Literature DB >> 28543700

Interaction of molecular alterations with immune response in melanoma.

Robert A Szczepaniak Sloane1, Vancheswaran Gopalakrishnan1, Sangeetha M Reddy2, Xue Zhang1, Alexandre Reuben1, Jennifer A Wargo1,3.   

Abstract

Major advances have been made in melanoma treatment with the use of molecularly targeted therapies and immunotherapies, and numerous regimens are now approved by the US Food and Drug Administration for patients with stage IV disease. However, therapeutic resistance remains an issue to both classes of agents, and reliable biomarkers of therapeutic response and resistance are lacking. Mechanistic insights are being gained through preclinical studies and translational research, offering potential strategies to enhance responses and survival in treated patients. A comprehensive understanding of the immune effects of common mutations at play in melanoma is critical, as is an appreciation of the molecular mechanisms contributing to therapeutic resistance to immunotherapy. These mechanisms and the interplay between them are discussed herein. Cancer 2017;123:2130-42.
© 2017 American Cancer Society. © 2017 American Cancer Society.

Entities:  

Keywords:  B-Raf proto-oncogene serine/threonine kinase (BRAF); catenin-β 1 (CTNNB1); combination therapy; guanosine-triphosphate guanyltransferase (GTPase); immunotherapy; melanoma; neoantigen; neuroblastoma rat sarcoma viral oncogene homolog (NRAS); personalized medicine; phosphatase and tensin homolog (PTEN); targeted therapy

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Year:  2017        PMID: 28543700      PMCID: PMC6105277          DOI: 10.1002/cncr.30681

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  102 in total

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3.  In melanoma, RAS mutations are accompanied by switching signaling from BRAF to CRAF and disrupted cyclic AMP signaling.

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Review 4.  Adaptive clinical trial design.

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5.  Mice with Pulmonary Fibrosis Driven by Telomere Dysfunction.

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Journal:  Cell Rep       Date:  2015-07-02       Impact factor: 9.423

6.  Screening of N-ras codon 61 mutations in paired primary and metastatic cutaneous melanomas: mutations occur early and persist throughout tumor progression.

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7.  Selective BRAFV600E inhibition enhances T-cell recognition of melanoma without affecting lymphocyte function.

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Journal:  Cancer Res       Date:  2010-06-15       Impact factor: 12.701

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10.  Phase II study of vemurafenib followed by ipilimumab in patients with previously untreated BRAF-mutated metastatic melanoma.

Authors:  Asim Amin; David H Lawson; April K S Salama; Henry B Koon; Troy Guthrie; Sajeve S Thomas; Steven J O'Day; Montaser F Shaheen; Bin Zhang; Stephen Francis; F Stephen Hodi
Journal:  J Immunother Cancer       Date:  2016-08-16       Impact factor: 13.751

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  10 in total

Review 1.  Rho GTPase effectors and NAD metabolism in cancer immune suppression.

Authors:  Mahmoud Chaker; Audrey Minden; Suzie Chen; Robert H Weiss; Eduardo N Chini; Amit Mahipal; Asfar S Azmi
Journal:  Expert Opin Ther Targets       Date:  2017-12-10       Impact factor: 6.902

Review 2.  Melanoma and Immune Checkpoint Inhibitors.

Authors:  Masutaka Furue; Takamichi Ito; Naoko Wada; Maiko Wada; Takafumi Kadono; Hiroshi Uchi
Journal:  Curr Oncol Rep       Date:  2018-03-23       Impact factor: 5.075

3.  Cancer: Precision T-cell therapy targets tumours.

Authors:  Cornelis J M Melief
Journal:  Nature       Date:  2017-07-05       Impact factor: 49.962

Review 4.  Cancer immunotherapy with immunoadjuvants, nanoparticles, and checkpoint inhibitors: Recent progress and challenges in treatment and tracking response to immunotherapy.

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Journal:  Pharmacol Ther       Date:  2019-12-19       Impact factor: 12.310

5.  B4GALNT1 induces angiogenesis, anchorage independence growth and motility, and promotes tumorigenesis in melanoma by induction of ganglioside GM2/GD2.

Authors:  Hideki Yoshida; Lisa Koodie; Kari Jacobsen; Ken Hanzawa; Yasuhide Miyamoto; Masato Yamamoto
Journal:  Sci Rep       Date:  2020-01-27       Impact factor: 4.379

6.  Immune signature as predictive marker for response to checkpoint inhibitor immunotherapy and overall survival in melanoma.

Authors:  Franziska K Krebs; Emily R Trzeciak; Sophia Zimmer; Deniz Özistanbullu; Heidrun Mitzel-Rink; Markus Meissner; Stephan Grabbe; Carmen Loquai; Andrea Tuettenberg
Journal:  Cancer Med       Date:  2021-01-15       Impact factor: 4.452

7.  Association of NRAS Mutation With Clinical Outcomes of Anti-PD-1 Monotherapy in Advanced Melanoma: A Pooled Analysis of Four Asian Clinical Trials.

Authors:  Li Zhou; Xuan Wang; Zhihong Chi; Xinan Sheng; Yan Kong; Lili Mao; Bin Lian; Bixia Tang; Xieqiao Yan; Xue Bai; Siming Li; Jun Guo; Chuanliang Cui; Lu Si
Journal:  Front Immunol       Date:  2021-07-05       Impact factor: 7.561

8.  Salvage pembrolizumab added to kinase inhibitor therapy for the treatment of anaplastic thyroid carcinoma.

Authors:  Priyanka C Iyer; Ramona Dadu; Maria Gule-Monroe; Naifa L Busaidy; Renata Ferrarotto; Mouhammed Amir Habra; Mark Zafereo; Michelle D Williams; G Brandon Gunn; Horiana Grosu; Heath D Skinner; Erich M Sturgis; Neil Gross; Maria E Cabanillas
Journal:  J Immunother Cancer       Date:  2018-07-11       Impact factor: 13.751

9.  Identification of high-dimensional omics-derived predictors for tumor growth dynamics using machine learning and pharmacometric modeling.

Authors:  Laura B Zwep; Kevin L W Duisters; Martijn Jansen; Tingjie Guo; Jacqueline J Meulman; Parth J Upadhyay; J G Coen van Hasselt
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2021-04-08

10.  Combination of Lenvatinib and Pembrolizumab as Salvage Treatment for Paucicellular Variant of Anaplastic Thyroid Cancer: A Case Report.

Authors:  Cristina Luongo; Tommaso Porcelli; Francesca Sessa; Maria Angela De Stefano; Francesco Scavuzzo; Vincenzo Damiano; Michele Klain; Claudio Bellevicine; Elide Matano; Giancarlo Troncone; Martin Schlumberger; Domenico Salvatore
Journal:  Curr Oncol       Date:  2021-12-16       Impact factor: 3.677

  10 in total

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