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Induction of cell differentiation activates transcription of the Sarco/Endoplasmic Reticulum calcium‐ATPase 3 gene ( ATP2A3 ) in gastric and colon cancer cells
Author(s) -
FloresPeredo Lucía,
Rodríguez Gabriela,
ZarainHerzberg Angel
Publication year - 2017
Publication title -
molecular carcinogenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.254
H-Index - 97
eISSN - 1098-2744
pISSN - 0899-1987
DOI - 10.1002/mc.22529
Subject(s) - biology , endoplasmic reticulum , microbiology and biotechnology , cellular differentiation , transcription factor , carcinogenesis , transfection , cancer cell , cell culture , gene , cancer , genetics
The Sarco/Endoplasmic Reticulum Ca 2+ ‐ATPases (SERCAs), pump Ca 2+ into the endoplasmic reticulum lumen modulating cytosolic Ca 2+ concentrations to regulate various cellular processes including cell growth. Previous studies have reported a downregulation of SERCA3 protein expression in gastric and colon cancer cell lines and showed that in vitro cell differentiation increases its expression. However, little is known about the transcriptional mechanisms and transcription factors that regulate SERCA3 expression in epithelial cancer cells. In this work, we demonstrate that SERCA3 mRNA is upregulated up to 45‐fold in two epithelial cancer cell lines, KATO‐III and Caco‐2, induced to differentiate with histone deacetylase inhibitors (HDACi) and by cell confluence, respectively. To evaluate the transcriptional elements responding to the differentiation stimuli, we cloned the human ATP2A3 promoter, generated deletion constructs and transfected them into KATO‐III cells. Basal and differentiation responsive DNA elements were located by functional analysis within the first −135 bp of the promoter region. Using site‐directed mutagenesis and DNA‐protein binding assays we found that Sp1, Sp3, and Klf‐4 transcription factors bind to ATP2A3 proximal promoter elements and regulate basal gene expression. We showed that these factors participated in the increase of ATP2A3 expression during cancer cell differentiation. This study provides evidence for the first time that Sp1, Sp3, and Klf‐4 transcriptionally modulate the expression of SERCA3 during induction of epithelial cancer cell differentiation. © 2016 Wiley Periodicals, Inc.