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Submission Status
Withdrawn
Abstract
Abstract Title
Circulating microRNA profiling for prediction of oncological outcomes in prostate cancer patients following radical prostatectomy
Presentation Type
Podium Abstract
Manuscript Type
Basic Research
Abstract Category *
Oncology: Prostate
Author's Information
Number of Authors (including submitting/presenting author) *
3
No more than 10 authors can be listed (as per the Good Publication Practice (GPP) Guidelines).
Please ensure the authors are listed in the right order.
Country
Japan
Co-author 1
Fumihiko Urabe furabe0809@gmail.com The Jikei University School of Medicine Urology Tokyo Japan *
Co-author 2
Kagenori Ito ito.kagenori@gmail.com The Jikei University School of Medicine Urology Tokyo Japan -
Co-author 3
Takahiro Kimura tkimura0809@gmail.com The Jikei Univeristy School of Medicine Urology Tokyo Japan -
Co-author 4
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Co-author 5
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Co-author 6
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Co-author 7
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Co-author 8
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Co-author 9
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Co-author 10
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Co-author 11
Co-author 12
Co-author 13
Co-author 14
Co-author 15
Co-author 16
Co-author 17
Co-author 18
Co-author 19
Co-author 20
Abstract Content
Introduction
Although radical prostatectomy is associated with good long-term oncological outcomes, approximately 30% of patients present biochemical recurrence, whereupon salvage treatments are required. Identification of novel molecular biomarkers to predict cancer behavior is clinically important. Here, we developed a novel miRNA-based prognostic model for patients who underwent radical prostatectomy.
Materials and Methods
Total RNA was extracted from 300 μL of serum using the 3DGene RNA Extraction Reagent (Toray Industries, Inc.). The comprehensive miRNA profiles of patients with bladder cancer were analyzed using the 3D-Gene miRNA Labelling kit and the 3D-Gene Human miRNA. We retrospectively investigated the clinical records of 295 patients who underwent radical prostatectomy between 2009 and 2017. We randomly assigned these cases into training or validation sets. The prognostic model was constructed using Fisher linear discriminant analysis in the training set, and we evaluated its performance in the validation set. To normalize the signals among the microarrays tested, three preselected internal control miRNAs (miR-149-3p, miR-2861, and miR-4463) were used.
Results
Overall, 72 patients had biochemical recurrence. A prediction model was constructed using a combination of three miRNAs (miR-3147, miR-4513, and miR-4728-5p) and two pathological factors (pathological T stage and Gleason score). In the validation set, the predictive performance of the model was confirmed to be accurate (AUC, 0.80; sensitivity, 0.78; specificity, 0.76) (Figure 1a). Additionally, Kaplan–Meier analysis revealed that the patients with a low prediction index had significantly longer recurrence-free survival than those with a high index (P<0.001) (Figure 1b).
Conclusions
We established a prognostic model using serum miRNAs that can be used to stratify postoperative patients with PCa as having a high risk or a low risk of BCR. This model may be helpful for physicians in determining a follow-up strategy for patients after RP.
Keywords
microRNA, liquid biopsy
Figure 1
https://storage.unitedwebnetwork.com/files/1237/44ed80aadec22a6daac8508c78db0426.jpg
Figure 1 Caption
Figure 1 (a) ROC curve analysis of the prediction index in the validation set. (b) Kaplan–Meier analysis of biochemical recurrence-free survival in the validation set.
Figure 2
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Character Count
1723
Vimeo Link
Presentation Details
Session
Free Paper Podium(14): Oncology Prostate (D)
Date
Aug. 16 (Sat.)
Time
14:36 - 14:42
Presentation Order
12