Association between mRNA expression of chemotherapy-related genes and clinicopathological features in colorectal cancer: A large-scale population analysis

To establish the individualized treatment of patients with colorectal cancer, factors associated with chemotherapeutic effects should be identified. However, to the best of our knowledge, few studies are available on this topic, although it is known that the prognosis of patients and sensitivity to...

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Veröffentlicht in:International journal of molecular medicine 2016-02, Vol.37 (2), p.319-328
Hauptverfasser: SHIMAMOTO, YUJI, NUKATSUKA, MAMORU, TAKECHI, TEIJI, FUKUSHIMA, MASAKAZU
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container_title International journal of molecular medicine
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creator SHIMAMOTO, YUJI
NUKATSUKA, MAMORU
TAKECHI, TEIJI
FUKUSHIMA, MASAKAZU
description To establish the individualized treatment of patients with colorectal cancer, factors associated with chemotherapeutic effects should be identified. However, to the best of our knowledge, few studies are available on this topic, although it is known that the prognosis of patients and sensitivity to chemotherapy depend on the location of the tumor and that the tumor location is important for individualized treatment. In this study, primary tumors obtained from 1,129 patients with colorectal cancer were used to measure the mRNA expression levels of the following genes associated with the effects of standard chemotherapy for colorectal cancer: 5-fluorouracil (5-FU)-related thymidylate synthase (TYMS), dihydropyrimidine dehydrogenase (DPYD) and thymidine phosphorylase (TYMP); folate-related dihydrofolate reductase (DHFR), folylpolyglutamate synthase (FPGS) and gamma-glutamyl hydrolase (GGH); irinotecan-related topoisomerase I (TOP1); oxaliplatin-related excision repair cross-complementing 1 (ERCC1); biologic agent-related vascular endothelial growth factor (VEGF) and epidermal growth factor receptor (EGFR). Large-scale population analysis was performed to determine the association of gene expression with the clinicopathological features, in particular, the location of the colorectal cancer. From the results of our analysis of the mRNA expression of these 10 genes, we noted the strongest correlation between DPYD and TYMP, followed by TYMS and DHFR. The location of the colorectal cancer was classified into 4 regions (the right- and left-sided colon, rectosigmoid and rectum) and was compared with gene expression. A significant difference in all genes, apart from VEGF, was noted. Of the remaining 9 genes, the highest expression of TYMS and DPYD was observed in the right-sided colon; the highest expression of GGH and EGFR was noted in the left-sided colon; the highest expression of DHFR, FPGS, TOP1 and ERCC1 was noted in the rectosigmoid, whereas TYMP expression was approximately equivalent in the right-sided colon and rectum, and higher than that in other locations. The data generated from this study may prove to be useful for the development of individualized chemotherapeutic treatments for patients with colorectal cancer, and will mean that the tumor location is taken into account.
doi_str_mv 10.3892/ijmm.2015.2427
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However, to the best of our knowledge, few studies are available on this topic, although it is known that the prognosis of patients and sensitivity to chemotherapy depend on the location of the tumor and that the tumor location is important for individualized treatment. In this study, primary tumors obtained from 1,129 patients with colorectal cancer were used to measure the mRNA expression levels of the following genes associated with the effects of standard chemotherapy for colorectal cancer: 5-fluorouracil (5-FU)-related thymidylate synthase (TYMS), dihydropyrimidine dehydrogenase (DPYD) and thymidine phosphorylase (TYMP); folate-related dihydrofolate reductase (DHFR), folylpolyglutamate synthase (FPGS) and gamma-glutamyl hydrolase (GGH); irinotecan-related topoisomerase I (TOP1); oxaliplatin-related excision repair cross-complementing 1 (ERCC1); biologic agent-related vascular endothelial growth factor (VEGF) and epidermal growth factor receptor (EGFR). 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The data generated from this study may prove to be useful for the development of individualized chemotherapeutic treatments for patients with colorectal cancer, and will mean that the tumor location is taken into account.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>26676887</pmid><doi>10.3892/ijmm.2015.2427</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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source Spandidos Publications Journals; MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Adult
Aged
Aged, 80 and over
Analysis
Angiogenesis
Camptothecin - administration & dosage
Camptothecin - analogs & derivatives
Cancer
Cancer therapies
Care and treatment
Cell growth
Chemotherapy
chemotherapy-related genes
clinicopathological features
Colorectal cancer
Colorectal Neoplasms - drug therapy
Colorectal Neoplasms - genetics
Colorectal Neoplasms - pathology
Deoxyribonucleic acid
Dihydrofolate reductase
DNA
DNA Topoisomerases, Type I - biosynthesis
DNA Topoisomerases, Type I - genetics
DNA-Binding Proteins - biosynthesis
DNA-Binding Proteins - genetics
Endonucleases - biosynthesis
Endonucleases - genetics
Enzymes
Female
Fluorouracil - administration & dosage
gamma-Glutamyl Hydrolase - biosynthesis
gamma-Glutamyl Hydrolase - genetics
Gene Expression Regulation, Neoplastic - drug effects
Genetic aspects
Histology
Humans
Lymphatic system
Male
Medical prognosis
Messenger RNA
Metabolism
Metabolites
Metastasis
Middle Aged
mRNA expression
Organoplatinum Compounds - administration & dosage
Peptide Synthases - biosynthesis
Peptide Synthases - genetics
Physiological aspects
population analysis
Prognosis
Receptor, Epidermal Growth Factor - biosynthesis
Receptor, Epidermal Growth Factor - genetics
RNA, Messenger - biosynthesis
Tetrahydrofolate Dehydrogenase - biosynthesis
Tetrahydrofolate Dehydrogenase - genetics
Thymidine Phosphorylase - biosynthesis
Thymidine Phosphorylase - genetics
Tumors
Vascular endothelial growth factor
Vitamin B
title Association between mRNA expression of chemotherapy-related genes and clinicopathological features in colorectal cancer: A large-scale population analysis
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