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Targeting the IRE1α/XBP1s pathway suppresses CARM1-expressing ovarian cancer

CARM1 is often overexpressed in human cancers including in ovarian cancer. However, therapeutic approaches based on CARM1 expression remain to be an unmet need. Cancer cells exploit adaptive responses such as the endoplasmic reticulum (ER) stress response for their survival through activating pathwa...

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Detalles Bibliográficos
Autores principales: Lin, Jianhuang, Liu, Heng, Fukumoto, Takeshi, Zundell, Joseph, Yan, Qingqing, Tang, Chih-Hang Anthony, Wu, Shuai, Zhou, Wei, Guo, Dajiang, Karakashev, Sergey, Hu, Chih-Chi Andrew, Sarma, Kavitha, Kossenkov, Andrew V., Zhang, Rugang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8423755/
https://www.ncbi.nlm.nih.gov/pubmed/34493732
http://dx.doi.org/10.1038/s41467-021-25684-3
Descripción
Sumario:CARM1 is often overexpressed in human cancers including in ovarian cancer. However, therapeutic approaches based on CARM1 expression remain to be an unmet need. Cancer cells exploit adaptive responses such as the endoplasmic reticulum (ER) stress response for their survival through activating pathways such as the IRE1α/XBP1s pathway. Here, we report that CARM1-expressing ovarian cancer cells are selectively sensitive to inhibition of the IRE1α/XBP1s pathway. CARM1 regulates XBP1s target gene expression and directly interacts with XBP1s during ER stress response. Inhibition of the IRE1α/XBP1s pathway was effective against ovarian cancer in a CARM1-dependent manner both in vitro and in vivo in orthotopic and patient-derived xenograft models. In addition, IRE1α inhibitor B-I09 synergizes with immune checkpoint blockade anti-PD1 antibody in an immunocompetent CARM1-expressing ovarian cancer model. Our data show that pharmacological inhibition of the IRE1α/XBP1s pathway alone or in combination with immune checkpoint blockade represents a therapeutic strategy for CARM1-expressing cancers.