Navigating the labyrinth of long non-coding RNAs in colorectal cancer: From chemoresistance to autophagy

Jia-Mei Yu1, Chong-Qi Sun1, Huan-Huan Xu2

  • 1Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.

Insights

Long non-coding RNAs (lncRNAs) regulate autophagy and chemoresistance in colorectal cancer (CRC). Targeting lncRNAs offers a promising strategy to overcome drug resistance in CRC treatment.

Area of Science:

  • Molecular Biology
  • Oncology
  • Genetics

Background:

  • Long non-coding RNAs (lncRNAs) are key regulators in various biological processes, including cancer development.
  • lncRNA expression significantly influences autophagy, a cellular process with a dual role in cancer initiation and progression.
  • Aberrant lncRNA expression is linked to the development of chemoresistance in colorectal cancer (CRC).

Discussion:

  • lncRNAs modulate autophagy, presenting a potential therapeutic target for overcoming chemoresistance in CRC.
  • Recent studies highlight specific lncRNAs (TCONS_00014506 and PRNT) involved in CRC cell autophagy and oxaliplatin resistance.
  • Intervening with lncRNAs that regulate autophagy is emerging as a novel strategy to enhance chemotherapeutic sensitivity in CRC.

Key Insights:

  • lncRNAs play a critical role in regulating autophagy in colorectal cancer.
  • Specific lncRNAs are associated with chemoresistance, particularly to oxaliplatin, in CRC.
  • Modulating lncRNA-mediated autophagy can potentially reverse or overcome chemoresistance in CRC.

Outlook:

  • Further research into lncRNA-autophagy interactions could uncover new therapeutic targets for CRC.
  • Developing lncRNA-based strategies to modulate autophagy may improve treatment outcomes for chemoresistant CRC.
  • This approach holds promise for personalized medicine in colorectal cancer treatment by targeting specific lncRNA pathways.

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