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Micro-RNA Expression Patterns Predict Metastatic Spread in Solid Pseudopapillary Neoplasms of the Pancreas
Shmuel Jaffe Cohen1, Michail Papoulas2, Nadine Graubardt1
1Surgical Division Research Laboratory, Tel-Aviv Sourasky Medical Center Affiliated to the Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Frontiers in Oncology
|April 2, 2020
Summary
Solid pseudopapillary neoplasm (SPN) is a rare pancreatic cancer. Tumor size predicts metastasis, while specific microRNAs may indicate malignant behavior, aiding in prognosis prediction for SPN patients.
Area of Science:
- Oncology
- Genomics
- Pancreatic Cancer Research
Background:
- Solid pseudopapillary neoplasm (SPN) of the pancreas is rare with low metastatic potential.
- Predicting malignant behavior in SPN is challenging due to rarity and excellent prognosis.
- Identifying prognostic factors for SPN metastasis is crucial for patient management.
Purpose of the Study:
- To identify clinical, histological, and microRNA patterns associated with metastatic SPN.
- To determine reliable prognostic factors for predicting SPN malignant behavior.
- To explore microRNA expression differences between localized and metastatic SPN.
Main Methods:
- Retrospective analysis of 35 patients operated for SPN (1995-2018).
- Collection of clinical and pathological data, including tumor size and KI67.
- MicroRNA expression profiling of 2,578 microRNAs in normal, localized, and metastatic tissues using microarray and RT-PCR.
Main Results:
- Tumor size was the only clinical factor associated with metastasis (p < 0.012).
- Histological features and KI67 were not predictive of metastasis.
- Differential expression of six microRNAs (miR-184, miR-10a, miR-887, miR-375, miR-217, miR-200c) identified between metastatic and localized SPN.
Conclusions:
- Tumor size is a significant clinical predictor of metastasis in SPN.
- Histological features are unreliable for predicting SPN metastasis.
- A panel of six microRNAs shows potential for predicting SPN tumor behavior, requiring further validation.
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