinical biomarkers. Carbohydrate Antigen 19-9 (CA19-9) is widely used in pancreatic ductal adenocarcinoma (PDA) but lacks sensitivity and specificity. Nearly all PDAs harbor somatic KRAS mutations, nominating circulating tumor DNA (ctDNA) KRAS as an alternative disease biomarker, however, variable clinical performance has limited its clinical ...

Journal: :Molecular cancer research : MCR 2015
Koichi Okamoto Aziz Zaanan Hisato Kawakami Shengbing Huang Frank A Sinicrope

UNLABELLED KRAS mutations are frequently detected in human colorectal cancer and contribute to de novo apoptosis resistance and ultimately therapeutic failure. To overcome KRAS-mediated apoptosis resistance, the irreversible proteasome inhibitor, carfilzomib, was evaluated and found to potently induce Noxa, which was dependent upon c-Myc, and Bik. Isogenic mutant versus wild-type KRAS carcinoma...

2016
Kosuke Toda Kenji Kawada Masayoshi Iwamoto Susumu Inamoto Takehiko Sasazuki Senji Shirasawa Suguru Hasegawa Yoshiharu Sakai

A number of clinical trials have shown that KRAS mutations of colorectal cancer (CRC) can predict a lack of responses to anti-epidermal growth factor receptor-based therapy. Recently, there have been several studies to elucidate metabolism reprogramming in cancer. However, it remains to be investigated how mutated KRAS can coordinate the metabolic shift to sustain CRC tumor growth. In this stud...

Background: Mutations in the EGFR signaling pathway play an important role in the development of colorectal cancer (CRC). Mutations in these genes, like KRAS and BRAF, affect the treatment strategies and associated with poor prognosis and relative resistance to anti-EGFR therapies. Our aim was to conduct a systematic and meta-analysis on all studies that have been conducted on the prevalence of...

2013
Ibrahim Halil Sahin Syed M.A. Kazmi Jeffrey T. Yorio Nishin A. Bhadkamkar Bryan K. Kee Christopher R. Garrett

KRAS mutations occur frequently in colorectal cancers (CRC) and predict lack of response to anti-epidermal growth factor receptor (EGFR) monoclonal antibody therapy. CRC BRAF mutations, most commonly at V600E, occur less than 10% of the time, and occur usually in KRAS wild-type tumors, and more frequently in microsatellite instable tumors. Concomitant KRAS and BRAF mutant CRCs are rare (occurri...

2013
Peter M. K. Westcott Minh D. To

Mutational activation of KRAS is a common oncogenic event in lung cancer and other epithelial cancer types. Efforts to develop therapies that counteract the oncogenic effects of mutant KRAS have been largely unsuccessful, and cancers driven by mutant KRAS remain among the most refractory to available treatments. Studies undertaken over the past decades have produced a wealth of information rega...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2010
Hans Prenen Sabine Tejpar Eric Van Cutsem

The introduction of new cytotoxic agents and new targeted therapies has significantly broadened the therapeutic options for and the outcomes of patients with metastatic colorectal cancer (CRC). The introduction of the anti-epidermal growth factor receptor (EGFR) antibodies, cetuximab and panitumumab, has clearly contributed to this development. The concept of KRAS as a marker for resistance to ...

2015
Valerie R Wiersma Marco de Bruyn Yunwei Wei Robert J van Ginkel Mitsuomi Hirashima Toshiro Niki Nozomu Nishi Jin Zhou Simon D Pouwels Douwe F Samplonius Hans W Nijman Paul Eggleton Wijnand Helfrich Edwin Bremer

Oncogenic mutation of KRAS (Kirsten rat sarcoma viral oncogene homolog) in colorectal cancer (CRC) confers resistance to both chemotherapy and EGFR (epidermal growth factor receptor)-targeted therapy. We uncovered that KRAS mutant (KRAS(mut)) CRC is uniquely sensitive to treatment with recombinant LGALS9/Galectin-9 (rLGALS9), a recently established regulator of epithelial polarity. Upon treatme...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید