Literature DB >> 22346003

NQO1 C 609 T polymorphisms analyzed in a population from Kolkata, West Bengal.

Sanjit Mukherjee1, Keya Chaudhuri.   

Abstract

Entities:  

Year:  2011        PMID: 22346003      PMCID: PMC3277000          DOI: 10.4103/0971-6866.92083

Source DB:  PubMed          Journal:  Indian J Hum Genet        ISSN: 1998-362X


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Sir, The recent paper of Parihar and Chauhan[1] in your journal showed that the frequencies of different polymorphs of NQO1 genes were statistically distinct in the population residing in Vindhyan range, Madhya Pradesh, India, compared with the Caucasian and other Asian and European populations. NADP (H) Quinone Oxidoreductase 1 participates in detoxification of numerous compounds mainly by catalyzing the 2 electron reduction of the quinones to hydroquinones. Its polymorphic variant, C 609 T, is gaining much importance as it has a direct effect on the catalytic potential of the enzyme. The NQO1 variant form C 609 T, which leads to an amino acid change from Proline to Serine at codon position 187, exposes the enzyme to proteosomal degradation so that the available protein is less, and this leads to accumulation of Reactive Oxygen Species (ROS). The heterozygous carrier of this variant form has a 60% less catalytic efficiency, whereas a negligible amount of enzyme is found in homozygous mutant variant individuals, making the individuals more susceptible to carcinogenesis. This variant form of NQO1 is shown to be associated with an increased risk of acute myeloblastic leukemia[2] and many tobacco-associated cancers, namely lung cancer, colorectal cancer,[3] esophageal cancer[4] and, mostly, head and squamous cell carcinomas,[5] in many parts of the world. The use of tobacco and its associated products, either smoking or smokeless forms, or chewing arecanut as “pan masala” or “gutkha” is highly prevalent in south-east Asia, especially in the Indian subcontinent. Therefore, it is important to study the genetic predisposition of NQO1 polymorphism across various regions of the Indian subcontinent. Again, ethnicity is one of the main factors to be considered in genetic predisposition. However, very few studies exist depicting the prevalence of this NQO1 C 609 T genotype in the Indian subcontinent.[16] In this context, our pilot study examined the prevalence of NQO1 C 609 T polymorphism among 152 individuals from Kolkata, West Bengal [Table 1] in a different region of India compared with earlier studies. In our study, 78 (51.0%) individuals were found to carry minor T as heterozygous state whereas 13 (8.5%) individuals were homozygous mutants for this polymorphism. When stratified according to sex, both heterozygous and homozygous was found to be equally distributed [Table 1].
Table 1

Distribution of NQO1 genotypes among the study groups of Kolkata, West Bengal population

Distribution of NQO1 genotypes among the study groups of Kolkata, West Bengal population Interestingly, comparison of our results with the genotype frequencies observed in Caucasian, Chinese, Korean, Swedish, Iranian and Indian populations revealed that the population of this region of eastern India is distinct with respect to all other population except the Chinese, to which it bears close resemblance [Table 2].
Table 2

Distribution of NQO1 genotypes among the study groups of different Asian and European populations

Distribution of NQO1 genotypes among the study groups of different Asian and European populations Moreover, the frequencies of TT and CT genotypes are higher in this population compared with those from other parts of India. Further studies need to be focused on the correlation of NQO1 genotypes with smoking/chewing habits, and the association with oral cancer and precancer would predict the risk of carcinogenesis in this population.[8]
  7 in total

1.  NQO1 C609T polymorphism associated with esophageal cancer and gastric cardiac carcinoma in North China.

Authors:  Jian-Hui Zhang; Yan Li; Rui Wang; Helen Geddert; Wei Guo; Deng-Gui Wen; Zhi-Feng Chen; Li-Zhen Wei; Gang Kuang; Ming He; Li-Wei Zhang; Ming-Li Wu; Shi-Jie Wang
Journal:  World J Gastroenterol       Date:  2003-07       Impact factor: 5.742

2.  Influence of CYP1A1, GSTM1, GSTT1, and NQO1 genotypes and cumulative smoking dose on lung cancer risk in a Swedish population.

Authors:  Anna-Karin Alexandrie; Fredrik Nyberg; Margareta Warholm; Agneta Rannug
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2004-06       Impact factor: 4.254

3.  NAD(P)H:quinone oxidoreductase 1 (NQO1) Pro187Ser polymorphism and colorectal cancer predisposition in the ethnic Kashmiri population.

Authors:  A Syed Sameer; Zaffar A Shah; Nidda Syeed; Roohi Rasool; Dil Afroze; Mushtaq A Siddiqi
Journal:  Asian Pac J Cancer Prev       Date:  2010

4.  NAD(P)H:quinone oxidoreductase 1 (NQO1) Pro187Ser polymorphism and the risk of lung, bladder, and colorectal cancers: a meta-analysis.

Authors:  Chun Chao; Zuo-Feng Zhang; Julien Berthiller; Paolo Boffetta; Mia Hashibe
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2006-05       Impact factor: 4.254

Review 5.  NQO1 polymorphisms and de novo childhood leukemia: a HuGE review and meta-analysis.

Authors:  Neela Guha; Jeffrey S Chang; Anand P Chokkalingam; Joseph L Wiemels; Martyn T Smith; Patricia A Buffler
Journal:  Am J Epidemiol       Date:  2008-10-22       Impact factor: 4.897

6.  The NQO1 allelic frequency in hindu population of central India varies from that of other Asian populations.

Authors:  Sher S Parihar; U K Chauhan
Journal:  Indian J Hum Genet       Date:  2010-09

7.  Association of the GSTP1 and NQO1 polymorphisms and head and neck squamous cell carcinoma risk.

Authors:  Chang Gun Cho; Seok Ki Lee; Soon-Yhul Nam; Moo-Song Lee; Sang-Wook Lee; Eun Kyung Choi; Heon Joo Park; Sang Yoon Kim
Journal:  J Korean Med Sci       Date:  2006-12       Impact factor: 2.153

  7 in total

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