Icaritin Shows Potent Anti-Leukemia Activity on Chronic Myeloid Leukemia In Vitro and In Vivo by Regulating MAPK/ERK/JNK and JAK2/STAT3/AKT Signalings
2011

Icaritin's Anti-Leukemia Effects on Chronic Myeloid Leukemia

Sample size: 24 publication 10 minutes Evidence: moderate

Author Information

Author(s): Zhu Jian feng, Li Zi jian, Zhang Guang sen, Meng Kun, Kuang Wen yong, Li Jin, Zhou Xin fu, Li Rui juan, Peng Hong ling, Dai Chong wen, Shen Jian Kai, Gong Fan jie, Xu Yun xiao, Liu Su fang

Primary Institution: Division of Hematology, Institute of Molecular Hematology, The Second Xiang-Ya Hospital, Central South University, Changsha, Hunan, People's Republic of China

Hypothesis

To explore the effects of Icaritin on chronic myeloid leukemia (CML) cells and underlying mechanisms.

Conclusion

Icaritin from Chinese herb medicine may be a potential anti-CML agent with low adverse effect.

Supporting Evidence

  • Icaritin inhibited proliferation of K562 cells with an IC50 of 8 µM.
  • Icaritin induced apoptosis in CML cells as shown by Annexin V staining.
  • Icaritin promoted erythroid differentiation of K562 cells.
  • Icaritin reduced Jak-2, p-Stat3, and p-Akt expression.
  • Icaritin prolonged the lifespan of NOD-SCID mice inoculated with K562 cells.

Takeaway

Icaritin is a natural compound that can help fight a type of blood cancer called chronic myeloid leukemia by stopping cancer cells from growing and helping them die.

Methodology

CML cells were treated with Icaritin, and cell proliferation and apoptosis were analyzed using MTT assay and Annexin V staining, respectively. In vivo effects were tested in NOD-SCID mice.

Potential Biases

Potential bias due to funding from a company that produces Icaritin.

Limitations

The study primarily focuses on in vitro and in vivo models, and further clinical studies are needed to confirm the findings.

Participant Demographics

24 CML patients (14 CML-CP and 10 CML-BC) and 11 healthy controls.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0023720

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