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[Recent advances in non-coding RNA-mediated PI3K/AKT/mTOR signaling pathway regulation involved in triple-negative
Zhu Huang1,2, Wen-Jing Li1, Zi-Juan Song1
1Innovation Center of Targeted Development of Medicinal Resources, School of Life Sciences and Food Engineering, Anqing Normal University, Anqing 246133, China.
Abstract:
Triple-negative breast cancer (TNBC) is characterized by high invasion and metastasis, poor prognosis, and high mortality, making it the most aggressive form of breast cancer. Currently, there is still a lack of effective therapeutic targets for TNBC. Aberrant activation of phosphatidylinositol 3-kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) pathway is prevalent in TNBC, leading to increased resistance to chemotherapeutic agents and poor prognosis. Non-coding RNA (ncRNA), including microRNA (miRNA), long non-coding RNA (lncRNA) and circular RNA (circRNA), are involved in a variety of biological processes and can be used as oncogenes or tumor suppressor genes to regulate the PI3K/AKT/mTOR pathway to promote or inhibit the occurrence and development of TNBC. This article reviews some important miRNA, lncRNA, circRNA, and their targets and molecular mechanisms that regulate the PI3K/AKT/mTOR pathway in TNBC, hoping to open up new avenues for the research of TNBC and ultimately promote the development of precise and effective treatments for TNBC.
Insights
Triple-negative breast cancer (TNBC) is aggressive, lacking effective treatments. Non-coding RNAs (ncRNAs) like miRNAs, lncRNAs, and circRNAs regulate the PI3K/AKT/mTOR pathway, offering potential therapeutic targets for TNBC.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Triple-negative breast cancer (TNBC) exhibits high metastasis, poor prognosis, and mortality.
- The phosphatidylinositol 3-kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) pathway is frequently activated in TNBC, contributing to therapeutic resistance.
Purpose of the Study:
- To review the roles of non-coding RNAs (ncRNAs) in regulating the PI3K/AKT/mTOR pathway in TNBC.
- To explore potential therapeutic strategies targeting ncRNAs for TNBC treatment.
Main Methods:
- Literature review of studies on ncRNAs, PI3K/AKT/mTOR pathway, and TNBC.
- Analysis of molecular mechanisms involving microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs) in TNBC.
Main Results:
- ncRNAs act as oncogenes or tumor suppressors by modulating the PI3K/AKT/mTOR pathway in TNBC.
- Specific miRNAs, lncRNAs, and circRNAs and their targets involved in TNBC progression were identified.
Conclusions:
- Dysregulation of the PI3K/AKT/mTOR pathway by ncRNAs is crucial in TNBC development.
- Targeting ncRNAs presents a promising avenue for developing precise and effective TNBC therapies.
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