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The effect of Gö6976 on chronic myeloid leukemia in vitro and in vivo.
Cao, Zhen-Rui; Chen, Xiao-Peng; Feng, Min; Hou, Yun-Long; Li, Yan; Hu, Xiao-Lei; Huang, Zheng-Lan; Hu, Jing.
Afiliação
  • Cao ZR; The First Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing, People's Republic of China.
  • Chen XP; The First Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing, People's Republic of China.
  • Feng M; Neuroscience Research Center, Chongqing Medical University, Chongqing, People's Republic of China.
  • Hou YL; Zhoukou Union Osteological Hospital, Zhoukou, People's Republic of China.
  • Li Y; The First Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing, People's Republic of China.
  • Hu XL; Key Laboratory of Laboratory Medical Diagnostics Designated by the Ministry of Education, School of Laboratory Medicine, Chongqing Medical University, Chongqing, People's Republic of China.
  • Huang ZL; Key Laboratory of Laboratory Medical Diagnostics Designated by the Ministry of Education, School of Laboratory Medicine, Chongqing Medical University, Chongqing, People's Republic of China.
  • Hu J; Key Laboratory of Laboratory Medical Diagnostics Designated by the Ministry of Education, School of Laboratory Medicine, Chongqing Medical University, Chongqing, People's Republic of China.
Hematology ; 26(1): 543-551, 2021 Dec.
Article em En | MEDLINE | ID: mdl-34348586
ABSTRACT

Objectives:

Chronic myeloid leukemia (CML) is a malignant tumor of the blood system. Gö6976, as a type of indolocarbazole and shows strong antitumor effects, but there have been no reports on the effect of Gö6976 on CML. The objectives of this research were (1) to explore the impact of Gö6976 on CML in vitro and in vivo; and (2) to explore the drug toxicity of Gö6976 to normal cells and animals.

Methods:

K562 cells and CML mice were used to explore the effect of Gö6976 on CML. Peripheral blood mononuclear cells (PBMCs), CD34+ cells, and healthy mice were used to explore the drug toxicity of Gö6976.

Results:

Cell experiments showed that Gö6976 could inhibit the proliferation of K562 cells and enhance the inhibitory effects of imatinib at 5 µM and 10 µM, but it had little effect on CD34+ cells or PBMCs at concentrations less than 5 µM. Animal experiments showed that 2.5 mg/kg Gö6976 could effectively inhibit the development of CML in mice, and it had almost no effects on healthy mice at 2.5 mg/kg and 10 mg/kg.

Discussion:

Because of the direct inhibitory effect of Gö6976 on CML and its pharmacological enhancement effect on imatinib, it is foreseeable that Gö6976 could become a new type of anti-CML medicine. And the further research is needed.

Conclusion:

Our findings verified that Gö6976 could effectively inhibit CML in vitro and in vivo, and it is almost nontoxic to hematopoietic cells, immune cells, and healthy mice.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carbazóis / Leucemia Mielogênica Crônica BCR-ABL Positiva / Proliferação de Células / Mesilato de Imatinib Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carbazóis / Leucemia Mielogênica Crônica BCR-ABL Positiva / Proliferação de Células / Mesilato de Imatinib Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article