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Berberine and cinnamaldehyde together prevent lung carcinogenesis
Mingjing Meng1, Shengnan Geng1, Zhenhua Du1
1Institute of Pharmacy, Pharmacy College of Henan University, Jinming District, Kaifeng, Henan Province 475004, China.
Oncotarget
|November 5, 2017
Summary
Berberine and cinnamaldehyde synergistically starve lung cancer cells by activating AMP-activated protein kinase (AMPK) and downregulating aquaporin-1 (AQP-1), inhibiting tumor growth.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Nutrient restriction is a promising cancer therapy.
- Berberine and cinnamaldehyde activate AMP-activated protein kinase (AMPK).
Purpose of the Study:
- To investigate if berberine and cinnamaldehyde synergistically prevent lung carcinogenesis via tumor cell starvation.
- To explore the underlying molecular mechanisms involving AMPK, mTOR, AQP-1, and NF-κB.
Main Methods:
- Urethane-induced lung carcinogenesis model in mice.
- In vitro studies using A549 lung cancer cells.
- Analysis of AMPK, mTOR, AQP-1, and NF-κB expression.
- Assessment of cell apoptosis, proliferation, autophagy, and wound healing.
- Inhibition studies using rapamycin, HgCl2, and Z-VAD-FMK.
Main Results:
- Combined berberine and cinnamaldehyde reduced lung carcinogenesis in mice and reversed aberrant protein expression.
- In vitro, the combination induced apoptosis, inhibited proliferation, autophagy, and wound healing.
- Upregulation of AMPK and downregulation of AQP-1 were observed.
- Effects were mediated by mTOR and AQP-1, but not caspase pathways.
- Reduced substance permeability and intracellular ATP concentrations were noted.
Conclusions:
- Berberine and cinnamaldehyde combination effectively starves lung tumor cells.
- The mechanism involves AMPK-mediated downregulation of AQP-1, limiting nutrient uptake.
- This strategy shows potential for lung cancer prevention and treatment.
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