4.3 Article

The prognostic relevance of primary tumor location in patients undergoing resection for pancreatic ductal adenocarcinoma

Journal

ONCOTARGET
Volume 8, Issue 9, Pages 15159-15167

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.14768

Keywords

anatomy; microRNA; pancreatic cancer; recurrence

Funding

  1. National Natural Science Foundation of China [81470892]
  2. Science and Technology Department of Zhejiang Province Program [2014C37061]
  3. Pancreatic Cancer Consortium Kiel [DFG TR 1063/2-1, EG 318/2-1, KA 1346/2-1]

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Different clinical presentations and prognoses have been implied between pancreatic head and body/tail cancers. We aimed to identify the prognostic relevance of primary tumor location in patients undergoing resection for pancreatic ductal adenocarcinoma (PDAC). Thirty-two pairs of patients with strictly matched early stage (II) pancreatic head and body/tail cancers were enrolled. The molecular feature of the two subtypes of PDAC was assessed on the level of miRNA expression. Out of the 64 patients, 34 (53.1%) had tumor recurrence after radical resection during the follow-up period (2.3 +/- 0.8 years). Both overall and tumor-free survival were significantly higher in the patients with pancreatic body/tail cancer compared with those with pancreatic head cancer. Patient age and tumor location were the independent prognostic factors for tumor recurrence. A remarkably lower expression of miR-501-3p and higher expression of miR-375 were found and were further verified in pancreatic body/tail cancer tissues compared with pancreatic head cancer tissues. The low expression of miR-501-3p was significantly associated with a low risk of tumor recurrence. Both, subcutaneous and orthotopic PDAC mouse models presented highly invasive tumor phenotypes upon up-regulated miR-501-3p expression. An in vitro study showed that miR-501-3p promoted the invasiveness of PDAC cells possibly via suppressing E-cadherin. In summary, at resectable early stage, pancreatic body/tail cancer presents a less malignant phenotype associated with deregulation of miR-501-3p compared with pancreatic head cancer.

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