Cancer Treatment Reviews
Volume 36, Issue 6 , Pages 492-500, October 2010

Dasatinib: A potent SRC inhibitor in clinical development for the treatment of solid tumors

  • John Araujo

      Affiliations

    • Corresponding Author InformationCorresponding author. Address: Genitourinary Center, M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Unit 428, Houston, TX 77030, USA. Tel.: +1 713 792 2830; fax: +1 713 792 1654.
  • ,
  • Christopher Logothetis

      Affiliations

    • Tel.: +1 713 563 7210; fax: +1 713 792 1654.

Genitourinary Center, M.D. Anderson Cancer Centre, Houston, TX, USA

Received 22 December 2009; received in revised form 2 February 2010; accepted 6 February 2010. published online 12 March 2010.

Abstract 

SRC is a tyrosine kinase that plays a role in oncogenic, invasive and bone-metastatic processes. It has therefore been prioritized as a candidate therapeutic target in patients with solid tumors. Several SRC inhibitors are now in development, of which dasatinib has been most explored. Preclinical studies in a wide variety of solid tumor cell lines, including prostate, breast and glioma, have shown that that dasatinib acts as a cytostatic agent, inhibiting the processes of cell proliferation, invasion and metastasis. Dasatinib also inhibits the activity of osteoclasts, which have a major role in the development of metastatic bone lesions. Dasatinib has additive or synergistic activity in combination with a number of other agents, including cytotoxic agents and targeted therapies, providing a rationale for combination treatment in a clinical setting. Emerging clinical data with dasatinib support experimental observations, with preliminary phase 1 and 2 data demonstrating activity, both as a single agent and as combination therapy, in a range of solid tumors. Future clinical trials will further assess the clinical value of SRC inhibition with dasatinib.

Keywords: Dasatinib, SRC kinase, Solid tumors, Bone metastases, Preclinical, Phase 1 clinical trials, Phase 2 clinical trials

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PII: S0305-7372(10)00035-6

doi:10.1016/j.ctrv.2010.02.015

Cancer Treatment Reviews
Volume 36, Issue 6 , Pages 492-500, October 2010