Glutathione S-Transferase, PI

Alternative Names

  • GSTP1
  • Glutathione S-Transferase 3
  • GST3
  • GST, Class PI
  • Fatty Acid Ethyl Ester Synthase III, Myocardial
  • FAEES3
  • Glutathione S-Transferase Pi Pseudogene
  • GSTPP
Back to search Result
OMIM Number

134660

NCBI Gene ID

2950

Uniprot ID

P09211

Length

2,842 bases

No. of Exons

7

No. of isoforms

1

Protein Name

Glutathione S-transferase P

Molecular Mass

23356 Da

Amino Acid Count

210

Genomic Location

chr11:67,583,812-67,586,653

Gene Map Locus
11q13.2

Description

The glutathione S transferase (GST) family is a major part of cellular defense mechanisms against endogenous and exogenous substances, many of which have carcinogenic potential. Alteration in the expression level or structure of the glutathione-S-transferase (GST) enzymes may lead to inadequate detoxification of potential carcinogens and consequently contribute to cancer development. The GSTP1 gene is a member of the glutathione S-transferases (GSTs) family of proteins; it encodes a phase II metabolic enzyme that detoxifies reactive electrophilic intermediates.  GSTP1 is expressed in normal tissues at variable levels in different cell types.  It is frequently over-expressed in many human cancers and the expression increases with tumor progression and is associated with a more aggressive biology, poor patient survival, and resistance to therapy.

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_000852.4:c.313A>GLebanon; United Arab E...NC_000011.10:g.67585218A>GBenignDrug Response, Uncertain SignificanceBreast CancerNG_012075.1:g.6624A>G; NM_000852.4:c.313A>G; NP_000843.1:p.Ile105Val169537340

Other Reports

Jordan

Khabaz (2012) investigated the possible impact of Ile105Val GSTP1 polymorphism on susceptibility to colorectal cancer in Jordan.  Ninety tissue samples previously diagnosed with colorectal carcinoma, and 56 non-cancerous colon tissues were analyzed.  No statistically significant differences were found between colorectal cancer cases and controls for the GSTP1 Ile/Ile, Ile/Val and Val/Val genotypes.  Khabaz (2012) concluded that the GSTP1 Ile105Val polymorphism was not associated with risk in colorectal cancer cases in Jordan stratified by age, sex, site, grade or tumor stage.  In a subsequent study, Khabaz et al. (2014) investigated the GSTP1 polymorphism in 100-tissue samples previously diagnosed as breast carcinoma, and in 48 non-cancer age-matched breast tissues.  Among breast cancer cases, 58%, 40%, and 2% were homozygous (Ile/Ile), heterozygous (Ile/Val), and homozygous (Val/Val), respectively.  In the control group, 58%, 38%, and 4% were homozygous (Ile/Ile), heterozygous (Ile/Val), and homozygous (Val/Val), respectively. Khabaz et al. (2014) excluded a possible involvement of the GSTP1 gene polymorphism in susceptibility to breast carcinoma in the North Jordanian female population.

© CAGS 2024. All rights reserved.