Targeting the IRE1α/XBP1 Endoplasmic Reticulum Stress Response Pathway in ARID1A-Mutant Ovarian Cancers

Joseph A Zundell1,2, Takeshi Fukumoto1, Jianhuang Lin1

  • 1Immunology, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, Pennsylvania.

Cancer Research
|September 22, 2021
PubMed

Insights

ARID1A mutations in ovarian cancer create a vulnerability in the endoplasmic reticulum stress response. Inhibiting the IRE1α-XBP1 pathway offers a promising therapeutic strategy for ARID1A-mutant ovarian clear cell carcinomas.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Genetics

Background:

  • SWI/SNF chromatin-remodeling complex alterations are common in human cancers.
  • ARID1A mutations are prevalent in ovarian clear cell carcinomas (OCCC), a cancer lacking effective treatments.

Purpose of the Study:

  • To investigate the role of ARID1A in the endoplasmic reticulum (ER) stress response.
  • To identify therapeutic targets for ARID1A-mutant OCCC.

Main Methods:

  • Investigated the transcriptional repression of the IRE1α-XBP1 axis by ARID1A.
  • Utilized genetic mouse models (conditional Arid1a knockout) and xenograft models (orthotopic and patient-derived).
  • Tested the efficacy of the IRE1α inhibitor B-I09, alone and in combination with HDAC6 inhibition.

Main Results:

  • ARID1A transcriptionally represses the IRE1α-XBP1 axis, conferring sensitivity to its inhibition.
  • ARID1A mutational status correlated with treatment response.
  • XBP1 knockout improved survival in a genetic mouse model of OCCC.
  • B-I09 suppressed tumor growth in vivo across multiple models.
  • B-I09 showed synergistic effects with HDAC6 inhibition.

Conclusions:

  • The IRE1α-XBP1 axis is a targetable vulnerability in ARID1A-mutant OCCC.
  • Pharmacological inhibition of IRE1α-XBP1, alone or with HDAC6 inhibitors, is a promising therapeutic strategy for ARID1A-mutant ovarian cancers.

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