Screening for colorectal cancer leading into a new decade: the “Roaring ‘20s” for epigenetic biomarkers?

Detalhes bibliográficos
Autor(a) principal: Almeida-Lousada, Hélder
Data de Publicação: 2021
Outros Autores: Mestre, André, Ramalhete, Sara Maria Ventura, Price, Aryeh J., De Mello, Ramon Andrade, Marreiros, Ana, Neves, Ricardo Pires das, Castelo-Branco, Pedro
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.1/17442
Resumo: Colorectal cancer (CRC) has an important bearing (top five) on cancer incidence and mortality in the world. The etiology of sporadic CRC is related to the accumulation of genetic and epigenetic alterations that result in the appearance of cancer hallmarks such as abnormal proliferation, evasion of immune destruction, resistance to apoptosis, replicative immortality, and others, contributing to cancer promotion, invasion, and metastasis. It is estimated that, each year, at least four million people are diagnosed with CRC in the world. Depending on CRC staging at diagnosis, many of these patients die, as CRC is in the top four causes of cancer death in the world. New and improved screening tests for CRC are needed to detect the disease at an early stage and adopt patient management strategies to decrease the death toll. The three pillars of CRC screening are endoscopy, radiological imaging, and molecular assays. Endoscopic procedures comprise traditional colonoscopy, and more recently, capsule-based endoscopy. The main imaging modality remains Computed Tomography (CT) of the colon. Molecular approaches continue to grow in the diversity of biomarkers and the sophistication of the technologies deployed to detect them. What started with simple fecal occult blood tests has expanded to an armamentarium, including mutation detection and identification of aberrant epigenetic signatures known to be oncogenic. Biomarker-based screening methods have critical advantages and are likely to eclipse the classical modalities of imaging and endoscopy in the future. For example, imaging methods are costly and require highly specialized medical personnel. In the case of endoscopy, their invasiveness limits compliance from large swaths of the population, especially those with average CRC risk. Beyond mere discomfort and fear, there are legitimate iatrogenic concerns associated with endoscopy. The risks of perforation and infection make endoscopy best suited for a confirmatory role in cases where there are positive results from other diagnostic tests. Biomarker-based screening methods are largely non-invasive and are growing in scope. Epigenetic biomarkers, in particular, can be detected in feces and blood, are less invasive to the average-risk patient, detect early-stage CRC, and have a demonstrably superior patient follow-up. Given the heterogeneity of CRC as it evolves, optimal screening may require a battery of blood and stool tests, where each can leverage different pathways perturbed during carcinogenesis. What follows is a comprehensive, systematic review of the literature pertaining to the screening and diagnostic protocols used in CRC. Relevant articles were retrieved from the PubMed database using keywords including: “Screening”, “Diagnosis”, and “Biomarkers for CRC”. American and European clinical trials in progress were included as well.
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spelling Screening for colorectal cancer leading into a new decade: the “Roaring ‘20s” for epigenetic biomarkers?Colorectal cancerEpigenetic testingScreeningDiagnosisCRC biomarkersColorectal cancer (CRC) has an important bearing (top five) on cancer incidence and mortality in the world. The etiology of sporadic CRC is related to the accumulation of genetic and epigenetic alterations that result in the appearance of cancer hallmarks such as abnormal proliferation, evasion of immune destruction, resistance to apoptosis, replicative immortality, and others, contributing to cancer promotion, invasion, and metastasis. It is estimated that, each year, at least four million people are diagnosed with CRC in the world. Depending on CRC staging at diagnosis, many of these patients die, as CRC is in the top four causes of cancer death in the world. New and improved screening tests for CRC are needed to detect the disease at an early stage and adopt patient management strategies to decrease the death toll. The three pillars of CRC screening are endoscopy, radiological imaging, and molecular assays. Endoscopic procedures comprise traditional colonoscopy, and more recently, capsule-based endoscopy. The main imaging modality remains Computed Tomography (CT) of the colon. Molecular approaches continue to grow in the diversity of biomarkers and the sophistication of the technologies deployed to detect them. What started with simple fecal occult blood tests has expanded to an armamentarium, including mutation detection and identification of aberrant epigenetic signatures known to be oncogenic. Biomarker-based screening methods have critical advantages and are likely to eclipse the classical modalities of imaging and endoscopy in the future. For example, imaging methods are costly and require highly specialized medical personnel. In the case of endoscopy, their invasiveness limits compliance from large swaths of the population, especially those with average CRC risk. Beyond mere discomfort and fear, there are legitimate iatrogenic concerns associated with endoscopy. The risks of perforation and infection make endoscopy best suited for a confirmatory role in cases where there are positive results from other diagnostic tests. Biomarker-based screening methods are largely non-invasive and are growing in scope. Epigenetic biomarkers, in particular, can be detected in feces and blood, are less invasive to the average-risk patient, detect early-stage CRC, and have a demonstrably superior patient follow-up. Given the heterogeneity of CRC as it evolves, optimal screening may require a battery of blood and stool tests, where each can leverage different pathways perturbed during carcinogenesis. What follows is a comprehensive, systematic review of the literature pertaining to the screening and diagnostic protocols used in CRC. Relevant articles were retrieved from the PubMed database using keywords including: “Screening”, “Diagnosis”, and “Biomarkers for CRC”. American and European clinical trials in progress were included as well.MDPISapientiaAlmeida-Lousada, HélderMestre, AndréRamalhete, Sara Maria VenturaPrice, Aryeh J.De Mello, Ramon AndradeMarreiros, AnaNeves, Ricardo Pires dasCastelo-Branco, Pedro2022-01-06T15:02:06Z2021-11-202021-12-23T15:06:31Z2021-11-20T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.1/17442engCurrent Oncology 28 (6): 4874-4893 (2021)1718-772910.3390/curroncol28060411info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-24T10:29:34Zoai:sapientia.ualg.pt:10400.1/17442Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:07:23.365543Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Screening for colorectal cancer leading into a new decade: the “Roaring ‘20s” for epigenetic biomarkers?
title Screening for colorectal cancer leading into a new decade: the “Roaring ‘20s” for epigenetic biomarkers?
spellingShingle Screening for colorectal cancer leading into a new decade: the “Roaring ‘20s” for epigenetic biomarkers?
Almeida-Lousada, Hélder
Colorectal cancer
Epigenetic testing
Screening
Diagnosis
CRC biomarkers
title_short Screening for colorectal cancer leading into a new decade: the “Roaring ‘20s” for epigenetic biomarkers?
title_full Screening for colorectal cancer leading into a new decade: the “Roaring ‘20s” for epigenetic biomarkers?
title_fullStr Screening for colorectal cancer leading into a new decade: the “Roaring ‘20s” for epigenetic biomarkers?
title_full_unstemmed Screening for colorectal cancer leading into a new decade: the “Roaring ‘20s” for epigenetic biomarkers?
title_sort Screening for colorectal cancer leading into a new decade: the “Roaring ‘20s” for epigenetic biomarkers?
author Almeida-Lousada, Hélder
author_facet Almeida-Lousada, Hélder
Mestre, André
Ramalhete, Sara Maria Ventura
Price, Aryeh J.
De Mello, Ramon Andrade
Marreiros, Ana
Neves, Ricardo Pires das
Castelo-Branco, Pedro
author_role author
author2 Mestre, André
Ramalhete, Sara Maria Ventura
Price, Aryeh J.
De Mello, Ramon Andrade
Marreiros, Ana
Neves, Ricardo Pires das
Castelo-Branco, Pedro
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Sapientia
dc.contributor.author.fl_str_mv Almeida-Lousada, Hélder
Mestre, André
Ramalhete, Sara Maria Ventura
Price, Aryeh J.
De Mello, Ramon Andrade
Marreiros, Ana
Neves, Ricardo Pires das
Castelo-Branco, Pedro
dc.subject.por.fl_str_mv Colorectal cancer
Epigenetic testing
Screening
Diagnosis
CRC biomarkers
topic Colorectal cancer
Epigenetic testing
Screening
Diagnosis
CRC biomarkers
description Colorectal cancer (CRC) has an important bearing (top five) on cancer incidence and mortality in the world. The etiology of sporadic CRC is related to the accumulation of genetic and epigenetic alterations that result in the appearance of cancer hallmarks such as abnormal proliferation, evasion of immune destruction, resistance to apoptosis, replicative immortality, and others, contributing to cancer promotion, invasion, and metastasis. It is estimated that, each year, at least four million people are diagnosed with CRC in the world. Depending on CRC staging at diagnosis, many of these patients die, as CRC is in the top four causes of cancer death in the world. New and improved screening tests for CRC are needed to detect the disease at an early stage and adopt patient management strategies to decrease the death toll. The three pillars of CRC screening are endoscopy, radiological imaging, and molecular assays. Endoscopic procedures comprise traditional colonoscopy, and more recently, capsule-based endoscopy. The main imaging modality remains Computed Tomography (CT) of the colon. Molecular approaches continue to grow in the diversity of biomarkers and the sophistication of the technologies deployed to detect them. What started with simple fecal occult blood tests has expanded to an armamentarium, including mutation detection and identification of aberrant epigenetic signatures known to be oncogenic. Biomarker-based screening methods have critical advantages and are likely to eclipse the classical modalities of imaging and endoscopy in the future. For example, imaging methods are costly and require highly specialized medical personnel. In the case of endoscopy, their invasiveness limits compliance from large swaths of the population, especially those with average CRC risk. Beyond mere discomfort and fear, there are legitimate iatrogenic concerns associated with endoscopy. The risks of perforation and infection make endoscopy best suited for a confirmatory role in cases where there are positive results from other diagnostic tests. Biomarker-based screening methods are largely non-invasive and are growing in scope. Epigenetic biomarkers, in particular, can be detected in feces and blood, are less invasive to the average-risk patient, detect early-stage CRC, and have a demonstrably superior patient follow-up. Given the heterogeneity of CRC as it evolves, optimal screening may require a battery of blood and stool tests, where each can leverage different pathways perturbed during carcinogenesis. What follows is a comprehensive, systematic review of the literature pertaining to the screening and diagnostic protocols used in CRC. Relevant articles were retrieved from the PubMed database using keywords including: “Screening”, “Diagnosis”, and “Biomarkers for CRC”. American and European clinical trials in progress were included as well.
publishDate 2021
dc.date.none.fl_str_mv 2021-11-20
2021-12-23T15:06:31Z
2021-11-20T00:00:00Z
2022-01-06T15:02:06Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.1/17442
url http://hdl.handle.net/10400.1/17442
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Current Oncology 28 (6): 4874-4893 (2021)
1718-7729
10.3390/curroncol28060411
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv MDPI
publisher.none.fl_str_mv MDPI
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