Liquid biopsy derived circulating tumor cells and circulating tumor DNA as novel biomarkers in hepatocellular carcinoma

dc.contributor.authorTemraz, Sally N.
dc.contributor.authorNasr, Rihab R.
dc.contributor.authorMukherji, Deborah M.
dc.contributor.authorKreidieh, Firas Y.
dc.contributor.authorShamseddine, Ali I.
dc.contributor.departmentInternal Medicine
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:44:43Z
dc.date.available2025-01-24T11:44:43Z
dc.date.issued2022
dc.description.abstractIntroduction: The diagnosis of hepatocellular carcinoma (HCC) is made at a relatively advanced stage resulting in poor prognosis. Alpha-fetoprotein and liver ultrasound have limited accuracy as biomarkers in HCC. Liver biopsy provides information on tumor biology; however, it is invasive and holds high threat of tumor seeding. Thus, more accurate and less invasive approaches are needed Areas Covered: Highly sensitive liquid biopsy assays have made possible the detection and analysis of cells or organelles such as circulating tumor cells (CTCs), circulating tumor DNA (ctDNA), and tumor-derived exosomes. Here, we focus on CTCs and ctDNA components of liquid biopsy and their clinical application as diagnostic, prognostic, and predictive biomarkers in HCC. Unlike tissue biopsy, liquid biopsy involves attaining a sample at several time frames in an easy and a non-invasive manner. They have been efficacious in detecting and classifying cancer, in predicting treatment response, in monitoring disease relapse and in identifying mechanisms of resistance to targeted therapies. Expert Opinion: Although interesting and highly promising, liquid biopsy techniques still have many obstacles to overcome before their wide spread clinical application sees the light. It is expected that these techniques will be incorporated into traditional methodologies for better diagnostic, predictive and prognostic results. © 2022 Informa UK Limited, trading as Taylor & Francis Group.
dc.identifier.doihttps://doi.org/10.1080/14737159.2022.2094706
dc.identifier.eid2-s2.0-85133192949
dc.identifier.pmid35758097
dc.identifier.urihttp://hdl.handle.net/10938/30484
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofExpert Review of Molecular Diagnostics
dc.sourceScopus
dc.subjectBiomarker
dc.subjectClinical implication
dc.subjectCtc
dc.subjectCtdna
dc.subjectHepatocellular carcinoma
dc.subjectLiquid biopsy
dc.subjectBiomarkers, tumor
dc.subjectCarcinoma, hepatocellular
dc.subjectCirculating tumor dna
dc.subjectHumans
dc.subjectLiver neoplasms
dc.subjectNeoplastic cells, circulating
dc.subjectBiological marker
dc.subjectTumor marker
dc.subjectCancer growth
dc.subjectCancer prognosis
dc.subjectCancer recurrence
dc.subjectCell organelle
dc.subjectCirculating tumor cell
dc.subjectClinical decision making
dc.subjectHuman
dc.subjectLiver cell carcinoma
dc.subjectMolecularly targeted therapy
dc.subjectRelapse
dc.subjectReview
dc.subjectSingle cell analysis
dc.subjectSurgical technique
dc.subjectTranscriptomics
dc.subjectTreatment response
dc.subjectGenetics
dc.subjectLiver tumor
dc.subjectPathology
dc.subjectProcedures
dc.subjectTumor embolism
dc.titleLiquid biopsy derived circulating tumor cells and circulating tumor DNA as novel biomarkers in hepatocellular carcinoma
dc.typeReview

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