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Biomarker Reproducibility Challenge: A Review of Non-Nucleotide Biomarker Discovery Protocols from Body Fluids in Breast Cancer Diagnosis

SIMPLE SUMMARY: Various studies and techniques have been designed to discover biofluid-derived biomarkers for non-invasive early detection and prognosis of cancers. Despite the importance of non-invasive biomarker discovery in cancer diagnosis and management, the reported markers are often inconsist...

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Autores principales: Safari, Fatemeh, Kehelpannala, Cheka, Safarchi, Azadeh, Batarseh, Amani M., Vafaee, Fatemeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216598/
https://www.ncbi.nlm.nih.gov/pubmed/37345117
http://dx.doi.org/10.3390/cancers15102780
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author Safari, Fatemeh
Kehelpannala, Cheka
Safarchi, Azadeh
Batarseh, Amani M.
Vafaee, Fatemeh
author_facet Safari, Fatemeh
Kehelpannala, Cheka
Safarchi, Azadeh
Batarseh, Amani M.
Vafaee, Fatemeh
author_sort Safari, Fatemeh
collection PubMed
description SIMPLE SUMMARY: Various studies and techniques have been designed to discover biofluid-derived biomarkers for non-invasive early detection and prognosis of cancers. Despite the importance of non-invasive biomarker discovery in cancer diagnosis and management, the reported markers are often inconsistent and irreproducible across different studies and cohorts. In this article, we reviewed the ongoing trend of non-nucleotide biomarkers, including lipidomics, proteomics and metabolomics, derived from body fluids, with a focus on breast cancer, and reviewed the inconstancies in the biomarker discovery pipelines across pre-analytical, analytical, and post-analytical phases, covering the diversity of approaches from sample processing to predictive modelling and validation. ABSTRACT: Breast cancer has now become the most commonly diagnosed cancer, accounting for one in eight cancer diagnoses worldwide. Non-invasive diagnostic biomarkers and associated tests are superlative candidates to complement or improve current approaches for screening, early diagnosis, or prognosis of breast cancer. Biomarkers detected from body fluids such as blood (serum/plasma), urine, saliva, nipple aspiration fluid, and tears can detect breast cancer at its early stages in a minimally invasive way. The advancements in high-throughput molecular profiling (omics) technologies have opened an unprecedented opportunity for unbiased biomarker detection. However, the irreproducibility of biomarkers and discrepancies of reported markers have remained a major roadblock to clinical implementation, demanding the investigation of contributing factors and the development of standardised biomarker discovery pipelines. A typical biomarker discovery workflow includes pre-analytical, analytical, and post-analytical phases, from sample collection to model development. Variations introduced during these steps impact the data quality and the reproducibility of the findings. Here, we present a comprehensive review of methodological variations in biomarker discovery studies in breast cancer, with a focus on non-nucleotide biomarkers (i.e., proteins, lipids, and metabolites), highlighting the pre-analytical to post-analytical variables, which may affect the accurate identification of biomarkers from body fluids.
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spelling pubmed-102165982023-05-27 Biomarker Reproducibility Challenge: A Review of Non-Nucleotide Biomarker Discovery Protocols from Body Fluids in Breast Cancer Diagnosis Safari, Fatemeh Kehelpannala, Cheka Safarchi, Azadeh Batarseh, Amani M. Vafaee, Fatemeh Cancers (Basel) Review SIMPLE SUMMARY: Various studies and techniques have been designed to discover biofluid-derived biomarkers for non-invasive early detection and prognosis of cancers. Despite the importance of non-invasive biomarker discovery in cancer diagnosis and management, the reported markers are often inconsistent and irreproducible across different studies and cohorts. In this article, we reviewed the ongoing trend of non-nucleotide biomarkers, including lipidomics, proteomics and metabolomics, derived from body fluids, with a focus on breast cancer, and reviewed the inconstancies in the biomarker discovery pipelines across pre-analytical, analytical, and post-analytical phases, covering the diversity of approaches from sample processing to predictive modelling and validation. ABSTRACT: Breast cancer has now become the most commonly diagnosed cancer, accounting for one in eight cancer diagnoses worldwide. Non-invasive diagnostic biomarkers and associated tests are superlative candidates to complement or improve current approaches for screening, early diagnosis, or prognosis of breast cancer. Biomarkers detected from body fluids such as blood (serum/plasma), urine, saliva, nipple aspiration fluid, and tears can detect breast cancer at its early stages in a minimally invasive way. The advancements in high-throughput molecular profiling (omics) technologies have opened an unprecedented opportunity for unbiased biomarker detection. However, the irreproducibility of biomarkers and discrepancies of reported markers have remained a major roadblock to clinical implementation, demanding the investigation of contributing factors and the development of standardised biomarker discovery pipelines. A typical biomarker discovery workflow includes pre-analytical, analytical, and post-analytical phases, from sample collection to model development. Variations introduced during these steps impact the data quality and the reproducibility of the findings. Here, we present a comprehensive review of methodological variations in biomarker discovery studies in breast cancer, with a focus on non-nucleotide biomarkers (i.e., proteins, lipids, and metabolites), highlighting the pre-analytical to post-analytical variables, which may affect the accurate identification of biomarkers from body fluids. MDPI 2023-05-16 /pmc/articles/PMC10216598/ /pubmed/37345117 http://dx.doi.org/10.3390/cancers15102780 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Safari, Fatemeh
Kehelpannala, Cheka
Safarchi, Azadeh
Batarseh, Amani M.
Vafaee, Fatemeh
Biomarker Reproducibility Challenge: A Review of Non-Nucleotide Biomarker Discovery Protocols from Body Fluids in Breast Cancer Diagnosis
title Biomarker Reproducibility Challenge: A Review of Non-Nucleotide Biomarker Discovery Protocols from Body Fluids in Breast Cancer Diagnosis
title_full Biomarker Reproducibility Challenge: A Review of Non-Nucleotide Biomarker Discovery Protocols from Body Fluids in Breast Cancer Diagnosis
title_fullStr Biomarker Reproducibility Challenge: A Review of Non-Nucleotide Biomarker Discovery Protocols from Body Fluids in Breast Cancer Diagnosis
title_full_unstemmed Biomarker Reproducibility Challenge: A Review of Non-Nucleotide Biomarker Discovery Protocols from Body Fluids in Breast Cancer Diagnosis
title_short Biomarker Reproducibility Challenge: A Review of Non-Nucleotide Biomarker Discovery Protocols from Body Fluids in Breast Cancer Diagnosis
title_sort biomarker reproducibility challenge: a review of non-nucleotide biomarker discovery protocols from body fluids in breast cancer diagnosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216598/
https://www.ncbi.nlm.nih.gov/pubmed/37345117
http://dx.doi.org/10.3390/cancers15102780
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