Fas cell surface death receptor/Fas ligand genetic variants in gastric cancer patients: A case-control study

Background & objectives: Various studies have suggested a correlation between Fas cell surface death receptor/Fas ligand (FAS/FASL) variants and multiple types of cancers. The present study aimed to investigate the association between FAS-670A/G and FASL-844C/T and the synergistic effects of bot...

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Main Authors: Rezvan Asgari, Ali Bidmeshkipour, Kamran Mansouri, Mitra Bakhtiari, Hadi Mozafari, Amir Abdolmaleki
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2022-01-01
Series:Indian Journal of Medical Research
Subjects:
Online Access:http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2022;volume=156;issue=1;spage=77;epage=82;aulast=Asgari
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author Rezvan Asgari
Ali Bidmeshkipour
Kamran Mansouri
Mitra Bakhtiari
Hadi Mozafari
Amir Abdolmaleki
author_facet Rezvan Asgari
Ali Bidmeshkipour
Kamran Mansouri
Mitra Bakhtiari
Hadi Mozafari
Amir Abdolmaleki
author_sort Rezvan Asgari
collection DOAJ
description Background & objectives: Various studies have suggested a correlation between Fas cell surface death receptor/Fas ligand (FAS/FASL) variants and multiple types of cancers. The present study aimed to investigate the association between FAS-670A/G and FASL-844C/T and the synergistic effects of both variants on the risk of gastric cancer (GC) in the Kurdish population of west of Iran. Methods: This study was conducted by polymerase chain reaction-restriction fragment length polymorphism technique using MvaI and BsrDI restriction enzymes in 98 GC patients and 103 healthy control individuals. Results: According to the obtained results, a significant association (P=0.008) of FASL polymorphism among GC patients and the control group was detected. Furthermore, no significant differences were found in the FAS polymorphism frequencies between GC patients and the control group. Codominant and dominant models in FASL polymorphism showed significant protective effects against GC [odds ratio (OR)=0.307, 95% confidence interval (CI) (0.134-0.705), P=0.005; OR=0.205, 95% CI (0.058-0.718), P=0.013 and OR=0.295, 95% CI (0.129-0.673), P=0.004 for models of codominant CC vs. CT, codominant CC vs. TT and dominant, respectively]. Furthermore, the presence of both FAS-670G and FASL-844T alleles represented a significant protective effect against GC occurrence [OR=0.420, 95% CI (0.181-0.975), P=0.043]. Interpretation & conclusions: So far, we believe this is the first study, the results of which suggest that FASL gene variation and its synergistic effects with FAS gene could be associated with the risk of GC in the Kurdish population in the west of Iran.
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spelling doaj.art-89d6b2f3ba334e19bcf9347e159a10182023-01-12T11:56:38ZengWolters Kluwer Medknow PublicationsIndian Journal of Medical Research0971-59162022-01-011561778210.4103/ijmr.IJMR_2058_19Fas cell surface death receptor/Fas ligand genetic variants in gastric cancer patients: A case-control studyRezvan AsgariAli BidmeshkipourKamran MansouriMitra BakhtiariHadi MozafariAmir AbdolmalekiBackground & objectives: Various studies have suggested a correlation between Fas cell surface death receptor/Fas ligand (FAS/FASL) variants and multiple types of cancers. The present study aimed to investigate the association between FAS-670A/G and FASL-844C/T and the synergistic effects of both variants on the risk of gastric cancer (GC) in the Kurdish population of west of Iran. Methods: This study was conducted by polymerase chain reaction-restriction fragment length polymorphism technique using MvaI and BsrDI restriction enzymes in 98 GC patients and 103 healthy control individuals. Results: According to the obtained results, a significant association (P=0.008) of FASL polymorphism among GC patients and the control group was detected. Furthermore, no significant differences were found in the FAS polymorphism frequencies between GC patients and the control group. Codominant and dominant models in FASL polymorphism showed significant protective effects against GC [odds ratio (OR)=0.307, 95% confidence interval (CI) (0.134-0.705), P=0.005; OR=0.205, 95% CI (0.058-0.718), P=0.013 and OR=0.295, 95% CI (0.129-0.673), P=0.004 for models of codominant CC vs. CT, codominant CC vs. TT and dominant, respectively]. Furthermore, the presence of both FAS-670G and FASL-844T alleles represented a significant protective effect against GC occurrence [OR=0.420, 95% CI (0.181-0.975), P=0.043]. Interpretation & conclusions: So far, we believe this is the first study, the results of which suggest that FASL gene variation and its synergistic effects with FAS gene could be associated with the risk of GC in the Kurdish population in the west of Iran.http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2022;volume=156;issue=1;spage=77;epage=82;aulast=Asgarifas-670a/g - fasl-844c/t - gastric cancer - synergistic effect - variant
spellingShingle Rezvan Asgari
Ali Bidmeshkipour
Kamran Mansouri
Mitra Bakhtiari
Hadi Mozafari
Amir Abdolmaleki
Fas cell surface death receptor/Fas ligand genetic variants in gastric cancer patients: A case-control study
Indian Journal of Medical Research
fas-670a/g - fasl-844c/t - gastric cancer - synergistic effect - variant
title Fas cell surface death receptor/Fas ligand genetic variants in gastric cancer patients: A case-control study
title_full Fas cell surface death receptor/Fas ligand genetic variants in gastric cancer patients: A case-control study
title_fullStr Fas cell surface death receptor/Fas ligand genetic variants in gastric cancer patients: A case-control study
title_full_unstemmed Fas cell surface death receptor/Fas ligand genetic variants in gastric cancer patients: A case-control study
title_short Fas cell surface death receptor/Fas ligand genetic variants in gastric cancer patients: A case-control study
title_sort fas cell surface death receptor fas ligand genetic variants in gastric cancer patients a case control study
topic fas-670a/g - fasl-844c/t - gastric cancer - synergistic effect - variant
url http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2022;volume=156;issue=1;spage=77;epage=82;aulast=Asgari
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AT kamranmansouri fascellsurfacedeathreceptorfasligandgeneticvariantsingastriccancerpatientsacasecontrolstudy
AT mitrabakhtiari fascellsurfacedeathreceptorfasligandgeneticvariantsingastriccancerpatientsacasecontrolstudy
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