4.3 Article

Plasma exosome miR-196a and miR-1246 are potential indicators of localized pancreatic cancer

Journal

ONCOTARGET
Volume 8, Issue 44, Pages 77028-77040

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.20332

Keywords

exosome; microRNAs; pancreatic cancer; plasma biomarkers; early detection

Funding

  1. National Institute of General Medical Sciences of the National Institutes of Health [U54GM104938]
  2. Oklahoma Center for the Advancement of Science and Technology [HR14-147]
  3. Presbyterian Health Foundation
  4. Peggy and Charles Stephenson Cancer Center
  5. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [U54GM104938] Funding Source: NIH RePORTER

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Patients with localized pancreatic cancer (stage I and stage IIA) have a much higher survival rate than those presenting at later stages, yet early detection remains a challenge to this malignancy. The aim of this study was to evaluate whether exosome miRNA signatures are indicative of localized pancreatic cancer. Exosomes were collected from the conditioned media of pancreatic cancer cell lines and plasma samples of localized pancreatic cancer patients (Stage I-IIA, n= 15), and healthy subjects (n= 15). Cellular and exosome miRNAs from pancreatic cancer cell lines were profiled by next-generation small RNA sequencing. Plasma exosome miRNA expression was analyzed by qRT-PCR. We found that certain miRNAs, such as miR-196a and miR-1246, are highly enriched in pancreatic cancer exosomes. Consistently, plasma exosome miR-196a and miR-1246 levels were significantly elevated in pancreatic cancer patients as compared to healthy subjects. An analysis of the cancer subtypes indicated that plasma exosome miR-196a is a better indicator of pancreatic ductal adenocarcinoma (PDAC), whereas plasma exosome miR-1246 is significantly elevated in patients with intraductal papillary mucinous neoplasms (IPMN). In contrast, there were no differences in the plasma exosome miR-196a and miR-1246 levels between patients with pancreatic neuroendocrine tumors (NET) and healthy subjects. In conclusion, we demonstrate that certain miRNA species, such as miR-196a and miR1246, are highly enriched in pancreatic cancer exosomes and elevated in plasma exosomes of patients with localized pancreatic cancer.

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