Expression of tumor pyruvate kinase M2 isoform in plasma and stool of patients with colorectal cancer or adenomatous polyps.


Journal

BMC gastroenterology
ISSN: 1471-230X
Titre abrégé: BMC Gastroenterol
Pays: England
ID NLM: 100968547

Informations de publication

Date de publication:
29 Jul 2020
Historique:
received: 14 10 2019
accepted: 09 07 2020
entrez: 31 7 2020
pubmed: 31 7 2020
medline: 15 5 2021
Statut: epublish

Résumé

Tumor pyruvate kinase M2 isoform (tM2-PK), which is an isoform of PK-glycolytic enzyme and appears on the surface of cancerous proliferating cells, has been used as a diagnostic biomarker for colorectal cancer (CRC). The aim of this study was to evaluate the tM2-PK measurement test for the diagnosis of CRCs and adenomatous polyps in plasma and stool samples in an Iranian population. In this prospective study, a total of 226 stool and 178 plasma samples were received from patients referred to colonoscopy units. tM2-PK enzyme was measured using two separate ScheBo-Biotech-AG ELISA kits for stool and plasma samples. According to ROC curves, in the tumor group, at the cut-off value of 4 U/ml, the sensitivity of fecal tM2-PK test was 100% and the specificity was 68%, and in the polyp group, the sensitivity and specificity were 87 and 68%, respectively. For tumor detection in plasma specimens, a cut-off value > 25 U/ml has a sensitivity and specificity of 90.9 and 91.3%, respectively. Similarly, for polyp detection, a cut-off value > 19 U/ml has a sensitivity of 96.3% and the specificity of 85.5%. Based on our results, a cut-off range of 4.8-8 U/ml and >  8 U/ml could be used to detect polyp and tumor in stool samples, respectively. Similarly, a cut-off range of 19-25 U/ml and > 25 U/ml is recommended in plasma samples, suggesting tM2-PK test as a non-invasive assay to diagnose CRC and adenomatous polyps.

Sections du résumé

BACKGROUND BACKGROUND
Tumor pyruvate kinase M2 isoform (tM2-PK), which is an isoform of PK-glycolytic enzyme and appears on the surface of cancerous proliferating cells, has been used as a diagnostic biomarker for colorectal cancer (CRC). The aim of this study was to evaluate the tM2-PK measurement test for the diagnosis of CRCs and adenomatous polyps in plasma and stool samples in an Iranian population.
METHODS METHODS
In this prospective study, a total of 226 stool and 178 plasma samples were received from patients referred to colonoscopy units. tM2-PK enzyme was measured using two separate ScheBo-Biotech-AG ELISA kits for stool and plasma samples.
RESULTS RESULTS
According to ROC curves, in the tumor group, at the cut-off value of 4 U/ml, the sensitivity of fecal tM2-PK test was 100% and the specificity was 68%, and in the polyp group, the sensitivity and specificity were 87 and 68%, respectively. For tumor detection in plasma specimens, a cut-off value > 25 U/ml has a sensitivity and specificity of 90.9 and 91.3%, respectively. Similarly, for polyp detection, a cut-off value > 19 U/ml has a sensitivity of 96.3% and the specificity of 85.5%.
CONCLUSIONS CONCLUSIONS
Based on our results, a cut-off range of 4.8-8 U/ml and >  8 U/ml could be used to detect polyp and tumor in stool samples, respectively. Similarly, a cut-off range of 19-25 U/ml and > 25 U/ml is recommended in plasma samples, suggesting tM2-PK test as a non-invasive assay to diagnose CRC and adenomatous polyps.

Identifiants

pubmed: 32727566
doi: 10.1186/s12876-020-01377-x
pii: 10.1186/s12876-020-01377-x
pmc: PMC7388451
doi:

Substances chimiques

Biomarkers, Tumor 0
Isoenzymes 0
Pyruvate Kinase EC 2.7.1.40

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

241

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Auteurs

Farideh Rigi (F)

Razavi Cancer Research Center, Razavi Hospital, Imam Reza International University, Mashhad, Iran.
Department of Biotechnology, Faculty of Basic Science, Sabzevar Branch, Islamic Azad University, Sabzevar, Iran.

Aliakbar Jannatabad (A)

Department of Biotechnology, Faculty of Basic Science, Sabzevar Branch, Islamic Azad University, Sabzevar, Iran.

Azra Izanloo (A)

Razavi Cancer Research Center, Razavi Hospital, Imam Reza International University, Mashhad, Iran.

Reza Roshanravan (R)

Razavi Cancer Research Center, Razavi Hospital, Imam Reza International University, Mashhad, Iran.

Hamid Reza Hashemian (HR)

Razavi Cancer Research Center, Razavi Hospital, Imam Reza International University, Mashhad, Iran. hrhash1346@yahoo.com.

Mohammad Amin Kerachian (MA)

Medical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran. amin.kerachian@mail.mcgill.ca.
Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran. amin.kerachian@mail.mcgill.ca.
Cancer Genetics Research Unit, Reza Radiotherapy and Oncology Center, Mashhad, Iran. amin.kerachian@mail.mcgill.ca.

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Classifications MeSH