Treatment of Triple Negative Breast Cancer Using RNA-based Nanotherapeutics

Authors

  • Poojan Patel University of Ottawa, Ottawa, ON, Canada
  • Karan Mediratta University of Ottawa, Ottawa, ON, Canada
  • Lisheng Wang University of Ottawa, Ottawa, ON, Canada

DOI:

https://doi.org/10.18192/osurj.v5i2.8056

Abstract

Triple-negative breast cancer (TNBC) is an aggressive and therapeutically challenging subtype
of breast cancer, accounting for a disproportionate number of breast cancer–related deaths. The
absence of ER, PR) and HER2 receptors limits targeted treatment options, leaving chemotherapy
as the primary therapeutic strategy. However, chemotherapy is often associated with significant
toxicity, rapid development of drug resistance, and tumour recurrence due to the enrichment of
cancer stem cells (CSCs). These CSCs exist in interconvertible mesenchymal-like and epithelial
like states, which lead to the excessive growth of one type of CSC and disease relapse when
targeting the other.

This study aimed to develop and evaluate RNA-based nanotherapeutics targeting regulatory
molecules involved in TNBC survival and CSC maintenance. Specifically, the roles of a specific
miRNA and cancer-suppressive mRNA were investigated for their potential to suppress
oncogenic signaling and reduce CSC populations. RNA-loaded nanoparticles were prepared and
characterized to enable efficient delivery into TNBC cells.

The efficacy of these RNA-nanoparticles was assessed through multiple in vitro approaches.
Gene expression changes were quantified using RT-qPCR, while protein-level and CSC
associated markers, including CD44 and ALDH, were analyzed using flow cytometry. Bulk
tumor cell viability was assessed by MTT and PrestoBlue.

It is expected that RNA-nanotherapeutics will reduce both bulk TNBC cell viability and CSC
associated phenotypes, thereby limiting tumour progression and recurrence. This work aims to
contribute to the development of targeted therapies for TNBC by addressing “undruggable
targets through RNA-based approaches to reduce CSC-driven resistance.

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Published

2026-06-17

Issue

Section

Undergraduate Science Research Opportunity Abstracts