Orally active microtubule-targeting agent, MPT0B271, for the treatment of human non-small cell lung cancer, alone and in combination with erlotinib

A. C. Tsai, C. Y. Wang, J. P. Liou, H. C. Pai, C. J. Hsiao, J. Y. Chang, J. C. Wang, C. M. Teng, S. L. Pan

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

Microtubule-binding agents, such as taxanes and vinca alkaloids, are used in the treatment of cancer. The limitations of these treatments, such as resistance to therapy and the need for intravenous administration, have encouraged the development of new agents. MPT0B271 (N-[1-(4-Methoxy- benzenesulfonyl)-2,3-dihydro-1H-indol-7-yl]-1-oxy-isonicotinamide), an orally active microtubule-targeting agent, is a completely synthetic compound that possesses potent anticancer effects in vitro and in vivo. Tubulin polymerization assay and immunofluorescence experiment showed that MPT0B271 caused depolymerization of tubulin at both molecular and cellular levels. MPT0B271 reduced cell growth and viability at nanomolar concentrations in numerous cancer cell lines, including a multidrug-resistant cancer cell line NCI/ADR-RES. Further studies indicated that MPT0B271 is not a substrate of P-glycoprotein (P-gp), as determined by flow cytometric analysis of rhodamine-123 (Rh-123) dye efflux and the calcein acetoxymethyl ester (calcein AM) assay. MPT0B271 also caused G2/M cell-cycle arrest, accompanied by the up-regulation of cyclin B1, p-Thr161 Cdc2/p34, serine/threonine kinases polo-like kinase 1, aurora kinase A and B and the downregulation of Cdc25C and p-Tyr15 Cdc2/p34 protein levels. The appearance of MPM2 and the nuclear translocation of cyclin B1 denoted M phase arrest in MPT0B271-treated cells. Moreover, MPT0B271 induced cell apoptosis in a concentration-dependent manner; it also reduced the expression of Bcl-2, Bcl-xL, and Mcl-1 and increased the cleavage of caspase-3 and -7 and poly (ADP-ribose) polymerase (PARP). Finally, this study demonstrated that MPT0B271 in combination with erlotinib significantly inhibits the growth of the human non-small cell lung cancer A549 cells as compared with erlotinib treatment alone, both in vitro and in vivo. These findings identify MPT0B271 as a promising new tubulin-binding compound for the treatment of various cancers.

Original languageEnglish
Article numbere1162
JournalCell Death and Disease
Volume5
Issue number4
DOIs
Publication statusPublished - 2014

Fingerprint

Non-Small Cell Lung Carcinoma
Microtubules
Tubulin
Cyclin B1
Therapeutics
Neoplasms
Aurora Kinase B
Aurora Kinase A
CDC2 Protein Kinase
G2 Phase Cell Cycle Checkpoints
Vinca Alkaloids
Rhodamine 123
Caspase 7
Erlotinib Hydrochloride
N-(1-(4-methoxybenzenesulfonyl)-2,3-dihydro-1H-indol-7-yl)-1-oxyisonicotinamide
Cell Line
Taxoids
Poly(ADP-ribose) Polymerases
Protein-Serine-Threonine Kinases
P-Glycoprotein

Keywords

  • Apoptosis
  • Erlotinib
  • Microtubule-binding agents
  • Non-small cell lung cancer

ASJC Scopus subject areas

  • Cell Biology
  • Immunology
  • Cancer Research
  • Cellular and Molecular Neuroscience
  • Medicine(all)

Cite this

Orally active microtubule-targeting agent, MPT0B271, for the treatment of human non-small cell lung cancer, alone and in combination with erlotinib. / Tsai, A. C.; Wang, C. Y.; Liou, J. P.; Pai, H. C.; Hsiao, C. J.; Chang, J. Y.; Wang, J. C.; Teng, C. M.; Pan, S. L.

In: Cell Death and Disease, Vol. 5, No. 4, e1162, 2014.

Research output: Contribution to journalArticle

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AU - Pai, H. C.

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AU - Pan, S. L.

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