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Characterization and significance of ACE2 and Mas receptor in human colon adenocarcinoma.

BERNARDI, STELLA
•
ZENNARO, CRISTINA
•
PALMISANO, SILVIA
altro
FABRIS, BRUNO
2012
  • journal article

Periodico
JRAAS
Abstract
NTRODUCTION: A new arm of the renin-angiotensin system (RAS) has been recently characterized; this includes angiotensin converting enzyme (ACE)2 and angiotensin (Ang)1-7, a heptapeptide acting through the Mas receptor (MasR). Recent studies show that Ang1-7 has an antiproliferative action on lung adenocarcinoma cells. The aim of this study was to characterize RAS expression in human colon adenocarcinoma and to investigate whether Ang1-7 exerts an antiproliferative effect on human colon adenocarcinoma cells. MATERIALS AND METHODS: Gene, protein expression and enzymatic activity of the main components of the RAS were determined on non-neoplastic colon mucosa as well as on the tumor mass and the mucosa taken 5 cm distant from it, both collected from patients with colon adenocarcinoma. Two different human colon cancer cell lines were treated with AngII and Ang1-7. RESULTS: The novel finding of this study was that MasR was significantly upregulated in colon adenocarcinoma compared with non-neoplastic colon mucosa, which showed little or no expression of it. ACE gene expression and enzymatic activity were also increased in the tumors. However, AngII and Ang1-7 did not have any pro-/antiproliferative effects in the cell lines studied. CONCLUSIONS: The data suggest that upregulation of the MasR could be used as a diagnostic marker of colon adenocarcinoma.
DOI
10.1177/1470320311426023
WOS
WOS:000300993400026
Archivio
http://hdl.handle.net/11368/2494552
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84859993289
Diritti
metadata only access
Soggetti
  • Angiotensin convertin...

  • angiotensin 1-7

  • cell cycle

  • cell line

  • colon adenocarcinoma

  • Mas receptor

  • oncogene

  • renin–angiotensin sys...

Scopus© citazioni
38
Data di acquisizione
Jun 15, 2022
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Web of Science© citazioni
43
Data di acquisizione
Mar 26, 2024
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Data di acquisizione
Apr 19, 2024
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