The janus kinases inhibitor AZD1480 attenuates growth of small cell lung cancers in vitro and in vivo
Journal
Clinical Cancer Research
Journal Volume
19
Journal Issue
24
Pages
6777-6786
Date Issued
2013
Author(s)
Abstract
Purpose: The prognosis of small cell lung cancer (SCLC) is poor, and there has been very little progress in the medical treatment of SCLC in the past two decades. We investigated the potential of Janus-activated kinases (JAK) inhibitor, AZD1480, for treatment of SCLC in vitro and in vivo. Experimental Design: JAK1 and JAK2 were inhibited by AZD1480 or siRNAs, and the effect of inhibition of JAK gene family on SCLC cell viability was evaluated. The effect of AZD1480 on cell-cycle distribution and apoptosis induction was studied. Antitumor effects of AZD1480 in tumor xenografts were assessed. Results: AZD1480 significantly inhibited growth of six out of 13 SCLC cells with IC50s ranging from 0.73 to 3.08 mmol/L. Knocking down of JAK2 and JAK1 inhibited proliferation of Jak2-positive/Jak1-negative H82 cells and Jak1-positive/Jak2-negative GLC4 cells, respectively. Treatment of SCLC cells with AZD1480 for 24 hours resulted in an increase of 4N DNA content and histone 3 serine 10 phosphorylation, indicative ofG2-Mphase arrest. Moreover, SCLCs underwent apoptosis after AZD1480 treatment as exemplified by the downregulation of MCL1, the accumulation of cleaved caspase 3, cleaved PARP, and increase of annexin-V- positive cells. Finally, xenograft experiments showed that AZD1480 attenuated the growth of H82 and GLC4 tumors in mice, and we observed stronger apoptosis as well as decreased CD31-positive endothelial cells in H82 and GLC4 xenografts upon AZD1480 treatment. Conclusions: JAK inhibitor AZD1480 attenuated growth of SCLC cells in vitro and in vivo. Clinical development of anti-JAKs therapies in SCLC warrants further investigation. ? 2013 American Association for Cancer Research.
SDGs
Other Subjects
5 chloro n2 [1 (5 fluoro 2 pyrimidinyl)ethyl] n4 (5 methyl 1h pyrazol 3 yl) 2,4 pyrimidinediamine; caspase 3; CD31 antigen; cisplatin; etoposide; histone H3; Janus kinase 1; Janus kinase 2; Janus kinase inhibitor; nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase; protein mcl 1; small interfering RNA; animal experiment; animal model; animal tissue; antiangiogenic activity; antiproliferative activity; apoptosis; article; cancer cell; cancer inhibition; controlled study; DNA content; down regulation; drug potentiation; endothelium cell; G2 phase cell cycle checkpoint; gene dosage; histone phosphorylation; IC 50; in vitro study; in vivo study; JAK2 gene; lung small cell cancer; mouse; nonhuman; priority journal; tumor xenograft; Animals; Apoptosis; Cell Line, Tumor; Cell Proliferation; Gene Expression Regulation, Neoplastic; Humans; Janus Kinase 1; Janus Kinase 2; Lung Neoplasms; Mice; Protein Kinase Inhibitors; Pyrazoles; Pyrimidines; Small Cell Lung Carcinoma; Xenograft Model Antitumor Assays
Type
journal article