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Effects of Src kinase inhibition by saracatinib (AZD0530) on bone turnover in advanced malignancy in a Phase I study
Rosemary A Hannon1, Richard D Finkelman, Glen Clack
1Academic Unit of Bone Metabolism, University of Sheffield, Sheffield, UK.
Abstract:
Saracatinib (AZD0530) is an orally active once-daily Src kinase inhibitor which modulates key signaling pathways in cancer cells. In a Phase I study in patients with advanced solid malignancies resistant to standard treatment we assessed the effect of saracatinib on bone turnover. Fifty-one patients were randomized into three parallel groups to receive saracatinib 50, 125 or 175 mg/day. After a single dose followed by a 7-day washout, patients received once-daily doses for 21 days. Bone turnover markers were measured in serum and urine samples collected before dosing on days 1, 2, 3, 17 and 28. Samples were available at baseline and more than one other time point for 44 patients. Bone resorption markers were significantly decreased by saracatinib. Serum cross-linked C-terminal telopeptide of type I collagen (sCTX) changed in the 50, 125 and 175 mg/day groups by -36% (95% CI -58, -4), -64% (95% CI -75, -48) and -75% (95% CI -83, -61), respectively, at day 28. Urinary cross-linked N-terminal telopeptide of type I collagen/creatinine ratio (uNTX/Cr) changed in the 50, 125 and 175 mg/day groups by; -13% (95% CI -33, 13), -48% (95% CI -59, -34) and -50% (95% CI -62, -35), respectively, at day 28. The significant decreases in bone resorption markers indicate that suppression of Src kinase inhibits osteoclast activity in patients with advanced cancer. This result suggests that saracatinib may have therapeutic benefit in metastatic bone disease.
Insights
Saracatinib, a Src kinase inhibitor, significantly reduced bone resorption markers in patients with advanced cancer. This suggests potential therapeutic benefits for metastatic bone disease by inhibiting osteoclast activity.
Area of Science:
- Oncology
- Pharmacology
- Bone Biology
Background:
- Saracatinib (AZD0530) is an oral Src kinase inhibitor targeting cancer cell signaling pathways.
- Advanced solid malignancies often present challenges with standard treatments and can involve bone complications.
Purpose of the Study:
- To assess the impact of saracatinib on bone turnover in patients with advanced solid malignancies.
- To evaluate the dose-dependent effect of saracatinib on bone resorption markers.
Main Methods:
- Phase I study involving 51 patients with advanced solid malignancies.
- Randomized administration of saracatinib at 50, 125, or 175 mg/day.
- Measurement of serum (sCTX) and urinary (uNTX/Cr) bone turnover markers at multiple time points.
Main Results:
- Saracatinib significantly decreased bone resorption markers in a dose-dependent manner.
- Serum cross-linked C-terminal telopeptide of type I collagen (sCTX) decreased by -36% to -75% at day 28 across dosage groups.
- Urinary cross-linked N-terminal telopeptide of type I collagen/creatinine ratio (uNTX/Cr) decreased by -13% to -50% at day 28 across dosage groups.
Conclusions:
- Suppression of Src kinase by saracatinib inhibits osteoclast activity.
- Saracatinib demonstrates potential therapeutic value in managing metastatic bone disease.
- Further investigation into saracatinib for bone-related complications in cancer is warranted.
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