Improved detection and precise relative quantification of the urinary cancer metabolite biomarkers - Creatine riboside, creatinine riboside, creatine and creatinine by UPLC-ESI-MS/MS: Application to the NCI-Maryland cohort population controls and lung cancer cases.


Journal

Journal of pharmaceutical and biomedical analysis
ISSN: 1873-264X
Titre abrégé: J Pharm Biomed Anal
Pays: England
ID NLM: 8309336

Informations de publication

Date de publication:
30 Nov 2020
Historique:
received: 14 07 2020
revised: 11 08 2020
accepted: 12 08 2020
pubmed: 17 9 2020
medline: 22 6 2021
entrez: 16 9 2020
Statut: ppublish

Résumé

Creatine riboside (CR) is a novel metabolite of cancer metabolism. It is a urinary diagnostic biomarker of lung and liver cancer risk and prognosis. The level of CR is highly positive correlated in tumor and urine indicating that it is derived from human lung and liver cancers. A precise and sensitive ultra-pressure liquid chromatography-tandem mass spectrometry (UPLC-ESI-MS/MS) method was developed and validated for simultaneous quantification of the noninvasive biomarker CR, along with creatinine riboside (CNR), and their precursors creatine and creatinine, utilizing the labeled internal standard creatine riboside-

Identifiants

pubmed: 32937240
pii: S0731-7085(20)31482-5
doi: 10.1016/j.jpba.2020.113596
pmc: PMC7756200
mid: NIHMS1654398
pii:
doi:

Substances chimiques

2-(2-(3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl)-1-methylcarbamimidamido)acetic acid 0
Biomarkers, Tumor 0
Ribonucleosides 0
Creatinine AYI8EX34EU
Creatine MU72812GK0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113596

Subventions

Organisme : Intramural NIH HHS
ID : ZIA BC005708
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors disclose no potential conflict of interests.

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Auteurs

Daxesh P Patel (DP)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Gary T Pauly (GT)

Chemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, Fredrick, MD, USA.

Takeshi Tada (T)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Amelia L Parker (AL)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Leila Toulabi (L)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Yasuyuki Kanke (Y)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Takahiro Oike (T)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Kristopher W Krausz (KW)

Laboratory of Metabolism, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Frank J Gonzalez (FJ)

Laboratory of Metabolism, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Curtis C Harris (CC)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA. Electronic address: harrisc@mail.nih.gov.

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Classifications MeSH