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Arginase is involved in cervical lesions progression and severity.

Authors :
Souid M
Ghedira R
Souissi S
Bouzgarrou N
Gabbouj S
Shini-Hadhri S
Rhim MS
Boukadida A
Toumi D
Faleh R
Bouaouina N
Zakhama A
Hassen E
Source :
Immunobiology [Immunobiology] 2022 Mar; Vol. 227 (2), pp. 152189. Date of Electronic Publication: 2022 Feb 16.
Publication Year :
2022

Abstract

Background: Little is known about the relationship between arginase, an immunosuppressive enzyme, and cervical lesions. The present study is aimed at evaluating arginase activity in plasma and mRNA arginase isoforms expression in cervical cells of patients with abnormal cytology and identifying their relationship with Human papillomavirus (HPV) related parameters such as: HPV type, HPV circulating viral load and anti-HPV16 IgG.<br />Methods: This study included 77 women with cervical lesions and 95 matched controls. Arginase activity was detected by colorimetric assay. Arginase mRNA expression and HPV viral load were evaluated by quantitative real time PCR and anti-HPV16 antibodies were assessed by ELISA.<br />Results: Compared to controls, the arginase activity was higher among women with cervicitis / low grade squamous intraepithelial lesions (LSIL) (OR: 1.872, 95% CI: 0.833-4.210), and also among women with high-grade squamous intraepithelial lesions (HSIL) / squamous cell carcinoma (SCC) (OR: 3.358, 95% CI: 1.670-8.910). Compared to controls, mRNA expression was significantly upregulated in women with cervical cervicitis and SIL for ARG1, and in women with cancer lesions for ARG2. Arginase activity was positively correlated to ARG2 mRNA expression but not to ARG1. High arginase activity was associated with HPV16, high levels of HPV viral load, and low levels of anti-HPV16 antibodies.<br />Conclusions: Our findings demonstrated that arginase activity and isoforms expression were enhanced in women with HPV-related precancerous lesions and cervical cancer. Further studies are needed to identify how arginase enzyme induces disease progression and severity.<br /> (Copyright © 2022. Published by Elsevier GmbH.)

Details

Language :
English
ISSN :
1878-3279
Volume :
227
Issue :
2
Database :
MEDLINE
Journal :
Immunobiology
Publication Type :
Academic Journal
Accession number :
35220072
Full Text :
https://doi.org/10.1016/j.imbio.2022.152189