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Cho, Yoon-Kyoung
FRUITS Lab.
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dc.citation.number 6 -
dc.citation.startPage e0180251 -
dc.citation.title PLOS ONE -
dc.citation.volume 12 -
dc.contributor.author Kang, Hwa Mi -
dc.contributor.author Kim, Gwang Ha -
dc.contributor.author Jeon, Hye Kyung -
dc.contributor.author Kim, Dae Hwan -
dc.contributor.author Jeon, Tae Yong -
dc.contributor.author Park, Do Youn -
dc.contributor.author Jeong, Hyunjin -
dc.contributor.author Chun, Won Joo -
dc.contributor.author Kim, Mi-Hyun -
dc.contributor.author Park, Juhee -
dc.contributor.author Lim, Minji -
dc.contributor.author Kim, Tae-Hyeong -
dc.contributor.author Cho, Yoon-Kyung -
dc.date.accessioned 2023-12-21T22:10:22Z -
dc.date.available 2023-12-21T22:10:22Z -
dc.date.created 2017-07-31 -
dc.date.issued 2017-06 -
dc.description.abstract [Background] The use of circulating tumor cells (CTCs) as an early diagnostic biomarker and prognostic indicator after surgery or chemotherapy has been suggested for various cancers. This study aimed to evaluate CTCs in patients who underwent gastrectomy for gastric cancer and to explore their clinical usefulness in the early diagnosis of gastric cancer.
[Methods] A total of 116 patients with gastric cancer who underwent gastrectomy and 31 healthy volunteers were prospectively included between 2014 and 2015. Peripheral blood samples were collected before gastrectomy, and CTCs were examined using a centrifugal microfluidic system with a new fluid-assisted separation technique.
[Results] After creating a receiver operating characteristic curve to identify the discriminative CTC value needed differentiate patients with gastric cancer from healthy volunteers, sensitivity and specificity were nearly optimized at a CTC threshold of 2 per 7.5 mL of blood. Of the 102 persons with a CTC level >= 2 per 7.5 mL of blood, 99 (97.1%) had gastric cancer, and of the 45 persons with a CTC level <2 per 7.5 mL of blood, 28 (62.2%) were healthy controls. Accordingly, the sensitivity and specificity for the differentiation of patients with gastric cancer from healthy controls were 85.3% and 90.3%, respectively. However, the presence of CTCs was not associated with any clinicopathologic features such as staging, histologic type, or mucin phenotype.
[Conclusion] Although we could not prove the clinical feasibility of CTCs for gastric cancer staging, our results suggest a potential role of CTCs as an early diagnostic biomarker of gastric cancer.
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dc.identifier.bibliographicCitation PLOS ONE, v.12, no.6, pp.e0180251 -
dc.identifier.doi 10.1371/journal.pone.0180251 -
dc.identifier.issn 1932-6203 -
dc.identifier.scopusid 2-s2.0-85021660019 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/22443 -
dc.identifier.url http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0180251 -
dc.identifier.wosid 000404608300132 -
dc.language 영어 -
dc.publisher PUBLIC LIBRARY SCIENCE -
dc.title Circulating tumor cells detected by lab-on-adisc: Role in early diagnosis of gastric cancer -
dc.type Article -
dc.description.isOpenAccess TRUE -
dc.relation.journalWebOfScienceCategory Multidisciplinary Sciences -
dc.relation.journalResearchArea Science & Technology - Other Topics -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus PROGNOSTIC-SIGNIFICANCE -
dc.subject.keywordPlus MICROFLUIDIC DEVICE -
dc.subject.keywordPlus PERIPHERAL-BLOOD -
dc.subject.keywordPlus CLINICAL-SIGNIFICANCE -
dc.subject.keywordPlus MOLECULAR-DETECTION -
dc.subject.keywordPlus MUCIN EXPRESSION -
dc.subject.keywordPlus HIGH-PURITY -
dc.subject.keywordPlus ENRICHMENT -
dc.subject.keywordPlus METASTASIS -
dc.subject.keywordPlus CARCINOMAS -

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