Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
J Pediatr Surg ; 52(4): 618-624, 2017 Apr.
Article in English | MEDLINE | ID: mdl-28277300

ABSTRACT

PURPOSE: The aim of this study is to identify the diagnostic values of serum exosomal miRNA-34s of patients with HB in a large Asian group and explore the prognostic value of the exosomal miRNA-34s panel compared with other risk factors. METHODS: We retrospectively reviewed 89 children with HB. Among these patients, 63 patients were included as training group to build the diagnostic model for HB. 26 patients were defined as the validation group. The expressions of miRNA-34s were detected by real-time PCR. The comparison of diagnostic and prognostic performance of serum exosomal miRNA-34s was measured using the area under ROC curve (AUC). RESULTS: For patients in the training group, expression of miRNA-34a, miRNA-34b and miRNA-34c was significantly lower in patients with HB compared with control group in serum exosomes. Between HB training group and the control group, exosomal miRNA-34a, miRNA-34b and miRNA-34c had no significant differences compared with the AFP level in diagnosing HB. The performance of the exosomal miRNA-34s panel in differentiating the HB training group from the control group was superior to the AFP level. The value of the exosomal miRNA-34s panel in predicting prognosis of patients with HB was superior to other risk factors in both training group and validation group. CONCLUSIONS: In this study, we found that the expression of exosomal miRNA-34a, miRNA-34b and miRNA-34c was significantly lower in patients with HB compared with the control group, and we confirmed the exosomal miRNA-34s panel could be defined as a diagnostic and prognostic biomarker for patients with HB. LEVEL OF EVIDENCE: Level II. TYPE OF STUDY: Retrospective Study.


Subject(s)
Biomarkers, Tumor/blood , Exosomes , Hepatoblastoma/diagnosis , Liver Neoplasms/diagnosis , MicroRNAs/blood , Case-Control Studies , Child , Child, Preschool , Female , Follow-Up Studies , Hepatoblastoma/blood , Hepatoblastoma/genetics , Humans , Infant , Infant, Newborn , Liver Neoplasms/blood , Liver Neoplasms/genetics , Male , Prognosis , Real-Time Polymerase Chain Reaction , Retrospective Studies , Risk Factors
2.
J Pediatr Surg ; 51(8): 1355-61, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27046304

ABSTRACT

PURPOSE: The aim of this study is to identify the association between miR-34's family and the prognosis of HB in a large Asian cohort and to explore the interaction of miR-34 with other independent risk factors in the process of affecting prognosis of HB. METHODS: We retrospectively reviewed 78 children with HB (36 female, 42 male) managed in our institutions between 2007 and 2014. The expression of miR-34 was detected by real-time PCR. Prognostic factors were evaluated using Kaplan-Meier curves and Cox proportional hazards models. RESULTS: For the entire cohort of 76 patients, The normalized real-time PCR results showed that all three miRNAs were deregulated in tumor tissues as compared with corresponding noncancerous tissue samples. Descriptive survival statistics and Kaplan-Meier curves suggested that AFP levels, metastases, vascular invasion, PRETEXT stage and miR-34 had prognostic significance in this relatively selected cohort. After that we made miR-34 into different combinations. The results demonstrated that combined low miR-34a and miR-34b (HR:2.212, P=0.016), combined low miR-34a and miR-34c (HR:1.984, P=0.025) and combined low miR-34a, miR-34b and miR-34c (HR:3.569, P=0.001) were independent prognostic factors of HB. We further conduct stratified analysis of the impact of other identified risk factors on the combined low of three miR-34. CONCLUSIONS: In this study, we found that miR-34s were deregulated in tumor tissues compared with corresponding noncancerous tissue samples. We also confirmed that combined low miR-34 is an independent prognostic factor related with HB.


Subject(s)
Biomarkers, Tumor/metabolism , Hepatoblastoma/metabolism , Liver Neoplasms/metabolism , MicroRNAs/metabolism , China/epidemiology , Female , Hepatoblastoma/mortality , Humans , Infant , Liver Neoplasms/mortality , Male , Prognosis , Real-Time Polymerase Chain Reaction , Retrospective Studies , Risk Factors , Survival Analysis , Time Factors , alpha-Fetoproteins/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...