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Intracellular Phosphoflow Cytometry of Acute Myeloid Leukemia Patient-Derived Xenotransplants
Published on: June 6, 2025
Mogrol represents a novel leukemia therapeutic, via ERK and STAT3 inhibition
Can Liu1, Yan Zeng2, Long-Hai Dai2
1Beijing University of Agriculture Beijing 102206, China ; National Engineering Laboratory for Industrial Enzymes, Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences Tianjin 300308, China ; Key Laboratory of Urban Agriculture (North) of Ministry of Agriculture P. R. China, Beijing University of Agriculture Beijing 102206, China.
Abstract:
Unlike solid tumors, the primary strategy for leukemia treatment is chemotherapy. However, leukemia chemotherapy is associated with adverse drug effects and drug resistance. Therefore, it is imperative to identify novel agents that effectively treat leukemia while minimizing adverse effects. The Raf/MEK/extracellular regulated kinase (ERK) and signal transducer and activator of transcription 3 (STAT3) pathways have been implicated in leukemia carcinogenesis, and provide novel molecular targets for therapeutic intervention in cancer. Mogrol, a biometabolite of mogrosides found in Siraitia grosvenorii, has exhibited anti-cancer activities; however, the underlying mechanism of this effect remains unclear. To clarify its anti-cancer activity and mechanism of action, we treated K562 leukemia cells with mogrol. Mogrol suppressed leukemia cell growth via inhibition of the ERK1/2 and STAT3 pathways, in particular, through the suppression of p-ERK1/2 and p-STAT3. Inhibition of these pathways suppressed Bcl-2 expression, thereby inducing K562 cell apoptosis. Furthermore, mogrol enhanced p21 expression, resulting in G0/G1 cell cycle arrest. The findings provide new perspectives regarding the role of mogrol in leukemia treatment.
Insights
Mogrol, a natural compound, effectively inhibits leukemia cell growth by targeting the ERK1/2 and STAT3 pathways. This novel leukemia treatment induces apoptosis and cell cycle arrest, offering a promising alternative to chemotherapy.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Chemotherapy is the primary leukemia treatment but causes adverse effects and drug resistance.
- Novel therapeutic agents are needed to effectively treat leukemia with fewer side effects.
- The Raf/MEK/ERK and STAT3 pathways are crucial in leukemia development and represent potential therapeutic targets.
Purpose of the Study:
- To investigate the anti-cancer activity of mogrol, a biometabolite of mogrosides.
- To elucidate the mechanism of action of mogrol in K562 leukemia cells.
- To explore mogrol as a potential novel agent for leukemia treatment.
Main Methods:
- K562 leukemia cells were treated with mogrol.
- The effects of mogrol on ERK1/2 and STAT3 pathways were analyzed.
- Expression levels of p-ERK1/2, p-STAT3, Bcl-2, and p21 were assessed.
- Apoptosis and cell cycle arrest were evaluated.
Main Results:
- Mogrol suppressed K562 leukemia cell growth.
- Mogrol inhibited the ERK1/2 and STAT3 pathways by reducing p-ERK1/2 and p-STAT3 levels.
- Mogrol induced apoptosis by suppressing Bcl-2 expression.
- Mogrol promoted G0/G1 cell cycle arrest through enhanced p21 expression.
Conclusions:
- Mogrol exhibits anti-leukemia effects by inhibiting the ERK1/2 and STAT3 signaling pathways.
- Mogrol induces apoptosis and cell cycle arrest in leukemia cells.
- Mogrol represents a promising novel therapeutic candidate for leukemia treatment.
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