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The lincRNA MIRAT binds to IQGAP1 and modulates the MAPK pathway in NRAS mutant melanoma.
Sanlorenzo, Martina; Vujic, Igor; Esteve-Puig, Rosaura; Lai, Kevin; Vujic, Marin; Lin, Kevin; Posch, Christian; Dimon, Michelle; Moy, Adrian; Zekhtser, Mitchell; Johnston, Katia; Gho, Deborah; Ho, Wilson; Gajjala, Abhinay; Oses Prieto, Juan; Burlingame, Alma; Daud, Adil; Rappersberger, Klemens; Ortiz-Urda, Susana.
Afiliação
  • Sanlorenzo M; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
  • Vujic I; Department of Oncology, University of Turin, Torino, 10124, Italy.
  • Esteve-Puig R; Institute of Cancer Research, Department of Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, 1090, Austria.
  • Lai K; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
  • Vujic M; The Rudolfstiftung Hospital, Department of Dermatology, Vienna, 1030, Austria.
  • Lin K; School of Medicine, Sigmund Freud University Vienna, Vienna, 1020, Austria.
  • Posch C; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
  • Dimon M; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
  • Moy A; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
  • Zekhtser M; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
  • Johnston K; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
  • Gho D; The Rudolfstiftung Hospital, Department of Dermatology, Vienna, 1030, Austria.
  • Ho W; School of Medicine, Sigmund Freud University Vienna, Vienna, 1020, Austria.
  • Gajjala A; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
  • Oses Prieto J; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
  • Burlingame A; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
  • Daud A; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
  • Rappersberger K; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
  • Ortiz-Urda S; University of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
Sci Rep ; 8(1): 10902, 2018 Jul 19.
Article em En | MEDLINE | ID: mdl-30026510
ABSTRACT
Despite major advances in targeted melanoma therapies, drug resistance limits their efficacy. Long noncoding RNAs (lncRNAs) are transcriptome elements that do not encode proteins but are important regulatory molecules. LncRNAs have been implicated in cancer development and response to different therapeutics and are thus potential treatment targets; however, the majority of their functions and molecular interactions remain unexplored. In this study, we identify a novel cytoplasmic intergenic lincRNA (MIRAT), which is upregulated following prolonged MAPK inhibition in NRAS mutant melanoma and modulates MAPK signaling by binding to the MEK scaffold protein IQGAP1. Collectively, our results present MIRAT's direct modulatory effect on the MAPK pathway and highlight the relevance of cytoplasmic lncRNAs as potential targets in drug resistant cancer.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Resistencia a Medicamentos Antineoplásicos / Proteínas Ativadoras de ras GTPase / RNA Longo não Codificante / GTP Fosfo-Hidrolases / Melanoma / Proteínas de Membrana / Mutação Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Resistencia a Medicamentos Antineoplásicos / Proteínas Ativadoras de ras GTPase / RNA Longo não Codificante / GTP Fosfo-Hidrolases / Melanoma / Proteínas de Membrana / Mutação Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article