Faecal Diagnostic Biomarkers for Colorectal Cancer

Background: Colorectal cancer (CRC) is a major cause of cancer-related death worldwide. Cancer progression, including invasion and metastasis, is a major cause of death among CRC patients. Current methods for CRC screening commonly consist of a combination of faecal immunochemical test (FIT) for sto...

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Autores principales: Andrea Cruz, Carla M. Carvalho, Alexandra Cunha, Anais Crespo, Águeda Iglesias, Laura García-Nimo, Paulo P. Freitas, Joaquín Cubiella
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Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/f1a4b2170cee495791fe9393265f9ea5
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spelling oai:doaj.org-article:f1a4b2170cee495791fe9393265f9ea52021-11-11T15:35:27ZFaecal Diagnostic Biomarkers for Colorectal Cancer10.3390/cancers132155682072-6694https://doaj.org/article/f1a4b2170cee495791fe9393265f9ea52021-11-01T00:00:00Zhttps://www.mdpi.com/2072-6694/13/21/5568https://doaj.org/toc/2072-6694Background: Colorectal cancer (CRC) is a major cause of cancer-related death worldwide. Cancer progression, including invasion and metastasis, is a major cause of death among CRC patients. Current methods for CRC screening commonly consist of a combination of faecal immunochemical test (FIT) for stool occult blood detection and invasive procedures such as colonoscopy. Considering the slow progression of CRC, and that symptoms usually emerge at advanced stages, its early diagnostic can limit cancer’s spread and provide a successful treatment. Biomarkers have a high potential for the diagnosis of CRC in either blood or stool samples. Methods: In this study, we analysed the diagnostic value of six different biomarkers in stool samples of patients with CRC, advanced adenomas, other lesions and healthy individuals. We have also assessed the overall performance of the combination of these biomarkers for CRC detection. Results: The results indicate that haemoglobin (Hb) and M2-pyruvate kinase (M2-PK) levels were increased in CRC patients in comparison to the controls. Conversely, the concentrations of matrix metalloproteinase (MMP)-2, MMP-9, and tumour necrosis factor-alpha (TNF-α) were not significantly different between the tested groups. Conclusion: The combination of FIT-Hb with the M2-PK levels increased the specificity or sensitivity for CRC detection and thus present potential as faecal diagnostic biomarkers for CRC.Andrea CruzCarla M. CarvalhoAlexandra CunhaAnais CrespoÁgueda IglesiasLaura García-NimoPaulo P. FreitasJoaquín CubiellaMDPI AGarticlecolorectal canceradvanced adenomadiagnosisbiomarkersfaecal haemoglobinM2-PKNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENCancers, Vol 13, Iss 5568, p 5568 (2021)
institution DOAJ
collection DOAJ
language EN
topic colorectal cancer
advanced adenoma
diagnosis
biomarkers
faecal haemoglobin
M2-PK
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle colorectal cancer
advanced adenoma
diagnosis
biomarkers
faecal haemoglobin
M2-PK
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Andrea Cruz
Carla M. Carvalho
Alexandra Cunha
Anais Crespo
Águeda Iglesias
Laura García-Nimo
Paulo P. Freitas
Joaquín Cubiella
Faecal Diagnostic Biomarkers for Colorectal Cancer
description Background: Colorectal cancer (CRC) is a major cause of cancer-related death worldwide. Cancer progression, including invasion and metastasis, is a major cause of death among CRC patients. Current methods for CRC screening commonly consist of a combination of faecal immunochemical test (FIT) for stool occult blood detection and invasive procedures such as colonoscopy. Considering the slow progression of CRC, and that symptoms usually emerge at advanced stages, its early diagnostic can limit cancer’s spread and provide a successful treatment. Biomarkers have a high potential for the diagnosis of CRC in either blood or stool samples. Methods: In this study, we analysed the diagnostic value of six different biomarkers in stool samples of patients with CRC, advanced adenomas, other lesions and healthy individuals. We have also assessed the overall performance of the combination of these biomarkers for CRC detection. Results: The results indicate that haemoglobin (Hb) and M2-pyruvate kinase (M2-PK) levels were increased in CRC patients in comparison to the controls. Conversely, the concentrations of matrix metalloproteinase (MMP)-2, MMP-9, and tumour necrosis factor-alpha (TNF-α) were not significantly different between the tested groups. Conclusion: The combination of FIT-Hb with the M2-PK levels increased the specificity or sensitivity for CRC detection and thus present potential as faecal diagnostic biomarkers for CRC.
format article
author Andrea Cruz
Carla M. Carvalho
Alexandra Cunha
Anais Crespo
Águeda Iglesias
Laura García-Nimo
Paulo P. Freitas
Joaquín Cubiella
author_facet Andrea Cruz
Carla M. Carvalho
Alexandra Cunha
Anais Crespo
Águeda Iglesias
Laura García-Nimo
Paulo P. Freitas
Joaquín Cubiella
author_sort Andrea Cruz
title Faecal Diagnostic Biomarkers for Colorectal Cancer
title_short Faecal Diagnostic Biomarkers for Colorectal Cancer
title_full Faecal Diagnostic Biomarkers for Colorectal Cancer
title_fullStr Faecal Diagnostic Biomarkers for Colorectal Cancer
title_full_unstemmed Faecal Diagnostic Biomarkers for Colorectal Cancer
title_sort faecal diagnostic biomarkers for colorectal cancer
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/f1a4b2170cee495791fe9393265f9ea5
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