A DNA adductome analysis revealed a reduction in the global level of C5-hydroxymethyl-2′-deoxycytidine in the non-tumoral upper urinary tract mucosa of urothelial carcinoma patients

Abstract Background DNA adducts, covalent modifications to DNA due to exposure to specific carcinogens, cause the mispairing of DNA bases, which ultimately results in DNA mutations. DNA methylation in the promoter region, another type of DNA base modification, alters the DNA transcription process, a...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Yuto Matsushita, Yuji Iwashita, Shunsuke Ohtsuka, Ippei Ohnishi, Takashi Yamashita, Hideaki Miyake, Haruhiko Sugimura
Formato: article
Lenguaje:EN
Publicado: BMC 2021
Materias:
Acceso en línea:https://doaj.org/article/fb0898992ccc409bba965536dc3ca1d4
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:fb0898992ccc409bba965536dc3ca1d4
record_format dspace
spelling oai:doaj.org-article:fb0898992ccc409bba965536dc3ca1d42021-12-05T12:10:41ZA DNA adductome analysis revealed a reduction in the global level of C5-hydroxymethyl-2′-deoxycytidine in the non-tumoral upper urinary tract mucosa of urothelial carcinoma patients10.1186/s41021-021-00228-91880-7062https://doaj.org/article/fb0898992ccc409bba965536dc3ca1d42021-12-01T00:00:00Zhttps://doi.org/10.1186/s41021-021-00228-9https://doaj.org/toc/1880-7062Abstract Background DNA adducts, covalent modifications to DNA due to exposure to specific carcinogens, cause the mispairing of DNA bases, which ultimately results in DNA mutations. DNA methylation in the promoter region, another type of DNA base modification, alters the DNA transcription process, and has been implicated in carcinogenesis in humans due to the down-regulation of tumor suppressor genes. Difficulties are associated with demonstrating the existence of DNA adducts or chemically modified bases in the human urological system. Apart from aristolochic acid-DNA adducts, which cause urothelial carcinoma and endemic nephropathy in a particular geographical area (Balkan), limited information is currently available on DNA adduct profiles in renal cell carcinoma and upper urinary tract urothelial carcinoma, including renal pelvic cancer and ureteral cancer. Method To elucidate the significance of DNA adducts in carcinogenesis in the urothelial system, we investigated 53 DNA adducts in the non-tumoral renal parenchyma and non-tumoral renal pelvis of patients with renal cell carcinoma, upper urinary tract urothelial carcinoma, and other diseases using liquid chromatography coupled with tandem mass spectrometry. A comparative analysis of tissue types, the status of malignancy, and clinical characteristics, including lifestyle factors, was performed. Results C5-Methyl-2′-deoxycytidine, C5-hydroxymethyl-2′-deoxycytidine (5hmdC), C5-formyl-2′-deoxycytidine, 2′-deoxyinosine, C8-oxo-2′-deoxyadenosine, and C8-oxo-2′-deoxyguanosine (8-OHdG) were detected in the renal parenchyma and renal pelvis. 8-OHdG was more frequently detected in the renal pelvis than in the renal cortex and medulla (p = 0.048 and p = 0.038, respectively). 5hmdC levels were significantly lower in the renal pelvis of urothelial carcinoma patients (n = 10) than in the urothelium of patients without urothelial carcinoma (n = 15) (p = 0.010). Regarding 5hmdC levels in the renal cortex and medulla, Spearman’s rank correlation test revealed a negative correlation between age and 5hmdC levels (r = − 0.46, p = 0.018 and r = − 0.45, p = 0.042, respectively). Conclusions The present results revealed a reduction of 5hmdC levels in the non-tumoral urinary tract mucosa of patients with upper urinary tract urothelial carcinoma. Therefore, the urothelial cell epithelia of patients with upper urinary tract cancer, even in non-cancerous areas, may be predisposed to urothelial cancer.Yuto MatsushitaYuji IwashitaShunsuke OhtsukaIppei OhnishiTakashi YamashitaHideaki MiyakeHaruhiko SugimuraBMCarticleDNA adductDNA adductomeDNA adductomicsC5-hydroxymethyl-2′-deoxycytidineRenal cell carcinomaUpper urinary tract urothelial carcinomaEcologyQH540-549.5GeneticsQH426-470ENGenes and Environment, Vol 43, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic DNA adduct
DNA adductome
DNA adductomics
C5-hydroxymethyl-2′-deoxycytidine
Renal cell carcinoma
Upper urinary tract urothelial carcinoma
Ecology
QH540-549.5
Genetics
QH426-470
spellingShingle DNA adduct
DNA adductome
DNA adductomics
C5-hydroxymethyl-2′-deoxycytidine
Renal cell carcinoma
Upper urinary tract urothelial carcinoma
Ecology
QH540-549.5
Genetics
QH426-470
Yuto Matsushita
Yuji Iwashita
Shunsuke Ohtsuka
Ippei Ohnishi
Takashi Yamashita
Hideaki Miyake
Haruhiko Sugimura
A DNA adductome analysis revealed a reduction in the global level of C5-hydroxymethyl-2′-deoxycytidine in the non-tumoral upper urinary tract mucosa of urothelial carcinoma patients
description Abstract Background DNA adducts, covalent modifications to DNA due to exposure to specific carcinogens, cause the mispairing of DNA bases, which ultimately results in DNA mutations. DNA methylation in the promoter region, another type of DNA base modification, alters the DNA transcription process, and has been implicated in carcinogenesis in humans due to the down-regulation of tumor suppressor genes. Difficulties are associated with demonstrating the existence of DNA adducts or chemically modified bases in the human urological system. Apart from aristolochic acid-DNA adducts, which cause urothelial carcinoma and endemic nephropathy in a particular geographical area (Balkan), limited information is currently available on DNA adduct profiles in renal cell carcinoma and upper urinary tract urothelial carcinoma, including renal pelvic cancer and ureteral cancer. Method To elucidate the significance of DNA adducts in carcinogenesis in the urothelial system, we investigated 53 DNA adducts in the non-tumoral renal parenchyma and non-tumoral renal pelvis of patients with renal cell carcinoma, upper urinary tract urothelial carcinoma, and other diseases using liquid chromatography coupled with tandem mass spectrometry. A comparative analysis of tissue types, the status of malignancy, and clinical characteristics, including lifestyle factors, was performed. Results C5-Methyl-2′-deoxycytidine, C5-hydroxymethyl-2′-deoxycytidine (5hmdC), C5-formyl-2′-deoxycytidine, 2′-deoxyinosine, C8-oxo-2′-deoxyadenosine, and C8-oxo-2′-deoxyguanosine (8-OHdG) were detected in the renal parenchyma and renal pelvis. 8-OHdG was more frequently detected in the renal pelvis than in the renal cortex and medulla (p = 0.048 and p = 0.038, respectively). 5hmdC levels were significantly lower in the renal pelvis of urothelial carcinoma patients (n = 10) than in the urothelium of patients without urothelial carcinoma (n = 15) (p = 0.010). Regarding 5hmdC levels in the renal cortex and medulla, Spearman’s rank correlation test revealed a negative correlation between age and 5hmdC levels (r = − 0.46, p = 0.018 and r = − 0.45, p = 0.042, respectively). Conclusions The present results revealed a reduction of 5hmdC levels in the non-tumoral urinary tract mucosa of patients with upper urinary tract urothelial carcinoma. Therefore, the urothelial cell epithelia of patients with upper urinary tract cancer, even in non-cancerous areas, may be predisposed to urothelial cancer.
format article
author Yuto Matsushita
Yuji Iwashita
Shunsuke Ohtsuka
Ippei Ohnishi
Takashi Yamashita
Hideaki Miyake
Haruhiko Sugimura
author_facet Yuto Matsushita
Yuji Iwashita
Shunsuke Ohtsuka
Ippei Ohnishi
Takashi Yamashita
Hideaki Miyake
Haruhiko Sugimura
author_sort Yuto Matsushita
title A DNA adductome analysis revealed a reduction in the global level of C5-hydroxymethyl-2′-deoxycytidine in the non-tumoral upper urinary tract mucosa of urothelial carcinoma patients
title_short A DNA adductome analysis revealed a reduction in the global level of C5-hydroxymethyl-2′-deoxycytidine in the non-tumoral upper urinary tract mucosa of urothelial carcinoma patients
title_full A DNA adductome analysis revealed a reduction in the global level of C5-hydroxymethyl-2′-deoxycytidine in the non-tumoral upper urinary tract mucosa of urothelial carcinoma patients
title_fullStr A DNA adductome analysis revealed a reduction in the global level of C5-hydroxymethyl-2′-deoxycytidine in the non-tumoral upper urinary tract mucosa of urothelial carcinoma patients
title_full_unstemmed A DNA adductome analysis revealed a reduction in the global level of C5-hydroxymethyl-2′-deoxycytidine in the non-tumoral upper urinary tract mucosa of urothelial carcinoma patients
title_sort dna adductome analysis revealed a reduction in the global level of c5-hydroxymethyl-2′-deoxycytidine in the non-tumoral upper urinary tract mucosa of urothelial carcinoma patients
publisher BMC
publishDate 2021
url https://doaj.org/article/fb0898992ccc409bba965536dc3ca1d4
work_keys_str_mv AT yutomatsushita adnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT yujiiwashita adnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT shunsukeohtsuka adnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT ippeiohnishi adnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT takashiyamashita adnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT hideakimiyake adnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT haruhikosugimura adnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT yutomatsushita dnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT yujiiwashita dnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT shunsukeohtsuka dnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT ippeiohnishi dnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT takashiyamashita dnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT hideakimiyake dnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
AT haruhikosugimura dnaadductomeanalysisrevealedareductioninthegloballevelofc5hydroxymethyl2deoxycytidineinthenontumoralupperurinarytractmucosaofurothelialcarcinomapatients
_version_ 1718372231108624384