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Alterations in Gene Expression of Renin-Angiotensin System Components and Related Proteins in Colorectal Cancer
Author(s) -
Danial Mehranfard,
Gabriela Pérez,
Andrés Rodríguez,
Julia Ladna,
Christopher T. Neagra,
Benjamin I. Goldstein,
Timothy Carroll,
Alice Tran,
Malav Trivedi,
Robert C. Speth
Publication year - 2021
Publication title -
journal of the renin-angiotensin-aldosterone system
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.457
H-Index - 46
eISSN - 1752-8976
pISSN - 1470-3203
DOI - 10.1155/2021/9987115
Subject(s) - neprilysin , downregulation and upregulation , renin–angiotensin system , gene expression , biology , gene , cancer research , aminopeptidase , enzyme , endocrinology , genetics , biochemistry , amino acid , leucine , blood pressure
Materials and Methods Quantitative expression of the RNA of these 17 genes in normal and cancerous tissues obtained using chip arrays from the public functional genomics data repository, Gene Expression Omnibus (GEO) application, was compared statistically.Results Expression of four genes, AGT (angiotensinogen), ENPEP (aminopeptidase A) MME (neprilysin), and PREP (prolyl endopeptidase), was significantly upregulated in CRC specimens. Expression of REN (renin), THOP (thimet oligopeptidase), NLN (neurolysin), PRCP (prolyl carboxypeptidase), ANPEP (aminopeptidase N), and MAS1 (Mas receptor) was downregulated in CRC specimens.Conclusions Presuming gene expression parallel protein expression, these results suggest that increased production of the angiotensinogen precursor of angiotensin (ANG) peptides, with the reduction of the enzymes that metabolize it to ANG II, can lead to accumulation of angiotensinogen in CRC tissues. Downregulation of THOP , NLN , PRCP , and MAS1 gene expression, whose proteins contribute to the ACE2/ANG 1-7/Mas axis, suggests that reduced activity of this RAS branch could be permissive for oncogenicity. Components of the RAS may be potential therapeutic targets for treatment of CRC.

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