Purpose. This study aims to determine the influence of targeting araC-resistant acute myeloid leukemia by dual inhibition cyclin-dependent protein kinase (CDK9) and B-cell lymphoma-2 (Bcl-2). Method. The c-Myc inhibitor 10058-F4 and the CDK9 inhibitor AZD4573 were used to determine the cell cycle arrest and apoptosis. Results. 10058-F4 reduces c-Myc protein levels and suppresses HepG2 cell proliferation, possibly by upregulating cyclin-dependent kinase (CDK) inhibitors, p21WAF1, and reducing intracellular alpha-fetal protein (AFP) levels. Conclusion. The combination of AZD4573 and 10058-F4 has a synergistic anti-araC-resistant AML activity, providing a solid database for the aforementioned scientific hypothesis.
第一作者单位:[1]China Japan Friendship Hosp, Dept Lab Med, Beijing, Peoples R China
通讯作者:
推荐引用方式(GB/T 7714):
Li Linzhang,Han Chengwu,Yu Xueying,et al.Targeting AraC-Resistant Acute Myeloid Leukemia by Dual Inhibition of CDK9 and Bcl-2: A Systematic Review and Meta-Analysis[J].JOURNAL of HEALTHCARE ENGINEERING.2022,2022:doi:10.1155/2022/2842066.
APA:
Li, Linzhang,Han, Chengwu,Yu, Xueying,Shen, Jun&Cao, Yongtong.(2022).Targeting AraC-Resistant Acute Myeloid Leukemia by Dual Inhibition of CDK9 and Bcl-2: A Systematic Review and Meta-Analysis.JOURNAL of HEALTHCARE ENGINEERING,2022,
MLA:
Li, Linzhang,et al."Targeting AraC-Resistant Acute Myeloid Leukemia by Dual Inhibition of CDK9 and Bcl-2: A Systematic Review and Meta-Analysis".JOURNAL of HEALTHCARE ENGINEERING 2022.(2022)