Targeting ncRNA control networks with engineered exosomes to overcome therapy resistance in thyroid cancer.

Crit Rev Oncol HematolJun 20, 2026 (epub)

Anjani H Turaga, Brenden M Finnerty, Rasa Zarnegar et al.

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In 30 seconds

This systematic review evaluated the role of exosomal non-coding RNAs (ncRNAs) in therapy resistance in radioactive iodine-refractory papillary thyroid cancer (RAIR-PTC). The review included 96 high-quality studies and found that ncRNA regulatory networks suppress sodium-iodide symporter (NIS) expression, contributing to a 10-year survival rate below 10%. Exosomes may serve as effective delivery vehicles for therapeutic ncRNAs.

Key findings

  • RAIR-PTC is characterized by impaired NIS expression and activation of oncogenic pathways.
  • 96 high-quality studies were included after screening 961 publications.
  • Convergent ncRNA networks sustain dedifferentiation and impaired iodide transport.
  • Engineered exosomes can transport therapeutic ncRNA payloads to restore iodine-handling pathways.

Why it matters

Understanding the role of ncRNAs in therapy resistance can inform the development of targeted therapies for RAIR-PTC, potentially improving patient outcomes in a challenging clinical scenario.

Source

Published in Crit Rev Oncol Hematol. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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