نتایج جستجو برای: vemurafenib

تعداد نتایج: 1054  

2016
Helena Escuin-Ordinas Shuoran Li Michael W Xie Lu Sun Willy Hugo Rong Rong Huang Jing Jiao Felipe Meira de-Faria Susan Realegeno Paige Krystofinski Ariel Azhdam Sara Marie D Komenan Mohammad Atefi Begoña Comin-Anduix Matteo Pellegrini Alistair J Cochran Robert L Modlin Harvey R Herschman Roger S Lo William H McBride Tatiana Segura Antoni Ribas

BRAF inhibitors are highly effective therapies for the treatment of BRAF(V600)-mutated melanoma, with the main toxicity being a variety of hyperproliferative skin conditions due to paradoxical activation of the mitogen-activated protein kinase (MAPK) pathway in BRAF wild-type cells. Most of these hyperproliferative skin changes improve when a MEK inhibitor is co-administered, as it blocks parad...

Journal: :Cancer discovery 2014
Jean M Mulcahy Levy Joshua C Thompson Andrea M Griesinger Vladimir Amani Andrew M Donson Diane K Birks Michael J Morgan David M Mirsky Michael H Handler Nicholas K Foreman Andrew Thorburn

UNLABELLED Autophagy inhibition is a potential therapeutic strategy in cancer, but it is unknown which tumors will benefit. The BRAF(V600E) mutation has been identified as important in pediatric central nervous system (CNS) tumors and is known to affect autophagy in other tumor types. We evaluated CNS tumor cells with BRAF(V600E) and found that mutant (but not wild-type) cells display high rate...

2016
Theresa M Medina Karl D Lewis

Metastatic melanoma is an aggressive, rapidly progressive disease which historically had very few effective treatment options. However, since 2011, the therapeutic landscape of melanoma has undergone a dramatic transformation with two distinct approaches and has catalyzed the successful advancement in the clinical field of immuno-oncology. In addition, the recognition of a key oncogenic driver ...

Journal: :The New England Journal of Medicine 2021

Hairy-cell leukemia (HCL) is a CD20+ indolent B-cell cancer in which BRAF V600E kinase–activating mutation plays pathogenetic role. In clinical trials involving patients with refractory or relapsed HCL, the targeting of oral inhibitor vemurafenib led to response 91% patients; 35% had complete response. However, median relapse-free survival was only 9 months after treatment stopped.

Journal: :Blood 2013
Mark L Heaney

In this issue of Blood, Haroche and colleagues report significant therapeutic activity of the BRAF inhibitor, vemurafenib, in 3 patients with rare histiocytic conditions, Erdheim-Chester disease and Langerhans cell histiocytosis.

Journal: :Cancers 2021

Melanoma is the deadliest form of skin cancer, primarily due to its high metastatic propensity and therapeutic resistance in advanced stages. The frequent inactivation p53 tumour suppressor protein melanomagenesis may predict promising outcomes for activators melanoma therapy. Herein, we aimed investigate antitumor potential p53-activating agent SLMP53-2 against melanoma. Two- three-dimensional...

2018
Manali Phadke Lily L. Remsing Rix Inna Smalley Annamarie T. Bryant Yunting Luo Harshani R. Lawrence Braydon J. Schaible Yian A. Chen Uwe Rix Keiran S. M. Smalley

Although the BRAF inhibitors dabrafenib and vemurafenib have both proven successful against BRAF-mutant melanoma, there seem to be differences in their mechanisms of action. Here, we show that dabrafenib is more effective at inhibiting the growth of NRAS-mutant and KRAS-mutant cancer cell lines than vemurafenib. Using mass spectrometry-based chemical proteomics, we identified NEK9 and CDK16 as ...

2015
Pramudita R. Prasetyanti Emily Capone Daniela Barcaroli Daniela D'Agostino Silvia Volpe Antonina Benfante Sander van Hooff Valentina Iacobelli Cosmo Rossi Stefano Iacobelli Jan Paul Medema Vincenzo De Laurenzi Gianluca Sala

Approximately 5-10% of metastatic colorectal cancers harbor a BRAF-V600E mutation, which is correlated with resistance to EGFR-targeted therapies and worse clinical outcome. Vice versa, targeted inhibition of BRAF-V600E with the selective inhibitor PLX 4032 (Vemurafenib) is severely limited due to feedback re-activation of EGFR in these tumors. Mounting evidence indicates that upregulation of t...

2015
Philipp Euskirchen Julien Haroche Jean-François Emile Ralph Buchert Staffan Vandersee Andreas Meisel

OBJECTIVE To describe a patient with life-threatening brainstem neurohistiocytosis who recovered completely upon targeted treatment with the V600E mutation-specific BRAF inhibitor vemurafenib. METHODS We report clinical, histiologic, genetic, and sequential imaging findings, including fluorodeoxyglucose (FDG)-PET, over a follow-up period of 11 months. RESULTS The patient presented with cent...

Journal: :Cancer discovery 2013
Matthew A Held Casey G Langdon James T Platt Tisheeka Graham-Steed Zongzhi Liu Ashok Chakraborty Antonella Bacchiocchi Andrew Koo Jonathan W Haskins Marcus W Bosenberg David F Stern

UNLABELLED Resistance and partial responses to targeted monotherapy are major obstacles in cancer treatment. Systematic approaches to identify efficacious drug combinations for cancer are not well established, especially in the context of genotype. To address this, we have tested pairwise combinations of an array of small-molecule inhibitors on early-passage melanoma cultures using combinatoria...

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