The roles and mechanisms of circular RNAs related to mTOR in cancers

Chunli Cao1,2, Yao Wang1,3, Xinxin Wu1,3

  • 1Department of Biochemistry and Molecular Biology and Zhejiang Key Laboratory of Pathophysiology, Medical School of Ningbo University, Ningbo, China.

Abstract

Insights

Circular RNAs (circRNAs) and mechanistic target of rapamycin (mTOR) play crucial roles in cancer. This review details how circRNA-mTOR interactions regulate various cancers through key signaling pathways, offering potential diagnostic and therapeutic insights.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • Circular RNAs (circRNAs) are covalently closed molecules critical in cancer occurrence, progression, and treatment.
  • Mechanistic target of rapamycin (mTOR) is a central regulator in cancer, influencing proliferation, migration, invasion, autophagy, and apoptosis.

Purpose of the Study:

  • To review the expression, function, and mechanisms of circRNA-associated mTOR in various cancers.
  • To elucidate the role of circRNA-mTOR interactions in cancer signaling pathways and therapeutic strategies.

Main Methods:

  • Comprehensive literature search of PubMed and CNKI databases.
  • Inclusion of articles using keywords: "circRNA," "mTOR," "cancer," "signaling pathway," "biomarker," "diagnosis," "treatment."
  • Analysis of both Chinese and English language publications.

Main Results:

  • CircRNA-associated mTOR regulates cancer progression and therapy across multiple signaling pathways (e.g., PI3K/Akt/mTOR, MAPK/mTOR, AMPK/mTOR).
  • Specific circRNAs are implicated in various cancers, including esophageal, gastric, colorectal, liver, pancreatic, renal, bladder, prostate, ovarian, endometrial, lung, thyroid, glioma, osteosarcoma, leukemia, and breast cancers.
  • CircRNA-mTOR interactions present potential as biomarkers for cancer diagnosis and therapeutic targets.

Conclusions:

  • CircRNA-mTOR signaling is a significant factor in the development and progression of diverse cancers.
  • Understanding these interactions can lead to novel diagnostic tools and targeted cancer therapies.
  • Further research into specific circRNA-mTOR pathways may unlock new treatment avenues.

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