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Metuzumab enhanced chemosensitivity and apoptosis in non-small cell lung carcinoma
Fei Feng1, Bin Wang1, Xiuxuan Sun1
1a National Translational Science Center for Molecular Medicine , Department of Cell Biology , Fourth Military Medical University , Xi'an , P.R. China.
Abstract:
Targeted therapeutics is used as an alternative treatment of non-small cell lung cancer (NSCLC); however, treatment effect is far from being satisfactory, and therefore identification of new targets is needed. We have previously shown that metuzumab inhibit tumor growth in vivo. The present study was performed to investigate the anti-tumor efficacy of metuzumab combined with gemcitabine and cisplatin (GP), paclitaxel and cisplatin (TP) or navelbine and cisplatin (NP) regimens in multiple NSCLC cell lines. Our results demonstrate that, in comparison to single agent metuzumab or GP treated cells, metuzumab combined with GP display inhibitory effects on tumor growth. Furthermore, we found that metuzumab elevated the sensitivity of cell lines to gemcitabine, which was identified by MTT assay. Flow cytometric analysis showed that metuzumab combined with gemcitabine (GEM) treatment led to an obvious G1 arrest and an elevated apoptosis in A549, NCI-H460 and NCI-H520 cells. Western blot analysis also demonstrated a significantly reduced level of cyclin D1, Bcl-2, and an obviously increase level of Bax and full-length caspase-3 in A549, NCI-H460 and NCI-H520 cells treated with metuzumab/gemcitabine combination in comparison with single agent treated cells. In addition, metuzumab/gemcitabine treated A549, NCI-H460 and NCI-H520 cells also demonstrated a significantly increase in deoxycytidine kinase (dCK) protein level compared with single agent metuzumab or gemcitabine treated cells. Xenograft models also demonstrated that this metuzumab/gemcitabine combination led to upregulation of dCK. Taken together, the mechanisms of metuzumab combined with GP repress tumor growth were that the combined treatment significantly inhibited the tumor cell proliferation, apoptosis and cell cycle in vitro and in vivo and at least partially by induction of dCK expression. Our results suggested that metuzumab could significantly enhance chemosensitivity of human NSCLC cells to gemcitabine. Metuzumab/gemcitabine combination treatment may be a potentially useful therapeutic regimen for NSCLC patients.
Insights
Metuzumab enhances gemcitabine efficacy in non-small cell lung cancer (NSCLC) by increasing apoptosis and cell cycle arrest. This combination therapy shows potential for treating NSCLC patients.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Non-small cell lung cancer (NSCLC) treatment requires novel therapeutic targets.
- Metuzumab has demonstrated in-vivo tumor growth inhibition.
- Current targeted therapies for NSCLC have limitations.
Purpose of the Study:
- To investigate the anti-tumor efficacy of metuzumab combined with gemcitabine, paclitaxel, or navelbine regimens in NSCLC.
- To elucidate the mechanisms underlying the anti-tumor effects of metuzumab and gemcitabine combination therapy.
- To evaluate the potential of metuzumab as a chemosensitizer for NSCLC.
Main Methods:
- In-vitro studies using multiple NSCLC cell lines (A549, NCI-H460, NCI-H520).
- MTT assays to assess cell viability and drug sensitivity.
- Flow cytometry for cell cycle analysis and apoptosis detection.
- Western blot analysis for protein expression levels (cyclin D1, Bcl-2, Bax, caspase-3, dCK).
- In-vivo xenograft models to validate findings.
Main Results:
- Metuzumab combined with gemcitabine (GP regimen) showed superior tumor growth inhibition compared to single agents.
- Metuzumab significantly enhanced NSCLC cell sensitivity to gemcitabine.
- The combination induced G1 cell cycle arrest and elevated apoptosis.
- Key proteins involved in apoptosis and cell cycle regulation were modulated.
- Upregulation of deoxycytidine kinase (dCK) was observed in vitro and in vivo.
Conclusions:
- Metuzumab combined with gemcitabine demonstrates significant anti-tumor efficacy in NSCLC through inhibition of proliferation, apoptosis, and cell cycle.
- The combination therapy's mechanism involves, at least partially, the induction of dCK expression.
- Metuzumab shows potential to enhance chemosensitivity to gemcitabine in human NSCLC.
- Metuzumab/gemcitabine combination represents a promising therapeutic strategy for NSCLC patients.
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