E74-Like Factor 3 Is a Key Regulator of Epithelial Integrity and Immune Response Genes in Biliary Tract Cancer

Masami Suzuki, Mihoko Saito-Adachi, Yasuhito Arai, Yuko Fujiwara, Erina Takai, Shinsuke Shibata, Masahide Seki, Hirofumi Rokutan, Daichi Maeda, Masafumi Horie, Yutaka Suzuki, Tatsuhiro Shibata, Tohru Kiyono, Shinichi Yachida

Research output: Contribution to journalArticlepeer-review

Abstract

The transcription factor E74-like factor 3 (ELF3) is inactivated in a range of cancers, including biliary tract cancer (BTC). Here, we investigated the tumor-suppressive role of ELF3 in bile duct cells by identifying several previously unknown direct target genes of ELF3 that appear to be implicated in biliary duct carcinogenesis. ELF3 directly repressed ZEB2, a key regulator of epithelial–mesenchymal transition, and upregulated the expression of CGN, an integral element in lumen formation. Loss of ELF3 led to decreased cell–cell junctions and enhanced cell motility. ALOX5 and CXCL16 were also identified as additional direct targets of ELF3; their corresponding proteins 5-lipox-ygenase and CXCL16 play a role in the immune response. Conditioned medium from cells overexpressing ELF3 significantly enhanced the migration of natural killer cells and CD8þ T cells toward the conditioned medium. Gene expression profiling for BTC expressing high levels of ELF3 revealed significant enrichment of the ELF3-related genes. In a BTC xenograft model, activation of ELF3 increased expression of ELF3-related genes, enhanced the tubular structure of the tumors, and led to a loss of vimentin. Overall, our results indicate that ELF3 is a key regulator of both epithelial integrity and immune responses in BTC. Significance: Thease finding shows that ELF3 regulates epithelial integrity and host immune responses and functions as a tumor suppressor in biliary tract cancer.

Original languageEnglish
Pages (from-to)489-500
Number of pages12
JournalCancer Research
Volume81
Issue number2
DOIs
Publication statusPublished - 2021 Jan 15

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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