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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MDPI AG
2021
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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) |
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colorectal cancer advanced adenoma diagnosis biomarkers faecal haemoglobin M2-PK Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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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 |
work_keys_str_mv |
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