Liquid biopsy approach to pancreatic cancer.

dc.contributor.authorPerales, Sonia
dc.contributor.authorTorres, Carolina
dc.contributor.authorJimenez-Luna, Cristina
dc.contributor.authorPrados, Jose
dc.contributor.authorMartinez-Galan, Joaquina
dc.contributor.authorSanchez-Manas, Jose Manuel
dc.contributor.authorCaba, Octavio
dc.date.accessioned2025-01-07T14:22:35Z
dc.date.available2025-01-07T14:22:35Z
dc.date.issued2021
dc.description.abstractPancreatic cancer (PC) continues to pose a major clinical challenge. There has been little improvement in patient survival over the past few decades, and it is projected to become the second leading cause of cancer mortality by 2030. The dismal 5-year survival rate of less than 10% after the diagnosis is attributable to the lack of early symptoms, the absence of specific biomarkers for an early diagnosis, and the inadequacy of available chemotherapies. Most patients are diagnosed when the disease has already metastasized and cannot be treated. Cancer interception is vital, actively intervening in the malignization process before the development of a full-blown advanced tumor. An early diagnosis of PC has a dramatic impact on the survival of patients, and improved techniques are urgently needed to detect and evaluate this disease at an early stage. It is difficult to obtain tissue biopsies from the pancreas due to its anatomical position; however, liquid biopsies are readily available and can provide useful information for the diagnosis, prognosis, stratification, and follow-up of patients with PC and for the design of individually tailored treatments. The aim of this review was to provide an update of the latest advances in knowledge on the application of carbohydrates, proteins, cell-free nucleic acids, circulating tumor cells, metabolome compounds, exosomes, and platelets in blood as potential biomarkers for PC, focusing on their clinical relevance and potential for improving patient outcomes.
dc.identifier.doi10.4251/wjgo.v13.i10.1263
dc.identifier.issn1948-5204
dc.identifier.pmcPMC8529923
dc.identifier.pmid34721766
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC8529923/pdf
dc.identifier.unpaywallURLhttps://doi.org/10.4251/wjgo.v13.i10.1263
dc.identifier.urihttps://hdl.handle.net/10668/26330
dc.issue.number10
dc.journal.titleWorld journal of gastrointestinal oncology
dc.journal.titleabbreviationWorld J Gastrointest Oncol
dc.language.isoen
dc.organizationSAS - Hospital Universitario Virgen de las Nieves
dc.page.number1263-1287
dc.pubmedtypeJournal Article
dc.pubmedtypeReview
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectBiomarkers
dc.subjectCancer interception
dc.subjectCancer monitoring
dc.subjectClinical management
dc.subjectLiquid biopsy
dc.subjectPancreatic cancer
dc.titleLiquid biopsy approach to pancreatic cancer.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number13

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