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[Effects of Aptamer-siRNA Nucleic Acid Compound on Growth and Apoptosis in Myeloid Leukemia Cell Line K562].
Ping, Juan; Shen, Zhi-Hui; Wang, Bao-Quan; Zhao, Na; Li, Rui; Li, Mian; Pang, Xiao-Bin; Chen, Chuan-Bo.
  • Ping J; Department of Gastroenterology, The Huaihe Clincal College of Henan University, Kaifeng 475004, Henan Province, China.
  • Shen ZH; Department of Hematology and Oncology, The Tumour Hospital of Zhengzhou University, Zhengzhou 450009, Henan Province, China.
  • Wang BQ; Department of Gastroenterology, The Huaihe Clincal College of Henan University, Kaifeng 475004, Henan Province, China.
  • Zhao N; Department of Hematology and Oncology, The Tumour Hospital of Zhengzhou University, Zhengzhou 450009, Henan Province, China.
  • Li R; Department of Hematology and Oncology, The Xijing Hospital of Fourth Military Medical University, Xi'an 730011, Shanxi Province, China.
  • Li M; Department of Chemibiology, The Pharmaceutical College, Henan University, Kaifeng 475001, Henan Province, China.
  • Pang XB; Department of Chemibiology, The Pharmaceutical College, Henan University, Kaifeng 475001, Henan Province, China.
  • Chen CB; Department of Gastroenterology, The Huaihe Clincal College of Henan University, Kaifeng 475004, Henan Province, China. E-mail: chenchuanbo@henan.edu.cn.
Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 23(2): 381-5, 2015 Apr.
Article en Zh | MEDLINE | ID: mdl-25948189
ABSTRACT

OBJECTIVE:

To explore the effects of aptamer-siRNA nucleic acid compound on growth and apoptosis in myeloid leukemia cell line K562.

METHODS:

the changes of cellular morphology and structure were observed by using fluorescence microscope, laser confocal microscope, JEM-4000EX transmission electron microscopy; MTT assay were performed to evaluate the sensibility of K562 cells to aptamer-siRNA compound, the apoptosis was detected by DNA gel electro-phoresis.

RESULTS:

The remarkably changes of morphology and structure of K562 cells treated with 200 µmol/L aptamer-siRNA were observed under fluorescence microscopy and electromicroscopy. As compared with control, the aptamer-siRNA compound showed more inhibitory effect on K562 cells and there was significant difference (P<0.05). The MTT assay showed that the IC50 value of aptamer-siRNA compound for K562 cells was 150 µmol/L. According to agarose gel electrophoresis observation, when the aptamer-siRNA compound showed effect on K562 cells, the typical DNA lader could be observed.

CONCLUSION:

The aptamer-siRNA compound can significantly induce K562 cell apoptosis, and provide reference for gene therapy of patients with chronic myelocytic lenkemia.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Apoptosis / Proliferación Celular Límite: Humans Idioma: Zh Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Apoptosis / Proliferación Celular Límite: Humans Idioma: Zh Año: 2015 Tipo del documento: Article