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Updated: Jun 4, 2026

In Vitro and In Vivo Models to Study Corneal Endothelial-mesenchymal Transition
Published on: August 20, 2016
[mTOR inhibitor]
1Dept. of Clinical Oncology, Aichi Cancer Center Hospital, Japan.
Abstract:
Mammalian target of rapamycin(mTOR)exists downstream in the PI3K/AKT signal transmission pathway that is constantly activated in many cancers. It regulates translation of mRNA that codes for proteins involved in survival signals, such as for the cell cycle and apoptosis, by phosphorylation of p70S6K and 4E-BP1 that are further downstream. Thus, mTOR promotes cell proliferation and translation. It is also related to the growth and proliferation of cancer vascular endothelial cells. Inhibition of mTOR has been shown to lead to the inhibition of cancer cell proliferation and cancer angiogenesis, which are activated by mTOR, and to have an antitumor effect. In recent years, advances have been made in the development of drugs that target mTOR; that is, mTOR inhibitors. These drugs are being incorporated into the first and second-line therapies as standard treatment for renal cell cancer. The usefulness of mTOR has also been shown in pancreatic neuroendocrine tumor. The next task is to discover a clinically effective biomarker that predicts effect and toxicity of mTOR.
Insights
Mammalian target of rapamycin (mTOR) signaling drives cancer growth and proliferation. Inhibiting mTOR shows promise as an antitumor strategy, particularly in renal cell cancer and pancreatic neuroendocrine tumors.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Mammalian target of rapamycin (mTOR) is a key signaling pathway downstream of PI3K/AKT, frequently activated in various cancers.
- mTOR regulates mRNA translation for proteins involved in cell cycle, apoptosis, and survival, promoting cancer cell proliferation and angiogenesis.
- mTOR also influences the growth and proliferation of cancer vascular endothelial cells.
Purpose of the Study:
- To review the role of mTOR in cancer development and progression.
- To discuss the therapeutic potential of mTOR inhibitors in cancer treatment.
- To highlight the need for biomarkers predicting mTOR inhibitor efficacy and toxicity.
Main Methods:
- Literature review of studies on mTOR signaling in cancer.
- Analysis of clinical trial data for mTOR inhibitors.
- Examination of preclinical research on mTOR targeted therapies.
Main Results:
- mTOR inhibition demonstrates antitumor effects by suppressing cancer cell proliferation and angiogenesis.
- mTOR inhibitors are established as standard treatments for renal cell cancer and show utility in pancreatic neuroendocrine tumors.
- The development of effective biomarkers for predicting mTOR inhibitor response and toxicity is an ongoing challenge.
Conclusions:
- mTOR is a critical mediator of cancer cell growth and angiogenesis, making it a viable therapeutic target.
- mTOR inhibitors represent a significant advancement in cancer therapy, with established roles in specific malignancies.
- Future research should focus on identifying predictive biomarkers to optimize mTOR inhibitor therapy and improve patient outcomes.
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