Literature DB >> 29200707

WWOX rs11644322 Polymorphism, Gemcitabine, and Pancreatic Cancer.

Sora Yasri1, Viroj Wiwanitkit2, Beuy Joob3.   

Abstract

Entities:  

Year:  2017        PMID: 29200707      PMCID: PMC5687000          DOI: 10.4103/ijmpo.ijmpo_125_17

Source DB:  PubMed          Journal:  Indian J Med Paediatr Oncol        ISSN: 0971-5851


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Sir, The pancreatic cancer is a deadly gastrointestinal cancer. The treatment by chemotherapy is a present cancer therapy option. Gemcitabine is widely used for the management of pancreatic cancer.[1] The effect of genetic underlying factor in response to gemcitabine is interesting. Schirmer et al. reported that “WWOX rs11644322 represents a major predictive factor in gemcitabine-treated pancreatic cancer. Decreased WWOX expression may interfere with gemcitabine sensitivity.”[2] Schirmer et al. found that the survival period of the patients decreased in order if they present GG, GA, and AA genotypes, respectively.[2] Here, the authors would like to discuss on the finding based on the quantum medicine calculation as previously reported in referenced publications.[345] Theoretically, the three genotypes can be successfully expressed, but there will be the difference in degree of expression based on the starting molecular component. In translation, the final amount of product will vary on the variation on molecular weight of genetic component. From calculation, the molecular weight will be N + 302.26, N + 286.26, and N + 270.28, where N is the molecular weight of other nucleotides apart from the variant point, for GG, GA, and AA genotypes, respectively. It can be seen that the variation AA has the lowest amount of starting molecular component; hence, it might result in the lowest amount of final product which further implies the lowest amount of successful bringing of derived translated product and drug, gemcitabine.

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Conflicts of interest

There are no conflicts of interest.
  4 in total

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Authors:  Benjamin A Weinberg; Philip A Philip; Mohamed E Salem
Journal:  Clin Adv Hematol Oncol       Date:  2017-02

2.  Relevance of Sp Binding Site Polymorphism in WWOX for Treatment Outcome in Pancreatic Cancer.

Authors:  Markus A Schirmer; Claudia M Lüske; Sebastian Roppel; Alexander Schaudinn; Christian Zimmer; Ruben Pflüger; Martin Haubrock; Jacobe Rapp; Cenap Güngör; Maximilian Bockhorn; Thilo Hackert; Thomas Hank; Oliver Strobel; Jens Werner; Jakob R Izbicki; Steven A Johnsen; Jochen Gaedcke; Jürgen Brockmöller; B Michael Ghadimi
Journal:  J Natl Cancer Inst       Date:  2016-02-08       Impact factor: 13.506

3.  HSD11B1 rs846908 polymorphisms and tacrolimus concentrations: quantum chemical analysis and implication in patients with renal transplantation.

Authors:  Beuy Joob; Viroj Wiwanitkit
Journal:  J Nephropharmacol       Date:  2016-01-18

4.  ATP-binding cassette, sub-family B (MDR/TAP), member 1 (ABCB1) polymorphism and clopidogrel concentration in acute coronary syndrome: molecular change can explain the observed therapeutic concentration.

Authors:  Beuy Joob; Viroj Wiwanitkit
Journal:  Anatol J Cardiol       Date:  2016-04       Impact factor: 1.596

  4 in total

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