Protein Arginine Methylation Patterns in Plasma Small Extracellular Vesicles Are Altered in Patients with Early-Stage Pancreatic Ductal Adenocarcinoma

Author:

Bhandari Kritisha1ORCID,Kong Jeng Shi1,Morris Katherine2ORCID,Xu Chao3ORCID,Ding Wei-Qun1ORCID

Affiliation:

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

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

3. Department of Biostatistics & Epidemiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA

Abstract

Small extracellular vesicles (sEVs) contain lipids, proteins and nucleic acids, which often resemble their cells of origin. Therefore, plasma sEVs are considered valuable resources for cancer biomarker development. However, previous efforts have been largely focused on the level of proteins and miRNAs in plasma sEVs, and the post-translational modifications of sEV proteins, such as arginine methylation, have not been explored. Protein arginine methylation, a relatively stable post-translational modification, is a newly described molecular feature of PDAC. The present study examined arginine methylation patterns in plasma sEVs derived from patients with early-stage PDAC (n = 23) and matched controls. By utilizing the arginine methylation-specific antibodies for western blotting, we found that protein arginine methylation patterns in plasma sEVs are altered in patients with early-stage PDAC. Specifically, we observed a reduction in the level of symmetric dimethyl arginine (SDMA) in plasma sEV proteins derived from patients with early- and late-stage PDAC. Importantly, immunoprecipitation followed by proteomics analysis identified a number of arginine-methylated proteins exclusively present in plasma sEVs derived from patients with early-stage PDAC. These results indicate that arginine methylation patterns in plasma sEVs are potential indicators of PDAC, a new concept meriting further investigation.

Funder

Congressionally Directed Medical Research Programs

National Institute of General Medical Sciences

Presbyterian Health Foundation and the National Cancer Institute Cancer Center

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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