4.5 Review

Antibodies as biomarkers for cancer risk: a systematic review

Journal

CLINICAL AND EXPERIMENTAL IMMUNOLOGY
Volume 209, Issue 1, Pages 46-63

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/cei/uxac030

Keywords

antibodies; biomarkers; cancer; early detection; tumor -associated antigens; immunoglobulin

Categories

Funding

  1. National Institute for Health Research (NIHR) Biomedical Research Centre (BRC) based at Guy's and St Thomas' NHS Foundation Trust and King's College London [IS-BRC-1215-20006]

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The humoral immune response is closely associated with the development of cancer, and antibodies have been found to have predictive value in assessing site-specific cancer risk. Different types of antibodies, especially immunoglobulin isotypes, tumor-associated antigen-specific, and self-reactive antibodies, are linked to cancer risk.
The humoral immune response has been consistently linked with the development of various cancers. Therefore, increasing evidence has investigated the predictive value of antibodies to assess site-specific cancer risk. In the current study, we review the current evidence for the association between the most researched antibodies and risk of site-specific cancers Increasing evidence has linked the humoral immune response with the development of various cancers. Therefore, there is growing interest in investigating the predictive value of antibodies to assess overall and tissue site-specific cancer risk. Given the large amount of antibody types and the broad scope of the search (i.e. cancer risk), the primary aim of this systematic review was to present an overview of the most researched antibodies (i.e. immunoglobulin (Ig) isotypes (IgG, IgM, IgA, and IgE), tumour and self-antigen-reactive antibodies, infection-related antibodies) in relation to overall and site-specific cancer risk. We identified various antibody types that have been associated with the risk of cancer. While no significant associations were found for IgM serum levels, studies found an inconsistent association among IgE, IgA, and IgG serum levels in relation to cancer risk. When evaluating antibodies against infectious agents, most studies reported a positive link with specific cancers known to be associated with the specific agent recognized by serum antibodies (i.e. helicobacter pylori and gastric cancer, hepatitis B virus and hepatocellular carcinoma, and human papillomavirus and cervical cancer). Several reports identified autoantibodies, as single biomarkers (e.g. anti-p53, anti-MUC1, and anti-CA125) but especially in panels of multiple autoantibodies, to have potential as diagnostic biomarkers for specific cancer types. Overall, there is emerging evidence associating certain antibodies to cancer risk, especially immunoglobulin isotypes, tumour-associated antigen-specific, and self-reactive antibodies. Further experimental studies are necessary to assess the efficacy of specific antibodies as markers for the early diagnosis of cancer.

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