Pharmacogenetics research on chemotherapy resistance in colorectal cancer over the last 20 years

During the past two decades the first sequencing of the human genome was performed showing its high degree of inter-individual differentiation,as a result of large international research projects(Human Genome Project,the 1000 Genomes Project International HapMap Project,and Programs for Genomic Appl...

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Published inWorld journal of gastroenterology : WJG Vol. 20; no. 29; pp. 9775 - 9827
Main Author Panczyk, Mariusz
Format Journal Article
LanguageEnglish
Published United States Baishideng Publishing Group Inc 07.08.2014
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Summary:During the past two decades the first sequencing of the human genome was performed showing its high degree of inter-individual differentiation,as a result of large international research projects(Human Genome Project,the 1000 Genomes Project International HapMap Project,and Programs for Genomic Applications NHLBI-PGA).This period was also a time of intensive development of molecular biology techniques and enormous knowledge growth in the biology of cancer.For clinical use in the treatment of patients with colorectal cancer(CRC),in addition to fluoropyrimidines,another two new cytostatic drugs were allowed:irinotecan and oxaliplatin.Intensive research into new treatment regimens and a new generation of drugs used in targeted therapy has also been conducted.The last 20years was a time of numerous in vitro and in vivo studies on the molecular basis of drug resistance.One of the most important factors limiting the effectiveness of chemotherapy is the primary and secondary resistance of cancer cells.Understanding the genetic factors and mechanisms that contribute to the lack of or low sensitivity of tumour tissue to cytostatics is a key element in the currently developing trend of personalized medicine.Scientists hope to increase the percentage of positive treatment response in CRC patients due to practical applications of pharmacogenetics/pharmacogenomics.Over the past 20 years the clinical usability of different predictive markers has been tested among which only a few have been confirmed to have high application potential.This review is a synthetic presentation of drug resistance in the context of CRC patient chemotherapy.The multifactorial nature and volume of the issues involved do not allow the author to present a comprehensive study on this subject in one review.
Bibliography:Mariusz Panczyk;Laboratory of Molecular Diagnostics and Pharmacogenomics,Department of Pharmaceutical Biochemistry,Medical University of Lodz;Division of Teaching and Outcomes of Education,Faculty of Health Science,Medical University of Warsaw
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Telephone: +48-225-720490 Fax: +48-225-720491
Author contributions: Panczyk M designed and wrote the manuscript.
Correspondence to: Mariusz Panczyk, PharmD, PhD, Division of Teaching and Outcomes of Education, Faculty of Health Science, Medical University of Warsaw, Zwirki i Wigury 61, 02-091 Warsaw, Poland. mariusz.panczyk@wum.edu.pl
ISSN:1007-9327
2219-2840
2219-2840
DOI:10.3748/wjg.v20.i29.9775