Characterization and Application of Highly Specific 2’-F RNA Aptamers Targeting a Potentially Novel Pancreatic Ductal Adenocarcinoma (PDAC) Biomarker(s) Public Deposited

Downloadable Content

Download PDF
Last Modified
  • March 19, 2019
Creator
  • Claypool, Sarah
    • Affiliation: Eshelman School of Pharmacy, Division of Chemical Biology and Medicinal Chemistry
Abstract
  • Pancreatic ductal adenocarcinoma (PDAC) has an extremely dismal 5-year survival rate of only 6%. Highly specific targeting ligands that can aid in early stage diagnosis and improved treatment are urgently needed. To address the challenge, cell-SELEX was used to develop a panel of partially modified, 2’-F RNA aptamers that highly selectively recognize pancreatic ductal adenocarcinoma cells. One of the best aptamers, termed 1502, was optimized to be the shortest target-binding motif that retains the target-binding specificity and affinity, and further chemically synthesized with various 3’ and 5’ functional groups for characterization and application. Using hyperthermia treatment mediated by gold nanoparticles targeted with this optimized aptamer, it was found that the aptamer recognizes all the eleven pancreatic cancer cell lines we have tested, but not normal pancreas, nor numerous non-pancreatic cancer cells. Additionally, a hybrid lipid-PLGA nanoparticle was developed that can carry small molecule organic dyes or drugs for a therapeutic delivery application. With a 5’-modified variation of aptamer 1502, this nanoparticle was functionalized to target PDAC cells, and subsequently internalized to deliver a cytotoxic drug, resulting in selective cell-killing. We believe that this aptamer can be translated to in vivo delivery models and can be used to identify a putative novel biomarker of pancreatic ductal adenocarcinoma.
Date of publication
Keyword
Subject
Identifier
Resource type
Rights statement
  • In Copyright
Advisor
  • Li, Zibo
  • Lai, Samuel
  • Jarstfer, Michael
  • Wiltshire, Timothy
  • Liu, Rihe
  • Tropsha, Alexander
Degree
  • Doctor of Philosophy
Degree granting institution
  • University of North Carolina at Chapel Hill Graduate School
Graduation year
  • 2015
Language
Publisher
Place of publication
  • Chapel Hill, NC
Access
  • There are no restrictions to this item.
Parents:

This work has no parents.

Items