Translating Biomarkers of Cholangiocarcinoma for Theranosis: A Systematic Review
Cholangiocarcinoma (CCA) is a rare disease with poor outcomes and limited research efforts into novel treatment options. A systematic review of CCA biomarkers was undertaken to identify promising biomarkers that may be used for theranosis (therapy and diagnosis). MEDLINE/EMBASE databases (1996-2019)...
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Published in | Cancers Vol. 12; no. 10; p. 2817 |
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Language | English |
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Abstract | Cholangiocarcinoma (CCA) is a rare disease with poor outcomes and limited research efforts into novel treatment options. A systematic review of CCA biomarkers was undertaken to identify promising biomarkers that may be used for theranosis (therapy and diagnosis). MEDLINE/EMBASE databases (1996-2019) were systematically searched using two strategies to identify biomarker studies of CCA. The PANTHER Go-Slim classification system and STRING network version 11.0 were used to interrogate the identified biomarkers. The TArget Selection Criteria for Theranosis (TASC-T) score was used to rank identified proteins as potential targetable biomarkers for theranosis. The following proteins scored the highest, CA9, CLDN18, TNC, MMP9, and EGFR, and they were evaluated in detail. None of these biomarkers had high sensitivity or specificity for CCA but have potential for theranosis. This review is unique in that it describes the process of selecting suitable markers for theranosis, which is also applicable to other diseases. This has highlighted existing validated markers of CCA that can be used for active tumor targeting for the future development of targeted theranostic delivery systems. It also emphasizes the relevance of bioinformatics in aiding the search for validated biomarkers that could be repurposed for theranosis. |
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AbstractList | Cholangiocarcinoma (CCA) is a rare disease with poor outcomes and limited research efforts into novel treatment options. A systematic review of CCA biomarkers was undertaken to identify promising biomarkers that may be used for theranosis (therapy and diagnosis). MEDLINE/EMBASE databases (1996-2019) were systematically searched using two strategies to identify biomarker studies of CCA. The PANTHER Go-Slim classification system and STRING network version 11.0 were used to interrogate the identified biomarkers. The TArget Selection Criteria for Theranosis (TASC-T) score was used to rank identified proteins as potential targetable biomarkers for theranosis. The following proteins scored the highest, CA9, CLDN18, TNC, MMP9, and EGFR, and they were evaluated in detail. None of these biomarkers had high sensitivity or specificity for CCA but have potential for theranosis. This review is unique in that it describes the process of selecting suitable markers for theranosis, which is also applicable to other diseases. This has highlighted existing validated markers of CCA that can be used for active tumor targeting for the future development of targeted theranostic delivery systems. It also emphasizes the relevance of bioinformatics in aiding the search for validated biomarkers that could be repurposed for theranosis. Bile duct cancers are rare cancers that have poor prospects and limited treatment options. Recently, significant advances have been made in the field of nanomedicine which has allowed new approaches to the diagnosis and treatment (i.e., theranosis) of human diseases. To develop nanomedicines that could earmark or target bile duct cancer, specific proteins (or biomarkers) that are present in bile duct cancer but absent in normal tissues are required. We conducted a systematic search of the published literature for bile duct cancer biomarkers that would be suitable for theranosis. Specialist bioinformatics tools were used to help categorize the resulting data set. To select the most promising biomarkers from the search, biomarkers were ranked according to a theranosis-scoring-system and then evaluated in detail. The biomarkers identified using this approach have the potential to promote targeted nanomedicine-based systems to treat bile duct cancers. Cholangiocarcinoma (CCA) is a rare disease with poor outcomes and limited research efforts into novel treatment options. A systematic review of CCA biomarkers was undertaken to identify promising biomarkers that may be used for theranosis (therapy and diagnosis). MEDLINE/EMBASE databases (1996-2019) were systematically searched using two strategies to identify biomarker studies of CCA. The PANTHER Go-Slim classification system and STRING network version 11.0 were used to interrogate the identified biomarkers. The TArget Selection Criteria for Theranosis (TASC-T) score was used to rank identified proteins as potential targetable biomarkers for theranosis. The following proteins scored the highest, CA9, CLDN18, TNC, MMP9, and EGFR, and they were evaluated in detail. None of these biomarkers had high sensitivity or specificity for CCA but have potential for theranosis. This review is unique in that it describes the process of selecting suitable markers for theranosis, which is also applicable to other diseases. This has highlighted existing validated markers of CCA that can be used for active tumor targeting for the future development of targeted theranostic delivery systems. It also emphasizes the relevance of bioinformatics in aiding the search for validated biomarkers that could be repurposed for theranosis.Cholangiocarcinoma (CCA) is a rare disease with poor outcomes and limited research efforts into novel treatment options. A systematic review of CCA biomarkers was undertaken to identify promising biomarkers that may be used for theranosis (therapy and diagnosis). MEDLINE/EMBASE databases (1996-2019) were systematically searched using two strategies to identify biomarker studies of CCA. The PANTHER Go-Slim classification system and STRING network version 11.0 were used to interrogate the identified biomarkers. The TArget Selection Criteria for Theranosis (TASC-T) score was used to rank identified proteins as potential targetable biomarkers for theranosis. The following proteins scored the highest, CA9, CLDN18, TNC, MMP9, and EGFR, and they were evaluated in detail. None of these biomarkers had high sensitivity or specificity for CCA but have potential for theranosis. This review is unique in that it describes the process of selecting suitable markers for theranosis, which is also applicable to other diseases. This has highlighted existing validated markers of CCA that can be used for active tumor targeting for the future development of targeted theranostic delivery systems. It also emphasizes the relevance of bioinformatics in aiding the search for validated biomarkers that could be repurposed for theranosis. Simple SummaryBile duct cancers are rare cancers that have poor prospects and limited treatment options. Recently, significant advances have been made in the field of nanomedicine which has allowed new approaches to the diagnosis and treatment (i.e., theranosis) of human diseases. To develop nanomedicines that could earmark or target bile duct cancer, specific proteins (or biomarkers) that are present in bile duct cancer but absent in normal tissues are required. We conducted a systematic search of the published literature for bile duct cancer biomarkers that would be suitable for theranosis. Specialist bioinformatics tools were used to help categorize the resulting data set. To select the most promising biomarkers from the search, biomarkers were ranked according to a theranosis-scoring-system and then evaluated in detail. The biomarkers identified using this approach have the potential to promote targeted nanomedicine-based systems to treat bile duct cancers.AbstractCholangiocarcinoma (CCA) is a rare disease with poor outcomes and limited research efforts into novel treatment options. A systematic review of CCA biomarkers was undertaken to identify promising biomarkers that may be used for theranosis (therapy and diagnosis). MEDLINE/EMBASE databases (1996–2019) were systematically searched using two strategies to identify biomarker studies of CCA. The PANTHER Go-Slim classification system and STRING network version 11.0 were used to interrogate the identified biomarkers. The TArget Selection Criteria for Theranosis (TASC-T) score was used to rank identified proteins as potential targetable biomarkers for theranosis. The following proteins scored the highest, CA9, CLDN18, TNC, MMP9, and EGFR, and they were evaluated in detail. None of these biomarkers had high sensitivity or specificity for CCA but have potential for theranosis. This review is unique in that it describes the process of selecting suitable markers for theranosis, which is also applicable to other diseases. This has highlighted existing validated markers of CCA that can be used for active tumor targeting for the future development of targeted theranostic delivery systems. It also emphasizes the relevance of bioinformatics in aiding the search for validated biomarkers that could be repurposed for theranosis. |
Audience | Academic |
Author | Charalambous, Antonia Nair, Amit Ingram, Nicola Wijetunga, Imeshi Coletta, P Louise McVeigh, Laura E Carr, Ian M Antanaviciute, Agne Prasad, K Raj |
AuthorAffiliation | 2 Department of Hepatobiliary and Transplant Surgery, St. James’s University Hospital, Leeds LS9 7TF, UK; raj.prasad@nhs.net 1 Leeds Institute of Medical Research, Wellcome Trust Brenner Building, St James’s University Hospital, Leeds LS9 7TF, UK; i.wijetunga@nhs.net (I.W.); 20mcveigh@gmail.com (L.E.M.); antonia.charalambous11@gmail.com (A.C.); agne.antanaviciute@ndm.ox.ac.uk (A.A.); i.m.carr@leeds.ac.uk (I.M.C.); nair.amit@doctors.org.uk (A.N.); n.ingram@leeds.ac.uk (N.I.) |
AuthorAffiliation_xml | – name: 2 Department of Hepatobiliary and Transplant Surgery, St. James’s University Hospital, Leeds LS9 7TF, UK; raj.prasad@nhs.net – name: 1 Leeds Institute of Medical Research, Wellcome Trust Brenner Building, St James’s University Hospital, Leeds LS9 7TF, UK; i.wijetunga@nhs.net (I.W.); 20mcveigh@gmail.com (L.E.M.); antonia.charalambous11@gmail.com (A.C.); agne.antanaviciute@ndm.ox.ac.uk (A.A.); i.m.carr@leeds.ac.uk (I.M.C.); nair.amit@doctors.org.uk (A.N.); n.ingram@leeds.ac.uk (N.I.) |
Author_xml | – sequence: 1 givenname: Imeshi orcidid: 0000-0002-4128-7381 surname: Wijetunga fullname: Wijetunga, Imeshi organization: Leeds Institute of Medical Research, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, UK – sequence: 2 givenname: Laura E orcidid: 0000-0001-9417-8632 surname: McVeigh fullname: McVeigh, Laura E organization: Leeds Institute of Medical Research, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, UK – sequence: 3 givenname: Antonia orcidid: 0000-0001-5895-3697 surname: Charalambous fullname: Charalambous, Antonia organization: Leeds Institute of Medical Research, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, UK – sequence: 4 givenname: Agne surname: Antanaviciute fullname: Antanaviciute, Agne organization: Leeds Institute of Medical Research, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, UK – sequence: 5 givenname: Ian M orcidid: 0000-0001-9544-1068 surname: Carr fullname: Carr, Ian M organization: Leeds Institute of Medical Research, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, UK – sequence: 6 givenname: Amit orcidid: 0000-0003-1344-392X surname: Nair fullname: Nair, Amit organization: Leeds Institute of Medical Research, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, UK – sequence: 7 givenname: K Raj surname: Prasad fullname: Prasad, K Raj organization: Department of Hepatobiliary and Transplant Surgery, St. James's University Hospital, Leeds LS9 7TF, UK – sequence: 8 givenname: Nicola surname: Ingram fullname: Ingram, Nicola organization: Leeds Institute of Medical Research, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, UK – sequence: 9 givenname: P Louise surname: Coletta fullname: Coletta, P Louise organization: Leeds Institute of Medical Research, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, UK |
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CitedBy_id | crossref_primary_10_3389_fchem_2021_699284 crossref_primary_10_3390_cancers13040919 crossref_primary_10_1177_00031348221124323 crossref_primary_10_3389_fgene_2022_868015 |
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Keywords | therapy and diagnosis theranosis cholangiocarcinoma biomarkers biomarker selection |
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Snippet | Cholangiocarcinoma (CCA) is a rare disease with poor outcomes and limited research efforts into novel treatment options. A systematic review of CCA biomarkers... Bile duct cancers are rare cancers that have poor prospects and limited treatment options. Recently, significant advances have been made in the field of... Simple SummaryBile duct cancers are rare cancers that have poor prospects and limited treatment options. Recently, significant advances have been made in the... |
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SourceType | Open Access Repository Aggregation Database Index Database |
StartPage | 2817 |
SubjectTerms | Bile ducts Bioinformatics Biomarkers Cancer Cancer therapies Cholangiocarcinoma Diagnosis Disease Gelatinase B Genes Genetic translation Growth factors Health aspects Medical prognosis Nanoparticles Nanotechnology Ontology Proteins Rare diseases Review Reviews Systematic review |
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Title | Translating Biomarkers of Cholangiocarcinoma for Theranosis: A Systematic Review |
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