Super-Enhancer-Associated LncRNA UCA1 Interacts Directly with AMOT to Activate YAP Target Genes in Epithelial Ovarian Cancer

Xianzhi Lin; Tassja J. Spindler; Marcos Abraão de Souza Fonseca; Rosario I. Corona; Ji-Heui Seo; Felipe Segato Dezem; Lewyn Li; Janet M. Lee; Henry W. Long; Thomas A. Sellers; Beth Y. Karlan; Houtan Noushmehr; Matthew L. Freedman; Simon A. Gayther; Kate Lawrenson

iScience (Jul 2019)

Super-Enhancer-Associated LncRNA UCA1 Interacts Directly with AMOT to Activate YAP Target Genes in Epithelial Ovarian Cancer

Xianzhi Lin,
Tassja J. Spindler,
Marcos Abraão de Souza Fonseca,
Rosario I. Corona,
Ji-Heui Seo,
Felipe Segato Dezem,
Lewyn Li,
Janet M. Lee,
Henry W. Long,
Thomas A. Sellers,
Beth Y. Karlan,
Houtan Noushmehr,
Matthew L. Freedman,
Simon A. Gayther,
Kate Lawrenson

Affiliations

Xianzhi Lin: Women's Cancer Program at the Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA
Tassja J. Spindler: Women's Cancer Program at the Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA
Marcos Abraão de Souza Fonseca: Department of Genetics, University of Sao Paulo, Ribeirao Preto, Sao Paulo, Brazil
Rosario I. Corona: Women's Cancer Program at the Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA; Center for Bioinformatics and Functional Genomics, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA
Ji-Heui Seo: Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA
Felipe Segato Dezem: Department of Genetics, University of Sao Paulo, Ribeirao Preto, Sao Paulo, Brazil
Lewyn Li: Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA
Janet M. Lee: Center for Bioinformatics and Functional Genomics, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA
Henry W. Long: Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA; Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, MA, USA
Thomas A. Sellers: Department of Cancer Epidemiology, Moffitt Cancer Center, Tampa, FL, USA
Beth Y. Karlan: Women's Cancer Program at the Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA
Houtan Noushmehr: Department of Genetics, University of Sao Paulo, Ribeirao Preto, Sao Paulo, Brazil; Department of Neurosurgery, Henry Ford Health System, Detroit, MI, USA
Matthew L. Freedman: Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA; Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, MA, USA; The Eli and Edythe L. Broad Institute, Cambridge, MA, USA
Simon A. Gayther: Center for Bioinformatics and Functional Genomics, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA
Kate Lawrenson: Women's Cancer Program at the Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA; Center for Bioinformatics and Functional Genomics, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA; Corresponding author

Journal volume & issue: Vol. 17
pp. 242 – 255

Abstract

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Summary: Long noncoding RNAs (lncRNAs) have emerged as critical regulators of tumorigenesis, and yet their mechanistic roles remain challenging to characterize. Here, we integrate functional proteomics with lncRNA-interactome profiling to characterize Urothelial Cancer Associated 1 (UCA1), a candidate driver of ovarian cancer development. Reverse phase protein array (RPPA) analysis indicates that UCA1 activates transcription coactivator YAP and its target genes. In vivo RNA antisense purification (iRAP) of UCA1 interacting proteins identified angiomotin (AMOT), a known YAP regulator, as a direct binding partner. Loss-of-function experiments show that AMOT mediates YAP activation by UCA1, as UCA1 enhances the AMOT-YAP interaction to promote YAP dephosphorylation and nuclear translocation. Together, we characterize UCA1 as a lncRNA regulator of Hippo-YAP signaling and highlight the UCA1-AMOT-YAP signaling axis in ovarian cancer development. : Cancer Systems Biology; Omics; Proteomics; Systems Biology Subject Areas: Cancer Systems Biology, Omics, Proteomics, Systems Biology

Published in iScience

ISSN: 2589-0042 (Online)
Publisher: Elsevier
Country of publisher: United States
LCC subjects: Science
Website: http://www.cell.com/iscience/home

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