Bosutinib (SKI-606) is an orally active Src and Abl kinase inhibitor presently in Phase III trials for treatment of chronic myelogenous leukaemia (CML), and in Phase II trials for treatment of breast cancer. Bosutinib is a potent antiproliferative and proapoptotic agent in CML cells and inhibits Bcr-Abl mediated signalling at nanomolar concentrations. Short-term administration of bosutinib causes regression of K562 and KU812 CML tumour xenografts. BaF3 murine myeloid cells expressing wild-type Bcr-Abl are sensitive to bosutinib treatment, as are BaF3 cells expressing many imatinib-resistant forms of Bcr-Abl. Recent studies indicate that bosutinib is active against a broader spectrum of kinases than originally believed. These additional inhibitory activities have interesting possibilities for further clinical development. This review will focus on preclinical studies supporting the clinical development of bosutinib for treatment of CML, with a discussion on the broader potential of this agent in other oncology indications. © 2010 Elsevier Ltd. All rights reserved

Boschelli, F., Arndt, K., Gambacorti-Passerini, C. (2010). Bosutinib: A review of preclinical studies in chronic myelogenous leukaemia. EUROPEAN JOURNAL OF CANCER, 46(10), 1781-1789 [10.1016/j.ejca.2010.02.032].

Bosutinib: A review of preclinical studies in chronic myelogenous leukaemia

Gambacorti-Passerini, C
2010

Abstract

Bosutinib (SKI-606) is an orally active Src and Abl kinase inhibitor presently in Phase III trials for treatment of chronic myelogenous leukaemia (CML), and in Phase II trials for treatment of breast cancer. Bosutinib is a potent antiproliferative and proapoptotic agent in CML cells and inhibits Bcr-Abl mediated signalling at nanomolar concentrations. Short-term administration of bosutinib causes regression of K562 and KU812 CML tumour xenografts. BaF3 murine myeloid cells expressing wild-type Bcr-Abl are sensitive to bosutinib treatment, as are BaF3 cells expressing many imatinib-resistant forms of Bcr-Abl. Recent studies indicate that bosutinib is active against a broader spectrum of kinases than originally believed. These additional inhibitory activities have interesting possibilities for further clinical development. This review will focus on preclinical studies supporting the clinical development of bosutinib for treatment of CML, with a discussion on the broader potential of this agent in other oncology indications. © 2010 Elsevier Ltd. All rights reserved
Articolo in rivista - Review Essay
Bcr-Abl; Bosutinib; Breast cancer; Chronic myelogenous leukaemia; Clinical trials; Imatinib resistance; SKI-606; Src; Tumour; Tyrosine kinase inhibitor; Aniline Compounds; Animals; Antineoplastic Agents; Cell Communication; Cell Line, Tumor; Clinical Trials as Topic; Cyclic N-Oxides; Drug Resistance, Neoplasm; Enzyme Inhibitors; Humans; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Mice; Neoplasm Transplantation; Nitriles; Protein Kinase Inhibitors; Quinolines; Transplantation, Heterologous; src-Family Kinases; Oncology; Cancer Research
English
2010
46
10
1781
1789
none
Boschelli, F., Arndt, K., Gambacorti-Passerini, C. (2010). Bosutinib: A review of preclinical studies in chronic myelogenous leukaemia. EUROPEAN JOURNAL OF CANCER, 46(10), 1781-1789 [10.1016/j.ejca.2010.02.032].
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/222943
Citazioni
  • Scopus 71
  • ???jsp.display-item.citation.isi??? 58
Social impact