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PI3K/AKT/mTOR Targeting in Colorectal Cancer Radiotherapy: A Systematic Review.
S N Mousavikia1,2, L Darvish3,4, A A Firouzjaei5
1Medical Physics Research Center, Basic Sciences Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran.
Targeting the PI3K/AKT/mTOR pathway can overcome radioresistance in colorectal cancer (CRC). Combining pathway inhibitors with radiotherapy enhances treatment efficacy and improves patient outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Radioresistance significantly limits radiotherapy effectiveness in colorectal cancer (CRC) treatment.
- The PI3K/AKT/mTOR signaling pathway is implicated in CRC progression and the development of radioresistance.
- Targeting the PI3K/AKT/mTOR pathway presents a potential strategy to enhance oncotherapy outcomes.
Purpose of the Study:
- To systematically review the effects of PI3K/AKT/mTOR pathway inhibitors on improving radiotherapy efficacy in colorectal cancer.
- To evaluate the potential of combination therapies involving PI3K/AKT/mTOR inhibitors and radiotherapy for CRC treatment.
Main Methods:
- Systematic literature search across major scientific databases (Scopus, PubMed, Web of Science, Embase, Medline).
- Inclusion of studies investigating PI3K/AKT/mTOR pathway inhibitors in combination with radiotherapy for colorectal cancer.
- Analysis of preclinical and clinical trial data.
Main Results:
- Review of 32 articles (27 preclinical, 5 clinical trials) on PI3K/AKT/mTOR inhibitors and radiotherapy.
- Combination therapy demonstrated reduced tumor survival, induced apoptosis, and cell cycle arrest, enhancing radiosensitivity.
- Favorable treatment outcomes observed in colorectal cancer patients receiving combination therapy, despite limited studies.
Conclusions:
- The PI3K/AKT/mTOR pathway is crucial for colorectal cancer cell survival.
- Inhibiting this pathway can potentiate radiotherapy efficacy.
- Findings support further research and clinical application of PI3K/AKT/mTOR inhibitors in CRC treatment.
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