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ID 115684
Author
Seira, Naofumi Chiba University
Yamagata, Kazuyuki Chiba University
Araki, Yumi Chiba University|Tokushima University
Kurata, Naoki Chiba University|Tokushima University
Yanagisawa, Naoki Chiba University
Mashimo, Masato Doshisha Women's College of Liberal Arts
Nakamura, Hiroyuki Chiba University
Regan, John W. The University of Arizona
Murayama, Toshihiko Chiba University
Keywords
c-Myc
colorectal cancer
EP4 receptors
HIF-1α
homeostasis
Sp-1
Content Type
Journal Article
Description
The up‐regulated expression of E‐type prostanoid (EP) 4 receptors has been implicated in carcinogenesis; however, the expression of EP4 receptors has also been reported to be weaker in tumor tissues than in normal tissues. Indeed, EP4 receptors have been suggested to play a role in the maintenance of colorectal homeostasis. This study aimed to examine the underlying mechanisms/reasons for why inconsistent findings have been reported regarding EP4 receptor expression levels in homeostasis and carcinogenesis by focusing on cellular densities. Thus, the human colon cancer HCA‐7 cells, which retain some functional features of normal epithelia, and luciferase reporter genes containing wild‐type or mutated EP4 receptor promoters were used for elucidating the cellular density‐dependent mechanisms about the regulation of EP4 receptor expression. In silico analysis was also utilized for confirming the relevance of the findings with respect to colon cancer development. We here demonstrated that the expression of EP4 receptors was up‐regulated by c‐Myc by binding to Sp‐1 under low cellular density conditions, but was down‐regulated under high cellular density conditions via the increase in the expression levels of HIF‐1α protein, which may pull out c‐Myc and Sp‐1 from DNA‐binding. The tightly regulated EP4 receptor expression mechanism may be a critical system for maintaining homeostasis in normal colorectal epithelial cells. Therefore, once the system is altered, possibly due to the transient overexpression of EP4 receptors, it may result in aberrant cellular proliferation and transformation to cancerous phenotypes. However, at the point, EP4 receptors themselves and their mediated homeostasis would be no longer required.
Journal Title
Pharmacology Research & Perspectives
ISSN
20521707
Publisher
John Wiley & Sons|British Pharmacological Society|American Society for Pharmacology and Experimental Therapeutics
Volume
6
Issue
6
Start Page
e00441
Published Date
2018-11-11
Rights
This is an open access article under the terms of the Creative Commons Attribution License(https://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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DOI (Published Version)
URL ( Publisher's Version )
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language
eng
TextVersion
Publisher
departments
Pharmaceutical Sciences