Function of MEIS1 and miR-425 to the Regulating of Chronic Myeloid Leukemia Cell Proliferation / 中国实验血液学杂志
Journal of Experimental Hematology
; (6): 802-807, 2020.
Article
en Zh
| WPRIM
| ID: wpr-829040
Biblioteca responsable:
WPRO
ABSTRACT
OBJECTIVE@#To investigate the function and mechanism of transcription factor of MEIS1 and miR-425 to the proliferation of chronic myeloid leukemia cell K562.@*METHODS@#Bioinformatic prediction was used to analyze the binding of MEIS1 in miR-425 promoter region. ChIP-qPCR coupled with dual luciferase assay was used to detect the combination of MEIS1 and the transcription activity of miR-425, and its regulative role in the transcription activity miR-425. CCK-8 was used to detect the effect of MEIS1 and miR-425 on cell proliferation. Flow cytometry with PI staining was used to detected the effect of MEIS1 and miR-425 on K562 cell cycle progression. Western blot was used to examine the effect of miR-452 on the expression level of MEIS1.@*RESULTS@#MEIS1 could bind the promoter of miR-425 and repressed its transcription. After K562 was transfected by shRNA, the K562 cell proliferation and cell cycle progression was significantly inhibitied. Moreover, after K562 cells were transfected by miR-425 mimic, cell proliferation and cell cycle was inhibited. The expression level of MEIS1 could be inhibited by the combination of miR-425 and MEIS1 3'UTR.@*CONCLUSION@#MEIS1 can inhibit the activity of miR-425 in transcriptional level, while the miR-425 can suppress the expression of MEIS1 protein in post-transnational level. Therefore, a regulatory circuit comprising from MEIS1 and miR-425 regulates K562 cell proliferation.
Texto completo:
1
Banco de datos:
WPRIM
Asunto principal:
Leucemia Mielógena Crónica BCR-ABL Positiva
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Apoptosis
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Células K562
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MicroARNs
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Proliferación Celular
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Proteína 1 del Sitio de Integración Viral Ecotrópica Mieloide
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Genética
Tipo de estudio:
Prognostic_studies
Límite:
Humans
Idioma:
Zh
Año:
2020
Tipo del documento:
Article