Journal of Bioenergetics and Biomembranes

, Volume 49, Issue 6, pp 437–443 | Cite as

Antibiotic anisomycin induces cell cycle arrest and apoptosis through inhibiting mitochondrial biogenesis in osteosarcoma

Article

Abstract

The anti-cancer activities of antibiotic anisomycin have been demonstrated in kidney, colon and ovarian cancers whereas its underlying mechanisms are not well elucidated. In this work, we investigated whether anisomycin is effective in sensitizes osteosarcoma cell response to chemotherapy. We show that anisomycin inhibits proliferation via inducing osteosarcoma cell arrest at G2/M phase, accompanied by the increased levels of mitotic marker cyclin B and the decreased levels of Rb and E2F-1. Anisomycin also induces apoptosis in a caspase-dependent manner in osteosarcoma cells. Importantly, anisomycin is less effective in normal control NIH3T3 cells compared to osteosarcoma cells. In addition, anisomycin inhibits osteosarcoma growth in xenograft mouse model and enhances the inhibitory effects of doxorubicin in osteosarcoma in vitro and in vivo. Mechanistically, anisomycin targets mitochondrial biogenesis in osteosarcoma as shown by the decreased mitochondrial membrane potential, suppressed mitochondrial respiration via decreasing complex I activity, reduced ATP production. Furthermore, mitochondrial biogenesis stimulator acetyl-L-Carnitine (ALCAR) significantly rescues the inhibitory effects of anisomycin in osteosarcoma cells. Our work demonstrates that anisomycin is active against osteosarcoma cells and the molecular mechanism of its action is the inhibition of mitochondrial biogenesis.

Keywords

Anisomycin Mitochondria biogenesis Osteosarcoma 

Notes

Acknowledgements

This work was supported by a research grant provided by Xiangyang Central Hospital (201416081869).

Compliance with ethical standards

Conflicts of interest

All authors declare no conflicts of interest.

Supplementary material

10863_2017_9734_MOESM1_ESM.doc (32 kb)
Supplementary Fig. S1 (DOC 32 kb)

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2017

Authors and Affiliations

  1. 1.Department of Oncology, The Affiliated Hospital of Hubei University of Arts and ScienceXiangyang Central HospitalXiangyangPeople’s Republic of China
  2. 2.Department of Oncology, Taihe HospitalHubei University of MedicineShiyanPeople’s Republic of China

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