Oncotarget

Research Papers:

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

Yi-Fan Xu, Bethany N. Hannafon, Yan D. Zhao, Russell G. Postier and Wei-Qun Ding _

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Oncotarget. 2017; 8:77028-77040. https://doi.org/10.18632/oncotarget.20332

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Abstract

Yi-Fan Xu1, Bethany N. Hannafon1, Yan D. Zhao2, Russell G. Postier3 and Wei-Qun Ding1

1Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, OK 73104, USA

2Department of Biostatistics and Epidemiology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, OK 73104, USA

3Department of Surgery, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, OK 73104, USA

Correspondence to:

Wei-Qun Ding, email: [email protected]

Keywords: exosome, microRNAs, pancreatic cancer, plasma biomarkers, early detection

Received: April 27, 2017     Accepted: July 28, 2017     Published: August 18, 2017

ABSTRACT

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 miR-1246, are highly enriched in pancreatic cancer exosomes and elevated in plasma exosomes of patients with localized pancreatic cancer.


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