Cellular density-dependent down-regulation of EP4 prostanoid receptors via the up-regulation of hypoxia-inducible factor-1α in HCA-7 human colon cancer cells

Sho Otake, Kenji Yoshida, Naofumi Seira, Christopher M. Sanchez, John W Regan, Hiromichi Fujino, Toshihiko Murayama

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Increases in prostaglandin E2 (PGE2) and cyclooxygenase-2 (COX-2) levels are features of colon cancer. Among the different E-type prostanoid receptor subtypes, EP4 receptors are considered to play a crucial role in carcinogenesis by, for example, inducing COX-2 when stimulated with PGE2. However, EP4 receptor levels and PGE2-induced cellular responses are inconsistent among the cellular conditions. Therefore, the connections responsible for the expression of EP4 receptors were investigated in the present study by focusing on cell density-induced hypoxia-inducible factor-1α (HIF-1α). The expression of EP4 receptors was examined using immunoblot analysis, quantitative polymerase chain reaction, and reporter gene assays in HCA-7 human colon cancer cells with different cellular densities. The involvement of HIF-1α and its signaling pathways were also examined by immunoblot analysis, reporter gene assays, and with siRNA. We here demonstrated that EP4 receptors as well as EP4 receptor-mediated COX-2 expression levels decreased with an increase in cellular density. In contrast, HIF-1α levels increased in a cellular density-dependent manner. The knockdown of HIF-1α by siRNA restored the expression of EP4 receptors and EP4 receptor-mediated COX-2 in cells at a high density. Thus, the cellular density-dependent increase observed in HIF-1α expression levels reduced the expression of COX-2 by decreasing EP4 receptor levels. This novel regulation mechanism for the expression of EP4 receptors by HIF-1α may provide an explanation for the inconsistent actions of PGE2. The expression levels of EP4 receptors may vary depending on cellular density, which may lead to the differential activation of their signaling pathways by PGE2. Thus, cellular density-dependent PGE2-mediated signaling may determine the fate/stage of cancer cells, i.e., the surrounding environments could define the fate/stage of malignancies associated with colon cancer.

Original languageEnglish (US)
Pages (from-to)1-13
Number of pages13
JournalPharmacology Research and Perspectives
Volume3
Issue number1
DOIs
StatePublished - Feb 1 2015

Fingerprint

Hypoxia-Inducible Factor 1
Dinoprostone
Colonic Neoplasms
Prostaglandins
Cyclooxygenase 2
Up-Regulation
Down-Regulation
Reporter Genes
Small Interfering RNA
Receptors, Prostaglandin E, EP4 Subtype
Prostaglandin-Endoperoxide Synthases
Neoplasms
Carcinogenesis
Cell Count
Polymerase Chain Reaction

Keywords

  • PGE
  • Cell density
  • COX-2
  • EP4 prostanoid receptor
  • GPCRs
  • HCA-7 cells
  • HIF-1α
  • Human colon cancer

ASJC Scopus subject areas

  • Pharmacology, Toxicology and Pharmaceutics(all)
  • Neurology

Cite this

Cellular density-dependent down-regulation of EP4 prostanoid receptors via the up-regulation of hypoxia-inducible factor-1α in HCA-7 human colon cancer cells. / Otake, Sho; Yoshida, Kenji; Seira, Naofumi; Sanchez, Christopher M.; Regan, John W; Fujino, Hiromichi; Murayama, Toshihiko.

In: Pharmacology Research and Perspectives, Vol. 3, No. 1, 01.02.2015, p. 1-13.

Research output: Contribution to journalArticle

Otake, Sho ; Yoshida, Kenji ; Seira, Naofumi ; Sanchez, Christopher M. ; Regan, John W ; Fujino, Hiromichi ; Murayama, Toshihiko. / Cellular density-dependent down-regulation of EP4 prostanoid receptors via the up-regulation of hypoxia-inducible factor-1α in HCA-7 human colon cancer cells. In: Pharmacology Research and Perspectives. 2015 ; Vol. 3, No. 1. pp. 1-13.
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