Literature DB >> 27087480

The state of melanoma: challenges and opportunities.

Glenn Merlino1, Meenhard Herlyn2, David E Fisher3, Boris C Bastian4, Keith T Flaherty5, Michael A Davies6, Jennifer A Wargo6, Clara Curiel-Lewandrowski7, Michael J Weber8, Sancy A Leachman9, Maria S Soengas10, Martin McMahon11, J William Harbour12, Susan M Swetter13, Andrew E Aplin14, Michael B Atkins15, Marcus W Bosenberg16, Reinhard Dummer17, Jeffrey E Gershenwald6, Allan C Halpern18, Dorothee Herlyn2, Giorgos C Karakousis19, John M Kirkwood20, Michael Krauthammer21, Roger S Lo22, Georgina V Long23, Grant McArthur24, Antoni Ribas22, Lynn Schuchter19, Jeffrey A Sosman25, Keiran S Smalley26, Patricia Steeg27, Nancy E Thomas28, Hensin Tsao29, Thomas Tueting30, Ashani Weeraratna2, George Xu19, Randy Lomax31, Alison Martin31, Steve Silverstein31, Tim Turnham31, Ze'ev A Ronai32.   

Abstract

The Melanoma Research Foundation (MRF) has charted a comprehensive assessment of the current state of melanoma research and care. Intensive discussions among members of the MRF Scientific Advisory Council and Breakthrough Consortium, a group that included clinicians and scientists, focused on four thematic areas - diagnosis/early detection, prevention, tumor cell dormancy (including metastasis), and therapy (response and resistance). These discussions extended over the course of 2015 and culminated at the Society of Melanoma Research 2015 International Congress in November. Each of the four groups has outlined their thoughts as per the current status, challenges, and opportunities in the four respective areas. The current state and immediate and long-term needs of the melanoma field, from basic research to clinical management, are presented in the following report.
© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  dormancy; early diagnosis; melanoma; metastasis; prevention; therapy

Mesh:

Year:  2016        PMID: 27087480      PMCID: PMC5228487          DOI: 10.1111/pcmr.12475

Source DB:  PubMed          Journal:  Pigment Cell Melanoma Res        ISSN: 1755-1471            Impact factor:   4.693


  37 in total

1.  cAMP-independent non-pigmentary actions of variant melanocortin 1 receptor: AKT-mediated activation of protective responses to oxidative DNA damage.

Authors:  María Castejón-Griñán; Cecilia Herraiz; Conchi Olivares; Celia Jiménez-Cervantes; Jose Carlos García-Borrón
Journal:  Oncogene       Date:  2018-04-06       Impact factor: 9.867

2.  ErbB3 Targeting Enhances the Effects of MEK Inhibitor in Wild-Type BRAF/NRAS Melanoma.

Authors:  Claudia Capparelli; Timothy J Purwin; Shea A Heilman; Inna Chervoneva; Peter A McCue; Adam C Berger; Michael A Davies; Jeffrey E Gershenwald; Clemens Krepler; Andrew E Aplin
Journal:  Cancer Res       Date:  2018-08-16       Impact factor: 12.701

3.  H3K27me3-mediated PGC1α gene silencing promotes melanoma invasion through WNT5A and YAP.

Authors:  Chi Luo; Eduardo Balsa; Elizabeth A Perry; Jiaxin Liang; Clint D Tavares; Francisca Vazquez; Hans R Widlund; Pere Puigserver
Journal:  J Clin Invest       Date:  2020-02-03       Impact factor: 14.808

4.  Vemurafenib and trametinib reduce expression of CTGF and IL-8 in V600EBRAF melanoma cells.

Authors:  Mariusz L Hartman; Michal Rozanski; Marta Osrodek; Izabela Zalesna; Malgorzata Czyz
Journal:  Lab Invest       Date:  2017-01-09       Impact factor: 5.662

5.  Association of Time From Primary Diagnosis to First Distant Relapse of Metastatic Melanoma With Progression of Disease and Survival.

Authors:  Anaïs Vallet; Bastien Oriano; Laurent Mortier; Stéphane Dalle; Caroline Dutriaux; Bernard Guillot; Marie-Thérèse Leccia; Sophie Dalac; Philippe Saiag; Jean-Philippe Lacour; Delphine Legoupil; Julie De Quatrebarbes; Florence Brunet-Possenti; Thierry Lesimple; Jean-Philippe Arnault; François Aubin; Florence Granel-Brocard; Pierre-Emmanuel Stoebner; Eve Maubec; Brigitte Dreno; Clara Allayous; Raphaël Porcher; Céleste Lebbé
Journal:  JAMA Dermatol       Date:  2019-06-01       Impact factor: 10.282

6.  FREQUENT SUBCLINICAL MACULAR CHANGES IN COMBINED BRAF/MEK INHIBITION WITH HIGH-DOSE HYDROXYCHLOROQUINE AS TREATMENT FOR ADVANCED METASTATIC BRAF MUTANT MELANOMA: Preliminary Results From a Phase I/II Clinical Treatment Trial.

Authors:  Akosua A Nti; Leona W Serrano; Harpal S Sandhu; Katherine E Uyhazi; Ilaina D Edelstein; Elaine J Zhou; Scott Bowman; Delu Song; Tara C Gangadhar; Lynn M Schuchter; Sheryl Mitnick; Alexander Huang; Charles W Nichols; Ravi K Amaravadi; Benjamin J Kim; Tomas S Aleman
Journal:  Retina       Date:  2019-03       Impact factor: 4.256

Review 7.  The Role of Autophagy in the Resistance to BRAF Inhibition in BRAF-Mutated Melanoma.

Authors:  Xiao Liu; Jinfeng Wu; Haihong Qin; Jinhua Xu
Journal:  Target Oncol       Date:  2018-08       Impact factor: 4.493

8.  Hypoxia-induced HIF1α targets in melanocytes reveal a molecular profile associated with poor melanoma prognosis.

Authors:  Stacie K Loftus; Laura L Baxter; Julia C Cronin; Temesgen D Fufa; William J Pavan
Journal:  Pigment Cell Melanoma Res       Date:  2017-04-19       Impact factor: 4.693

Review 9.  Melanoma Brain Metastases: Current Areas of Investigation and Future Directions.

Authors:  Isabella Glitza Oliva; Hussein Tawbi; Michael A Davies
Journal:  Cancer J       Date:  2017 Jan/Feb       Impact factor: 3.360

10.  A Targeted Quantitative Proteomic Approach Assesses the Reprogramming of Small GTPases during Melanoma Metastasis.

Authors:  Ming Huang; Tianyu F Qi; Lin Li; Gao Zhang; Yinsheng Wang
Journal:  Cancer Res       Date:  2018-08-02       Impact factor: 12.701

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.