Circulating tumor DNA, liquid biopsy, and next generation sequencing: A comprehensive technical and clinical applications review

dc.contributor.authorAbou Daya, Sarah
dc.contributor.authorMahfouz, Rami A.R.
dc.contributor.departmentPathology and Laboratory Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:09:57Z
dc.date.available2025-01-24T12:09:57Z
dc.date.issued2018
dc.description.abstractCirculating tumor DNA (ctDNA) represents a small fraction of the total circulating free DNA and its analysis is increasingly used for diagnostic, prognostic and treatment purposes of cancer. ctDNA is released into the bloodstream from tumor cells through different mechanisms including apoptosis, necrosis, autophagy, and necroptosis. Liquid biopsy is a method used to detect specific cancer mutations in ctDNA from the plasma fraction of a standard blood draw and has numerous applications. Adoption of this newly introduced method has many advantages for detecting mutations in blood where it is an alternative to the direct sampling of tissue through resection and biopsy, as the genetic mutations present in a patient may change following treatment, and conducting additional biopsies and resection may present risk to the health status of the patient since it is an invasive technique. In addition, the information acquired from a single biopsy of a tumor is limited and might fail to reflect its heterogeneity, leading to a false negative reading, and finally, an alternative to direct tissue sampling may also lessen the fiduciary and resource strain on caregivers and patients. Next Generation Sequencing (NGS) is gaining more presence in diagnostic molecular laboratories and is nowadays very close to embrace the field of liquid biopsies with an ultimate sensitivity and range of clinical applications. This review article is a first comprehensive technical overview of the ctDNA detection using NGS as a state-of-the-art technology. © 2018 Elsevier B.V.
dc.identifier.doihttps://doi.org/10.1016/j.mgene.2018.06.013
dc.identifier.eid2-s2.0-85048959583
dc.identifier.urihttp://hdl.handle.net/10938/32198
dc.language.isoen
dc.publisherElsevier B.V.
dc.relation.ispartofMeta Gene
dc.sourceScopus
dc.subjectCtdna
dc.subjectNgs
dc.subjectReview
dc.subjectBiological marker
dc.subjectCirculating tumor dna
dc.subjectEpidermal growth factor receptor
dc.subjectGefitinib
dc.subjectTrastuzumab
dc.subjectAcute myeloid leukemia
dc.subjectApoptosis
dc.subjectAutophagy
dc.subjectBone marrow biopsy
dc.subjectCancer growth
dc.subjectCaregiver
dc.subjectCirculating tumor cell
dc.subjectColorectal cancer
dc.subjectCopy number variation
dc.subjectDiagnostic test accuracy study
dc.subjectDna extraction
dc.subjectDna sequence
dc.subjectFluorescence in situ hybridization
dc.subjectGene amplification
dc.subjectGene mutation
dc.subjectGene sequence
dc.subjectGenetic analysis
dc.subjectHigh throughput sequencing
dc.subjectHuman
dc.subjectLiquid biopsy
dc.subjectMalignant neoplasms subdivided by anatomical site
dc.subjectMinimal residual disease
dc.subjectNecroptosis
dc.subjectNecrosis
dc.subjectNext generation sequencing
dc.subjectOncogene c myc
dc.subjectOverall survival
dc.subjectPancreas adenocarcinoma
dc.subjectPolymerase chain reaction
dc.subjectPredictive value
dc.subjectPriority journal
dc.subjectReverse transcription polymerase chain reaction
dc.subjectSensitivity and specificity
dc.subjectSingle nucleotide polymorphism
dc.subjectSomatic mutation
dc.subjectThyroid papillary carcinoma
dc.subjectTreatment response
dc.subjectTriple negative breast cancer
dc.subjectTumor suppressor gene
dc.subjectTumor volume
dc.subjectUpregulation
dc.titleCirculating tumor DNA, liquid biopsy, and next generation sequencing: A comprehensive technical and clinical applications review
dc.typeReview

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