[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.

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.

Related Concept Videos

PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
5.1K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
3.6K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

1.5K
Interactions Between Signaling Pathways01:19

Interactions Between Signaling Pathways

Signaling cascades usually lack linearity. Multiple pathways interact and regulate one another, allowing cells to integrate and respond to diverse environmental stimuli.
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
4.6K
The JAK-STAT Signaling Pathway01:20

The JAK-STAT Signaling Pathway

Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as  SH2...
10.1K
Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl...
2.9K