K562细胞
RAC1
生物
造血
白血病
细胞生物学
细胞生长
细胞培养
基因沉默
细胞
干细胞
免疫学
生物化学
基因
遗传学
信号转导
作者
Patrícia Favaro,Fabı́ola Traina,João Agostinho Machado‐Neto,Mariana Lazarini,Matheus Rodrigues Lopes,João Kleber Novais Pereira,Fernando Ferreira Costa,Elvira Infante,Anne J. Ridley,Sara Teresinha Olalla Saad
摘要
ABSTRACT The human FMNL1 is expressed predominantly in hematopoietic cells and has been described previously as overexpressed in hematopoietic malignancies. However, it is not known whether FMNL1 contributes to leukemogenesis. Here, we investigate the FMNL1 function using two different human leukemia models: Namalwa and K562 cell lines. FMNL1 depletion reduced cell proliferation and colony formation in both leukemic cell types, as well as a decrease in the tumor growth of FMNL1-depleted Namalwa cell xenografts. In addition, there was a decrease in migration and in TEM in FMNL1-depleted Namalwa cells. FMNL1 endogenously associates with Rac1, and FMNL1 silencing resulted in an increased Rac1 activity. The reduced migration observed in FMNL1-depleted cells was restored by inhibiting Rac activity. Our results indicate that FMNL1 stimulates leukemia cell proliferation as well as migration. This suggests that FMNL1 contributes to leukemogenesis and could act in part through Rac1 regulation.
科研通智能强力驱动
Strongly Powered by AbleSci AI