Cited by 244Cancer Mechanisms and TherapyProtein Kinase Regulation and GTPase SignalingLung Cancer Treatments and Mutations

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

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Araujo, John, Logothetis, Christopher·2010·Cancer Treatment Reviews

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.

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Crossref · 10.1016/j.ctrv.2010.02.015

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  • Dasatinib and bosutinib have anticancer activity against NSCLC.

    “Dasatinib and bosutinib have anticancer activity against NSCLC (72, 73).”

    From SRC kinase drives multidrug resistance induced by KRAS-G12C inhibition (2024) · cites this paper as [72]

    The Preclinical activity section reports that dasatinib inhibited proliferation of NSCLC cell lines. The Phase 2 section also reports a partial response in one of 16 patients with metastatic NSCLC. These passages support activity for dasatinib, but our copy does not establish the claim for bosutinib. (LLM, conf=0.88)

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References 91 · Cited by 244

Research works printed but not linked: 1

  1. [55]Luo FR Camuso A McGlinchey K Evaluation of anti-osteoclastic activity of the novel, oral multi-targeted kinase inhibitor dasatinib (BMS-354825) Proceedings of the Molecular Targets and Cancer Therapeutics meeting 2005 173 abstract B178

Authors
Araujo, J., & Logothetis, C.
Affiliations
The University of Texas MD Anderson Cancer Center (US)
Corresponding author
  • Araujo, John
  • Logothetis, Christopher
Venue
Cancer Treatment Reviews
Publisher
Elsevier BV
Published
2010-10
Volume
36
Issue
6
Pages
492-500
ISSN
0305-7372 (ISSN-L)
OpenAlex
W2000868207
Cited by
244
References
91
Citations by year
2026: 11 · 2025: 23 · 2024: 17 · 2023: 17 · 2022: 15 · 2021: 9 · 2020: 25 · 2019: 18 · 2018: 8 · 2017: 11 · 2016: 10 · 2015: 15 · 2014: 9 · 2013: 11 · 2012: 13
FWCI
2.18
Type
journal article
Language
en
Open access
Locations
  • Cancer Treatment Reviews (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • Yale University
  • National Cancer Institute (P01CA095616)
Topics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Cancer Mechanisms and Therapy
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Treatments and Mutations
Keywords
dasatinib, Src kinase inhibitor, solid tumors, tyrosine kinase, metastasis, bone metastasis, osteoclast inhibition, combination therapy, prostate cancer, breast cancer, glioma, cell proliferation, clinical development
MeSH terms
Dasatinib, Animals, Antineoplastic Agents, Clinical Trials as Topic, Humans, Neoplasms, Pyrimidines, Thiazoles, src-Family Kinases, Protein Kinase Inhibitors

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