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Association of a common genetic variant (insertion/deletion) in ACE gene with prostate cancer susceptibility in a Tunisian population

BACKGROUND: Angiotensin‐converting enzyme (ACE) plays a pivotal role in several pathologies including cancers. The association of insertion/deletion (I/D) polymorphism of the ACE gene with prostate cancer (PC) risk remains controversial. We aimed to investigate for the first time, to our Knowledge,...

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Autores principales: Said, Rahma, Jenni, Rim, Boussetta, Sami, Ammous, Feryel, Zouari, Skander, Zaghbib, Selim, Chakroun, Marouene, Derouiche, Amine, Chebil, Mohamed, Ouerhani, Slah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8761439/
https://www.ncbi.nlm.nih.gov/pubmed/34799866
http://dx.doi.org/10.1002/jcla.24129
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author Said, Rahma
Jenni, Rim
Boussetta, Sami
Ammous, Feryel
Zouari, Skander
Zaghbib, Selim
Chakroun, Marouene
Derouiche, Amine
Chebil, Mohamed
Ouerhani, Slah
author_facet Said, Rahma
Jenni, Rim
Boussetta, Sami
Ammous, Feryel
Zouari, Skander
Zaghbib, Selim
Chakroun, Marouene
Derouiche, Amine
Chebil, Mohamed
Ouerhani, Slah
author_sort Said, Rahma
collection PubMed
description BACKGROUND: Angiotensin‐converting enzyme (ACE) plays a pivotal role in several pathologies including cancers. The association of insertion/deletion (I/D) polymorphism of the ACE gene with prostate cancer (PC) risk remains controversial. We aimed to investigate for the first time, to our Knowledge, in North Africa the potential relationship between ACE I/D polymorphism with PC susceptibility and clinical outcomes of PC patients. METHODS: This case‐control study included 143 healthy individuals and 124 patients diagnosed with PC. Using genomic DNA, the samples were genotyped for ACE I/D polymorphism by polymerase chain reaction (PCR). RESULTS: We found that The D allele is significantly associated with an increased risk of PC and D/D + D/I genotypes were at 3 times increased risk of PC ([p = 0.005], OR = 2.95, IC 95% = 1.26–7.09) compared with I/I genotype (p = 0.003, OR = 0.3, IC 95% = 0.12–0.74). We observed an association between D/D and D/I genotypes with advanced age (≥70 years) (p = 0.014; r (2) = 0.22). Furthermore, there is a significant prediction of advanced Gleason score ≥8 based on epidemiological parameters and ACE genotype (p = 0.000; R(2) = 0.349), although no significant association was observed with stage and metastasis. CONCLUSION: The ACE I/D polymorphism is likely to predispose to PC and could play a role in PC progression and aggressiveness.
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spelling pubmed-87614392022-01-20 Association of a common genetic variant (insertion/deletion) in ACE gene with prostate cancer susceptibility in a Tunisian population Said, Rahma Jenni, Rim Boussetta, Sami Ammous, Feryel Zouari, Skander Zaghbib, Selim Chakroun, Marouene Derouiche, Amine Chebil, Mohamed Ouerhani, Slah J Clin Lab Anal Research Articles BACKGROUND: Angiotensin‐converting enzyme (ACE) plays a pivotal role in several pathologies including cancers. The association of insertion/deletion (I/D) polymorphism of the ACE gene with prostate cancer (PC) risk remains controversial. We aimed to investigate for the first time, to our Knowledge, in North Africa the potential relationship between ACE I/D polymorphism with PC susceptibility and clinical outcomes of PC patients. METHODS: This case‐control study included 143 healthy individuals and 124 patients diagnosed with PC. Using genomic DNA, the samples were genotyped for ACE I/D polymorphism by polymerase chain reaction (PCR). RESULTS: We found that The D allele is significantly associated with an increased risk of PC and D/D + D/I genotypes were at 3 times increased risk of PC ([p = 0.005], OR = 2.95, IC 95% = 1.26–7.09) compared with I/I genotype (p = 0.003, OR = 0.3, IC 95% = 0.12–0.74). We observed an association between D/D and D/I genotypes with advanced age (≥70 years) (p = 0.014; r (2) = 0.22). Furthermore, there is a significant prediction of advanced Gleason score ≥8 based on epidemiological parameters and ACE genotype (p = 0.000; R(2) = 0.349), although no significant association was observed with stage and metastasis. CONCLUSION: The ACE I/D polymorphism is likely to predispose to PC and could play a role in PC progression and aggressiveness. John Wiley and Sons Inc. 2021-11-19 /pmc/articles/PMC8761439/ /pubmed/34799866 http://dx.doi.org/10.1002/jcla.24129 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Said, Rahma
Jenni, Rim
Boussetta, Sami
Ammous, Feryel
Zouari, Skander
Zaghbib, Selim
Chakroun, Marouene
Derouiche, Amine
Chebil, Mohamed
Ouerhani, Slah
Association of a common genetic variant (insertion/deletion) in ACE gene with prostate cancer susceptibility in a Tunisian population
title Association of a common genetic variant (insertion/deletion) in ACE gene with prostate cancer susceptibility in a Tunisian population
title_full Association of a common genetic variant (insertion/deletion) in ACE gene with prostate cancer susceptibility in a Tunisian population
title_fullStr Association of a common genetic variant (insertion/deletion) in ACE gene with prostate cancer susceptibility in a Tunisian population
title_full_unstemmed Association of a common genetic variant (insertion/deletion) in ACE gene with prostate cancer susceptibility in a Tunisian population
title_short Association of a common genetic variant (insertion/deletion) in ACE gene with prostate cancer susceptibility in a Tunisian population
title_sort association of a common genetic variant (insertion/deletion) in ace gene with prostate cancer susceptibility in a tunisian population
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8761439/
https://www.ncbi.nlm.nih.gov/pubmed/34799866
http://dx.doi.org/10.1002/jcla.24129
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