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Isolation of Cancer Stem Cells From Human Prostate Cancer Samples
Published on: March 14, 2014
Combination Effect of Bowman-Birk Inhibitor and α-Tocopheryl Succinate on Prostate Cancer Stem-Like Cells
Saki Kaneko1, Takumi Yamazaki2, Kakeru Kohno1,3
1Graduate School of Food and Nutritional Sciences, Toyo University.
Abstract:
The reoccurrence of androgen-dependent prostate cancer after anti-androgen therapy mainly depends on prostate cancer stem-like cells. To reduce the risk, it is important to delete the cancer stem-like cells. Furthermore, to induce differentiation of cancer stem-like cells is critical to abrogate stemness of the cells. Therefore, we tried to investigate a possibility on the establishment of a new effective therapy to eradicate the cancer stem-like cells via the induction of differentiation in this study. Prostate cancer stem-like cells from an androgen-dependent prostate cancer cell line (LNCaP cell) had severe resistance against an anti-androgen therapeutic agent. We selected Bowman-Birk inhibitor (BBI) from soybeans reported as a chemopreventive agent in prostate cancer to differentiate the caner stem-like cells and α-tocopheryl succinate (TOS) known as a mitocan to induce effectively cytotoxic effect against the cancer stem-like cells. In fact, only TOS treatment had cytotoxic effect against the cancer stem-like cells, but the addition of BBI treatment to the cells treated with TOS reinforced TOS-mediated cytotoxicity in the cancer stem-like cells. This reinforcement coincided with the combination-enhanced apoptosis in the stem-like cells. Also, we confirmed caspase9-caspase3 cascade mainly contributed to the enhancement of the cytotoxicity in the stem-like cells caused by the combination, indicating that the reinforcement of BBI on TOS-mediated apoptosis via mitochondria related to the enhancing cytotoxic effect of the combination on the prostate cancer stem-like cells. Overall, it seems that the combination is an effective new approach to reduce the reoccurrence of prostate cancer targeting prostate cancer stem cells.
Insights
This study explores a new therapy combining Bowman-Birk inhibitor (BBI) and α-tocopheryl succinate (TOS) to target prostate cancer stem cells. The combination enhances the cytotoxic effect of TOS, potentially reducing cancer recurrence.
Area of Science:
- Oncology
- Cancer Stem Cell Biology
- Pharmacology
Background:
- Prostate cancer recurrence after anti-androgen therapy is linked to resistant cancer stem-like cells.
- Eradicating or inducing differentiation of these stem cells is crucial for effective treatment.
- Androgen-dependent prostate cancer stem cells exhibit significant resistance to anti-androgen agents.
Purpose of the Study:
- To investigate a novel therapeutic strategy targeting prostate cancer stem-like cells.
- To evaluate the combination of Bowman-Birk inhibitor (BBI) and α-tocopheryl succinate (TOS) for eradicating these cells.
- To induce differentiation and enhance cytotoxicity in prostate cancer stem cells.
Main Methods:
- Utilized LNCaP cells, an androgen-dependent prostate cancer cell line.
- Treated cancer stem-like cells with TOS alone and in combination with BBI.
- Assessed cytotoxicity, apoptosis, and the caspase9-caspase3 cascade.
Main Results:
- TOS demonstrated cytotoxic effects on cancer stem-like cells.
- The addition of BBI significantly reinforced TOS-mediated cytotoxicity.
- Combination treatment led to enhanced apoptosis, primarily through the caspase9-caspase3 pathway.
Conclusions:
- The combination of BBI and TOS is a promising approach to enhance the eradication of prostate cancer stem-like cells.
- This strategy targets the mitochondria-related apoptosis pathway, offering a new avenue for reducing prostate cancer recurrence.
- Targeting prostate cancer stem cells with this combination therapy shows potential for improved treatment outcomes.
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