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Plasma MicroRNA-21, 26a, and 29a-3p as Predictive Markers for Treatment Response Following Transarterial Chemoembolization in Patients with Hepatocellular Carcinoma
DC Field | Value | Language |
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dc.contributor.author | Kim, SS | - |
dc.contributor.author | Cho, HJ | - |
dc.contributor.author | Nam, JS | - |
dc.contributor.author | Kim, HJ | - |
dc.contributor.author | Kang, DR | - |
dc.contributor.author | Won, JH | - |
dc.contributor.author | Kim, J | - |
dc.contributor.author | Kim, JK | - |
dc.contributor.author | Lee, JH | - |
dc.contributor.author | Kim, BH | - |
dc.contributor.author | Lee, MY | - |
dc.contributor.author | Cho, SW | - |
dc.contributor.author | Cheong, JY | - |
dc.date.accessioned | 2019-11-13T00:17:20Z | - |
dc.date.available | 2019-11-13T00:17:20Z | - |
dc.date.issued | 2018 | - |
dc.identifier.issn | 1011-8934 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/16652 | - |
dc.description.abstract | BACKGROUND: We investigated an association between the levels of plasma microRNA (miRNA)-21, -26a, and -29a-3p and treatment outcomes following transarterial chemoembolization (TACE) in patients with hepatocellular carcinoma (HCC).
METHODS: A total of 198 patients with TACE-treated HCC were followed up for TACE refractoriness and liver transplantation (LT)-free survival. Pretreatment plasma miRNA-21, -26a, and -29a-3p levels were measured using quantitative real-time polymerase chain reaction. RESULTS: During the mean follow-up of 22.3 (range, 0.7-79) months, 118 (59.6%) patients exhibited TACE refractoriness. Multivariate analyses showed that expression of a specific combination of miRNAs (miRNA-21 >/= 2.5, miRNA-26a >/= 1.5, and miRNA-29a-3p < 0.4) was associated with early TACE refractoriness (within 1 year: hazard ratio [HR], 2.32: 95% confidence interval [CI], 1.08-4.99: P = 0.031) together with tumor size (HR, 4.62: 95% CI, 1.50-14.21: P = 0.008), and macrovascular invasion (HR, 3.80: 95% CI, 1.19-12.20: P = 0.025). However, miRNA-21, -26a, and -29a-3p levels were not significantly associated with overall TACE refractoriness or LT-free survival. Additionally, large tumor size and macrovascular invasion were common predictive factor of overall TACE refractoriness and survival. CONCLUSION: Combination of plasma miRNA-21, -26a, and -29a-3p expression could predict early TACE refractoriness in patients with TACE-treated HCC. | - |
dc.language.iso | en | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Area Under Curve | - |
dc.subject.MESH | Carcinoma, Hepatocellular | - |
dc.subject.MESH | Chemoembolization, Therapeutic | - |
dc.subject.MESH | Doxorubicin | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Liver Neoplasms | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | MicroRNAs | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Neoplasm Staging | - |
dc.subject.MESH | Proportional Hazards Models | - |
dc.subject.MESH | ROC Curve | - |
dc.subject.MESH | Real-Time Polymerase Chain Reaction | - |
dc.subject.MESH | Survival Rate | - |
dc.title | Plasma MicroRNA-21, 26a, and 29a-3p as Predictive Markers for Treatment Response Following Transarterial Chemoembolization in Patients with Hepatocellular Carcinoma | - |
dc.type | Article | - |
dc.identifier.pmid | 29215815 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729641/ | - |
dc.subject.keyword | Chemoembolization, Therapeutic | - |
dc.subject.keyword | Hepatitis B, Chronic | - |
dc.subject.keyword | Carcinoma, Hepatocellular | - |
dc.subject.keyword | MicroRNAs | - |
dc.contributor.affiliatedAuthor | 김, 순선 | - |
dc.contributor.affiliatedAuthor | 조, 효정 | - |
dc.contributor.affiliatedAuthor | 김, 현지 | - |
dc.contributor.affiliatedAuthor | 원, 제환 | - |
dc.contributor.affiliatedAuthor | 김, 진우 | - |
dc.contributor.affiliatedAuthor | 김, 재근 | - |
dc.contributor.affiliatedAuthor | 이, 제희 | - |
dc.contributor.affiliatedAuthor | 김, 보현 | - |
dc.contributor.affiliatedAuthor | 조, 성원 | - |
dc.contributor.affiliatedAuthor | 정, 재연 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.3346/jkms.2018.33.e6 | - |
dc.citation.title | Journal of Korean medical science | - |
dc.citation.volume | 33 | - |
dc.citation.number | 1 | - |
dc.citation.date | 2018 | - |
dc.citation.startPage | e6 | - |
dc.citation.endPage | e6 | - |
dc.identifier.bibliographicCitation | Journal of Korean medical science, 33(1). : e6-e6, 2018 | - |
dc.identifier.eissn | 1598-6357 | - |
dc.relation.journalid | J010118934 | - |
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