Current status of SRC inhibitors in solid tumor malignancies
Open accessAbstract
Summary.: Src is believed to play an important role in cancer, and several agents targeting Src are in clinical development. Design.: We reviewed Src structure and function and preclinical data supporting its role in the development of cancer via a PubMed search. We conducted an extensive review of Src inhibitors by searching abstracts from major oncology meeting databases in the last 3 years and by comprehensively reviewing ongoing clinical trials on ClinicalTrials.gov. Results.: In this manuscript, we briefly review Src structure and function, mechanisms involving Src that lead to the development of cancer, and Src inhibitors and key preclinical data establishing a rationale for clinical application. We then focus on clinical data supporting their use in solid tumor malignancies, a newer arena than their more well-established hematologic applications. Particularly highlighted are clinical trials investigating new biomarkers as well as ongoing studies assessing Src inhibitor activity in biomarker-selected patient populations. We also review newer investigational Src-targeting agents. Conclusions.: Src inhibitors have shown little activity in monotherapy trials in unselected solid tumor patient populations. Combination studies and biomarker-driven clinical trials are under way.
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Preclinical evidence in sarcoma and ovarian cancer cell lines suggests that activation of Src reduces sensitivity to various chemotherapeutic drugs, including platinum agents, and that this resistance can be reversed by pharmacological inhibition.
“In addition, evidence from preclinical studies in sarcoma and ovarian cancer cell lines suggests that activation of Src reduces sensitivity to various chemotherapeutic drugs, including platinum agents, and that this resistance can be reversed by pharmacological inhibition [19, 20][21–23][24].”
From Dasatinib, a Src inhibitor, sensitizes liver metastatic colorectal carcinoma to oxaliplatin in tumors with high levels of phospho-Src (2016) · cites this paper as [24]
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References 116 · Cited by 158
- Authors
- Puls, L. N., Eadens, M., & Messersmith, W.
- Affiliations
- University of Colorado Cancer Center (US)
- Mayo Clinic (US)
- Corresponding author
- Messersmith, Wells
- ORCID
- Messersmith, Wells
- Venue
- The Oncologist
- Publisher
- Oxford University Press (OUP)
- Published
- 2011-04-26
- Volume
- 16
- Issue
- 5
- Pages
- 566-578
- ISSN
- 1083-7159 (ISSN-L)
- 1549-490X
- PMC
- PMC3228195
- OpenAlex
- W2108426094
- Cited by
- 158
- References
- 116
- Citations by year
- 2026: 3 · 2025: 12 · 2024: 5 · 2023: 10 · 2022: 7 · 2021: 6 · 2020: 17 · 2019: 12 · 2018: 6 · 2017: 11 · 2016: 17 · 2015: 10 · 2014: 18 · 2013: 14 · 2012: 8
- FWCI
- 1.70
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- The Oncologist (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Pfizer
- AstraZeneca
- Genentech
- 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
- Src kinase inhibitor, solid tumors, Src family kinases, clinical trials, biomarkers, combination therapy, hematologic malignancies
- MeSH terms
- Dasatinib, Aniline Compounds, Antineoplastic Agents, Antineoplastic Combined Chemotherapy Protocols, Clinical Trials as Topic, Dose-Response Relationship, Drug, Humans, Neoplasms, Nitriles, Pyrimidines, Quinazolines, Quinolines, Thiazoles, src-Family Kinases, Protein Kinase Inhibitors, Benzodioxoles
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