Literature DB >> 19464601

BRAF signaling and targeted therapies in melanoma.

Nathalie Dhomen1, Richard Marais.   

Abstract

The RAS/RAF/MEK/ERK signaling pathway has emerged as a major player in the induction and maintenance of melanoma, particularly the protein kinase BRAF, mutated in approximately 44% of melanoma cases. The availability of new drugs affecting the components of this pathway and pathways that may cooperate with MAPK signaling, means that targeted therapies are fast becoming a real option in the clinical management of melanoma. The authors discuss what they learned from clinical trials using first- and second-generation inhibitors to this pathway.

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Year:  2009        PMID: 19464601     DOI: 10.1016/j.hoc.2009.04.001

Source DB:  PubMed          Journal:  Hematol Oncol Clin North Am        ISSN: 0889-8588            Impact factor:   3.722


  68 in total

Review 1.  Targeting the MAPK pathway in melanoma: why some approaches succeed and other fail.

Authors:  Gajanan S Inamdar; SubbaRao V Madhunapantula; Gavin P Robertson
Journal:  Biochem Pharmacol       Date:  2010-05-09       Impact factor: 5.858

2.  Oncogenic BRAF induces chronic ER stress condition resulting in increased basal autophagy and apoptotic resistance of cutaneous melanoma.

Authors:  M Corazzari; F Rapino; F Ciccosanti; P Giglio; M Antonioli; B Conti; G M Fimia; P E Lovat; M Piacentini
Journal:  Cell Death Differ       Date:  2014-11-07       Impact factor: 15.828

Review 3.  Dormancy of metastatic melanoma.

Authors:  Liliana Ossowski; Julio A Aguirre-Ghiso
Journal:  Pigment Cell Melanoma Res       Date:  2009-10-19       Impact factor: 4.693

Review 4.  BRAF in malignant melanoma progression and metastasis: potentials and challenges.

Authors:  Aljawharah Alqathama
Journal:  Am J Cancer Res       Date:  2020-04-01       Impact factor: 6.166

5.  The potential for BRAF V600 inhibitors in advanced cutaneous melanoma: rationale and latest evidence.

Authors:  Charlotte Lemech; Jeffrey Infante; Hendrik-Tobias Arkenau
Journal:  Ther Adv Med Oncol       Date:  2012-03       Impact factor: 8.168

6.  Inoperable bulky melanoma responds to neoadjuvant therapy with vemurafenib.

Authors:  Niloofar Fadaki; Servando Cardona-Huerta; Lea Martineau; Suresh Thummala; Shih-Tsung Cheng; Steve R Bunker; Richard Garcia-Kennedy; Wei Wang; David Minor; Mohammed Kashani-Sabet; Stanley P L Leong
Journal:  BMJ Case Rep       Date:  2012-10-22

Review 7.  Biology-driven cancer drug development: back to the future.

Authors:  Christopher J Lord; Alan Ashworth
Journal:  BMC Biol       Date:  2010-04-12       Impact factor: 7.431

8.  Melanoma: a model for testing new agents in combination therapies.

Authors:  Paolo A Ascierto; Howard Z Streicher; Mario Sznol
Journal:  J Transl Med       Date:  2010-04-20       Impact factor: 5.531

9.  PLX4032, a selective BRAF(V600E) kinase inhibitor, activates the ERK pathway and enhances cell migration and proliferation of BRAF melanoma cells.

Authors:  Ruth Halaban; Wengeng Zhang; Antonella Bacchiocchi; Elaine Cheng; Fabio Parisi; Stephan Ariyan; Michael Krauthammer; James P McCusker; Yuval Kluger; Mario Sznol
Journal:  Pigment Cell Melanoma Res       Date:  2010-02-10       Impact factor: 4.693

10.  Small molecule screening in zebrafish: an in vivo approach to identifying new chemical tools and drug leads.

Authors:  Kerrie L Taylor; Nicola J Grant; Nicholas D Temperley; E Elizabeth Patton
Journal:  Cell Commun Signal       Date:  2010-06-12       Impact factor: 5.712

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