Dasatinib: A potent SRC inhibitor in clinical development for the treatment of solid tumors
Open accessAbstract
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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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
- [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)
- PMC
- PMC3940067
- 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
- green
- www.ncbi.nlm.nih.gov
- 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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