Your browser doesn't support javascript.
loading
[Thiotert Induces Myelodysplastic Syndromes Cells Apoptosis by Activating Oxidative Stress].
Jing, Qiang-An; Zhou, Chao-Ting; Wu, Yun-Yi; Ke, Xia; Tong, Xiang-Min.
Afiliación
  • Jing QA; Institute of Clinical Medicine, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou 310006, Zhejiang Province, China.
  • Zhou CT; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou 310014, Zhejiang Province, China.
  • Wu YY; Institute of Clinical Medicine, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou 310006, Zhejiang Province, China.
  • Ke X; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou 310014, Zhejiang Province, China.
  • Tong XM; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou 310014, Zhejiang Province, China.
Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 32(4): 1181-1185, 2024 Aug.
Article en Zh | MEDLINE | ID: mdl-39192416
ABSTRACT

OBJECTIVE:

To explore whether thiotert treatment can inhibit proliferation and induce apoptosis in myelodysplastic syndromes (MDS) cells.

METHODS:

CCK-8 assay was used for determining the cytotoxicity of thiotert to MDS cell line SKM-1 and the reversal effect of GSH, NAC, and Z-VAD-FMK on thiotert-induced inhibition of cell viability. EdU assay was deployed to detect the cell proliferation ability. Intracellular reactive oxygen species (ROS) was measured by flow cytometry after DCFH-DA staining. The expression of DNA damage- and apoptosis-related proteins was detected by Western blot.

RESULTS:

Thiotert treatment significantly suppressed the cell viability and proliferation ability in SKM-1 cells. A large amount of ROS generation and markedly elevated C-PARP, C-Caspase 3, and γ-H2AX were observed after thiotert administration, while BCL-2 was significantly decreased. In addition, GSH, NAC, and Z-VAD-FMK were able to mitigate the cytotoxicity of thiotert on SKM-1 cells.

CONCLUSION:

Thiotert can promote MDS cell apoptosis by mediating ROS production and pro-apoptotic proteins expression.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Especies Reactivas de Oxígeno / Apoptosis / Estrés Oxidativo / Proliferación Celular Límite: Humans Idioma: Zh Revista: Zhongguo Shi Yan Xue Ye Xue Za Zhi Asunto de la revista: HEMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Especies Reactivas de Oxígeno / Apoptosis / Estrés Oxidativo / Proliferación Celular Límite: Humans Idioma: Zh Revista: Zhongguo Shi Yan Xue Ye Xue Za Zhi Asunto de la revista: HEMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: China