Association of genetic polymorphism of glutathione S-transferases with colorectal cancer susceptibility in snuff (Naswar) addicts.


Journal

Brazilian journal of biology = Revista brasleira de biologia
ISSN: 1678-4375
Titre abrégé: Braz J Biol
Pays: Brazil
ID NLM: 101129542

Informations de publication

Date de publication:
2022
Historique:
received: 26 02 2022
accepted: 17 05 2022
entrez: 8 6 2022
pubmed: 9 6 2022
medline: 11 6 2022
Statut: epublish

Résumé

The current study aimed to investigate the relationship between polymorphisms in detoxifying (GSTM1, GSTT1, and GSTP1) genes and their association with colorectal cancer (CRC) in tobacco addicts of Pashtun ethnicity. Polymorphisms in the selected genes were genotyped in a case-control study consisting of 100 histologically confirmed male CRC patients and 100 birth-year and gender-matched healthy controls using the PCR-RFLP method. The GSTM1 null, and GSTT1 null genotypes were significantly contributed to the risk of CRC in the cases (OR= 3.131, 95% CI: 1.451-6.758, P = 0.004, and OR= 3.541, 95% CI: 1.716-7.306, P = 0.001, respectively), whereas the association observed for GSTP1 Val/Val (1.139, 95% CI: 0.356-3.644, P = 0.826) did not show statistical significance. The combined GSTM1 null and GSTT1 null showed a 41-fold increased risk (95% CI: 4.945-351.950, P = 0.001), while, the combined GSTM1 null and GSTP1 Ile/Val or Val/Val variant genotypes exhibited about 3-fold (95% CI: 1.196-7.414, P = 0.019) increased risk to CRC. Similarly, the combined GSTT1 null and GSTP1 Ile/Val or Val/Val variant genotypes showed about a 3-fold (95% CI: 1.285-8.101, P = 0.013) increased risk of CRC. In the combination of three GST genotypes, the GSTM1 null, GSTT1 null, and GSTP1 Ile/Val or Val/Val variant genotypes demonstrated a more than a 22-fold (95% CI: 2.441-212.106, P = 0.006) increased risk of CRC. Our findings suggest that GSTM1 and GSTT1 polymorphism and its combination with GSTP1 may be associated with CRC susceptibility in the Naswar addicted Pashtun population of Khyber Pakhtunkhwa, Pakistan.

Identifiants

pubmed: 35674599
pii: S1519-69842024000100324
doi: 10.1590/1519-6984.261509
pii:
doi:

Substances chimiques

glutathione S-transferase T1 EC 2.5.1.-
GSTP1 protein, human EC 2.5.1.18
Glutathione S-Transferase pi EC 2.5.1.18
Glutathione Transferase EC 2.5.1.18
glutathione S-transferase M1 EC 2.5.1.18

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e261509

Auteurs

A Khan (A)

University of Peshawar, Department of Zoology, Peshawar, Khyber Pakhtunkhwa, Pakistan.

F Jahan (F)

Shaheed Benazir Bhutto Women University Peshawar, Department of Zoology, Peshawar, Khyber Pakhtunkhwa, Pakistan.

M Zahoor (M)

University of Malakand, Department of Biochemistry, Chakdara, Lower Dir, Pakistan.

R Ullah (R)

King Saud University, College of Pharmacy, Department of Pharmacognosy, Riyadh, Saudi Arabia.

G M Albadrani (GM)

Princess Nourah bint Abdulrahman University, College of Science, Department of Biology, Riyadh, Saudi Arabia.

H R H Mohamed (HRH)

Cairo University, Faculty of Science, Department of Zoology, Giza, Egypt.

M Khisroon (M)

University of Peshawar, Department of Zoology, Peshawar, Khyber Pakhtunkhwa, Pakistan.

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Classifications MeSH