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Generation of Prostate Cancer Cell Models of Resistance to the Anti-mitotic Agent Docetaxel
Published on: September 8, 2017
Cyclosporine A Decreased Paclitaxel Resistance in Prostate Cancer Cells by Inhibiting MTDH Expression
Jiangtao Li1, Yuzhi Li1, Xiaohong Zhang2
1Department of Urinary Surgery, Hebei Eighth People's Hospital, Shijiazhuang, China.
Abstract:
This study aims to investigate the effect and mechanism of cyclosporine A (CsA) on paclitaxel-resistant prostate cancer cells. Paclitaxel-resistant prostate cancer cell lines were established by gradual increment method. The proliferation of cells was tested using MTT and colony formation assay. Western blot was used to detect protein expression. Expression levels of gene mRNA were detected using real-time polymerase chain reaction (RT-PCR). Xenografts in nude mice were used to validate the conclusion in vitro. The results showed that CsA could increase the sensitivity of prostate cancer cells to paclitaxel. Treatment of paclitaxel-resistant prostate cancer cell lines with CsA gradients decreased metadherin (MTDH) protein expression. RT-PCR showed that CsA could decrease the mRNA level of MTDH. Overexpression of MTDH in prostate cancer cells increases paclitaxel resistance in prostate cancer cells. Conversely, knockdown of MTDH reduced paclitaxel resistance in prostate cancer cells. Treating cells with CsA failed to reduce paclitaxel resistance in prostate cancer cells when MTDH was overexpressed. Xenografts in nude mice yielded consistent conclusions with the in vitro results. In conclusion, CsA can reduce the resistance of prostate cancer cells to paclitaxel. In vitro and in vivo experiments have shown that CsA can reduce paclitaxel resistance in prostate cancer cells by decreasing MTDH expression. In clinical practice, CsA can be used in combination with paclitaxel to improve the therapeutic effect on prostate cancer. MTDH may serve as a novel target for treating paclitaxel resistance in prostate cancer.
Insights
Cyclosporine A (CsA) enhances paclitaxel effectiveness against prostate cancer by reducing metadherin (MTDH) expression. This finding suggests CsA as a potential therapeutic agent to overcome paclitaxel resistance in prostate cancer treatment.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Prostate cancer often develops resistance to paclitaxel, a key chemotherapy drug.
- Understanding the mechanisms of paclitaxel resistance is crucial for improving treatment outcomes.
Purpose of the Study:
- To investigate the effect of cyclosporine A (CsA) on paclitaxel-resistant prostate cancer.
- To elucidate the underlying mechanism of CsA's action, focusing on metadherin (MTDH).
Main Methods:
- Established paclitaxel-resistant prostate cancer cell lines.
- Utilized MTT assays, colony formation assays, Western blot, and RT-PCR.
- Validated findings through in vivo xenograft models in nude mice.
Main Results:
- CsA treatment increased prostate cancer cell sensitivity to paclitaxel.
- CsA decreased both protein and mRNA expression of metadherin (MTDH).
- MTDH overexpression correlated with increased paclitaxel resistance; MTDH knockdown reduced resistance.
Conclusions:
- CsA effectively reduces paclitaxel resistance in prostate cancer cells by downregulating MTDH expression.
- MTDH is identified as a potential therapeutic target for overcoming paclitaxel resistance.
- CsA holds promise for combination therapy with paclitaxel to enhance prostate cancer treatment efficacy.
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