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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.
Background:
Circular RNAs (circRNAs) are stable molecules with covalently closed structures that have an irreplaceable role in the occurrence, progression, and even treatment of plenty of cancers. Mammalian/mechanistic target of rapamycin (mTOR) is a key regulator in cancers and plays several biological functions, such as proliferation, migration, invasion, autophagy, and apoptosis.
Methods:
All data were collected through PubMed and CNKI, using terms including "circRNA," "mTOR," "caner," "signaling pathway," "biomarker," "diagnosis," "treatment." Articles published in Chinese and English were included.
Results:
In this review, the expression, function, and mechanism of circRNA-associated mTOR in cancers were described. CircRNA-associated-mTOR can regulate the progression and therapy of a variety of cancers in multiple signaling pathways, such as phosphatidylinositol-3-kinase (PI3K)/protein kinase B (Akt)/mTOR, mitogen-activated protein kinase (MAPK)/mTOR, and AMP-activated protein kinase (AMPK)/mTOR axis. These cancers including esophageal carcinoma (circLPAR3, ciRS-7), gastric cancer (circNRIP1, hsa_circ_0010882, hsa_circ_0000117, hsa_circ_0072309, and circST3GAL6), colorectal cancer (hsa_circ_0000392, hsa_circ_0084927, hsa_circ_0104631, and circFBXW7), liver cancer (circC16orf62, hsa_circ_100338, hsa_circ_0004001, hsa_circ_0004123, hsa_circ_0075792, hsa_circ_0079299, and hsa_circ_0002130), pancreatic cancer (circ-IARS and circRHOBTB3), renal carcinoma (ciRS-7), bladder cancer (circUBE2K), prostate cancer (circMBOAT2 and circ-ITCH), ovarian cancer (circEEF2, circRAB11FIP1, circMYLK, and circTPCN), endometrial cancer (hsa_circ_0002577 and circWHSC1), lung cancer (circHIPK3, hsa_circ_0001666), thyroid cancer (hsa_circ_0007694 and hsa_circ_0008274), glioma (circGFRA1, circ-MAPK4, circPCMTD1, and hsa_circ_0037251), osteosarcoma (circTCF25), leukemia (circ-PRKDC), and breast cancer (hsa_circ_0000199, circUBAP2, and circWHSC1).
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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