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Oncotarget. 2014 Sep 30;5(18):8379-92.

Picropodophyllin causes mitotic arrest and catastrophe by depolymerizing microtubules via insulin-like growth factor-1 receptor-independent mechanism.

Author information

1
Department of Oncology-Pathology, Cancer Center Karolinska, Solna, Sweden.
2
Department of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden.
3
Axelar AB, Karolinska Institutet Science Park, Solna, Sweden.
4
Department of Clinical Chemistry, Karolinska Institutet, Stockholm, Sweden.
5
Department of Oncology-Pathology, Cancer Center Karolinska, Solna, Sweden. Alexandria University, Faculty of Science, Department of Zoology, Alexandria, Egypt. The Ronald A. Matricaria Institute of Molecular Medicine at Phoenix Children's Hospital, University of Arizona College of Medicine-Phoenix, Department of Child Health, Phoenix, Arizona, USA.

Abstract

Picropodophyllin (PPP) is an anticancer drug undergoing clinical development in NSCLC. PPP has been shown to suppress IGF-1R signaling and to induce a G2/M cell cycle phase arrest but the exact mechanisms remain to be elucidated. The present study identified an IGF-1-independent mechanism of PPP leading to pro-metaphase arrest. The mitotic block was induced in human cancer cell lines and in an A549 xenograft mouse but did not occur in normal hepatocytes/mouse tissues. Cell cycle arrest by PPP occurred in vitro and in vivo accompanied by prominent CDK1 activation, and was IGF-1R-independent since it occurred also in IGF-1R-depleted and null cells. The tumor cells were not arrested in G2/M but in mitosis. Centrosome separation was prevented during mitotic entry, resulting in a monopolar mitotic spindle with subsequent prometaphase-arrest, independent of Plk1/Aurora A or Eg5, and leading to cell features of mitotic catastrophe. PPP also increased soluble tubulin and decreased spindle-associated tubulin within minutes, indicating that it interfered with microtubule dynamics. These results provide a novel IGF-1R-independent mechanism of antitumor effects of PPP.

PMID:
25268741
PMCID:
PMC4226690
DOI:
10.18632/oncotarget.2292
[Indexed for MEDLINE]
Free PMC Article

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