Picropodophyllin inhibits the growth of Ewing's sarcoma cells through the insulin‑like growth factor‑1 receptor/Akt signaling pathway.

Abstract

Ewing's sarcoma (ES) is the second most common type of pediatric bone tumor, and is associated with a poor prognosis. Picropodophyllin (PPP), a novel selective inhibitor of insulin‑like growth factor‑1 receptor (IGF‑1R), is able to strongly inhibit various types of cancers. However, the effect of IGF‑1R on ES remains unclear. Following treatment with various concentrations of PPP for various times, cell viability was determined using an MTT assay. In addition, cell proliferation and apoptosis was investigated separately by bromodeoxyuridine staining and flow cytometry, respectively. The PPP‑associated signaling pathway was also investigated. The results of the present study suggested that PPP inhibited cell proliferation and viability of A673 and SK‑ES‑1 human Ewing's sarcoma cells in a dose- and time‑dependent manner. In addition, cell apoptosis rates were increased following treatment with PPP. Further investigation of the underlying mechanism revealed that PPP inhibited Akt phosphorylation. Fumonisin B1, an Akt‑specific activator, reversed the inhibitory effects of PPP on cell growth. Furthermore, the results suggested that PPP decreased the expression levels of IGF‑1R, a common activator of Akt signaling. PPP inhibited the growth of human Ewing's sarcoma cells by targeting the IGF‑1R/Akt signaling pathway. Therefore, PPP may prove useful in the development of an effective strategy for the treatment of Ewing's sarcoma.

• Authors: Yong-Tao Wu, Bao-Jun Wang, Sheng-Wu Miao, Jian-Jun Gao
• Journal: Molecular medicine reports (Mol Med Rep) Vol. 12 Issue 5 Pg. 7045-50 (Nov 2015) ISSN: 1791-3004 [Electronic] Greece
• PMID: 26323364 (Publication Type: Journal Article)

Chemical References

• Antineoplastic Agents
• picropodophyllin
• Receptor, IGF Type 1
• Proto-Oncogene Proteins c-akt
• Podophyllotoxin

Topics

• Antineoplastic Agents (pharmacology)
• Apoptosis (drug effects)
• Bone Neoplasms (metabolism, pathology)
• Cell Line, Tumor
• Cell Proliferation (drug effects)
• Cell Survival (drug effects)
• Humans
• Phosphorylation (drug effects)
• Podophyllotoxin (analogs & derivatives, pharmacology)
• Proto-Oncogene Proteins c-akt (metabolism)
• Receptor, IGF Type 1 (metabolism)
• Sarcoma, Ewing (metabolism, pathology)
• Signal Transduction (drug effects)