Aberrant CDK9 expression within chordoma tissues and the therapeutic potential of a selective CDK9 inhibitor
Shen Shen1,2, Dylan C Dean2, Zujiang Yu1
1Precision Medicine Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, China.
Abstract:
Objectives: Chordomas are slow-growing malignancies that commonly affect vital neurological structures. These neoplasms are highly resistant to current chemotherapeutic regimens and often recur after surgical intervention. Therefore, there is an urgent need to identify molecular targets and more robust drugs to improve chordoma patient outcomes. It is well accepted that cyclin-dependent protein kinase 9 (CDK9) has tumorigenic roles in various cancers; however, the expression and significance of CDK9 in chordoma remains unknown. Methods: Expression of CDK9 in chordoma cell lines and tumor tissues was examined by Western blot and immunohistochemistry (IHC). The correlation between CDK9 expression in patient tissues and clinical prognosis was analyzed. The functional roles of CDK9 in chordoma were investigated after the addition of small interfering RNA (siRNA) and CDK9 inhibitor (LDC000067). Cell growth and proliferation were assessed with MTT and clonogenic assays. The effect of CDK9 inhibition on chordoma cells was further evaluated with a three-dimensional (3D) cell culture model which mimics the in vivo environment. Results: CDK9 was expressed in both chordoma cell lines and chordoma tissues. High- expression of CDK9 correlated with recurrence and poor outcomes for chordoma patients. CDK9 silencing with siRNA decreased growth and proliferation of chordoma cells and lowered levels of Mcl-1 and RNA polymerase II (RNAP II) phosphorylation. Pharmacological inhibition of CDK9 with the small molecular inhibitor LDC000067 reduced cell growth, supported apoptosis, suppressed cell colony formation in a clonogenic assay, and decreased spheroid growth in 3D culture. Conclusion: We demonstrate that CDK9 expression in chordoma correlates with patient outcome, and, when inhibited, chordoma cell growth and proliferation significantly decreases. Taken together, these results support CDK9 as an emerging potential target in chordoma therapy.
Insights
Cyclin-dependent protein kinase 9 (CDK9) is present in chordoma and linked to poor patient outcomes. Inhibiting CDK9 reduces chordoma cell growth and proliferation, suggesting it as a potential therapeutic target for this rare cancer.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Therapeutics
Background:
- Chordomas are rare, slow-growing bone cancers that frequently recur after surgery and are resistant to chemotherapy.
- There is a critical need for novel therapeutic targets and drugs to improve chordoma patient outcomes.
- The role of cyclin-dependent protein kinase 9 (CDK9) in chordoma tumorigenesis is currently unknown.
Purpose of the Study:
- To investigate the expression and functional significance of CDK9 in chordoma.
- To evaluate CDK9 as a potential therapeutic target for chordoma.
Main Methods:
- CDK9 expression was analyzed in chordoma cell lines and patient tissues using Western blot and immunohistochemistry (IHC).
- The impact of CDK9 inhibition via siRNA and a small molecule inhibitor (LDC000067) on chordoma cell growth, proliferation, apoptosis, and spheroid formation in 3D culture was assessed.
Main Results:
- CDK9 was expressed in chordoma cell lines and tissues, with high expression correlating with tumor recurrence and poor patient prognosis.
- CDK9 inhibition led to decreased chordoma cell growth, proliferation, and Mcl-1/RNAP II phosphorylation.
- Pharmacological inhibition of CDK9 reduced cell viability, promoted apoptosis, and inhibited colony and spheroid formation.
Conclusions:
- CDK9 expression is a significant biomarker for chordoma patient outcomes.
- Targeting CDK9 effectively inhibits chordoma cell growth and proliferation.
- CDK9 represents a promising therapeutic target for chordoma treatment.
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