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薄荷醇通过人类膀胱癌 T24 细胞系中的 TRPM8 通道诱导细胞死亡。

Menthol induces cell death via the TRPM8 channel in the human bladder cancer cell line T24.

机构信息

Graduate School, Southern Medical University, Guangzhou, China.

出版信息

Oncology. 2009;77(6):335-41. doi: 10.1159/000264627. Epub 2009 Dec 2.

Abstract

OBJECTIVE

Growing evidence has shown that menthol has potent anticancer activity in various human cancers via the transient receptor potential melastatin 8 (TRPM8)-dependent pathway or in a TRPM8-independent manner. However, its effect on bladder cancer remains obscure. In the present investigation, we examined the expression of TRPM8 and the role of menthol in cells of the human bladder cancer cell line T24.

METHODS

RT-PCR, Western blotting and immunocytochemistry were used to confirm the expression and location of TRPM8 in T24 cells.

RESULTS

TRPM8 was highly expressed in T24 cells and located in both the cell membrane and cytoplasm. With the use of small interfering RNA to silence the expression of TRPM8, we found that menthol could increase the concentration of intracellular calcium and decrease cell viability via the TRPM8 channel in T24 cells. We also found that menthol could induce cell death through TRPM8 in T24 cells, rather than cell cycle arrest or apoptosis. Moreover, the detection of mitochondrial membrane potential showed that menthol could induce mitochondrial membrane depolarization in T24 cells.

CONCLUSIONS

In the present study, we demonstrated that menthol can induce mitochondrial membrane depolarization via the TRPM8 channel in cells of the human bladder cancer cell line T24, resulting in cell death. It would be helpful to explore the precise mechanism of action of menthol in bladder cancer with a view to its possible use as intravesical chemotherapy.

摘要

目的

越来越多的证据表明,薄荷醇通过瞬时受体电位 melastatin 8(TRPM8)依赖性途径或以 TRPM8 非依赖性方式在各种人类癌症中具有强大的抗癌活性。然而,其对膀胱癌的影响尚不清楚。在本研究中,我们研究了 TRPM8 的表达以及薄荷醇在人膀胱癌 T24 细胞中的作用。

方法

使用 RT-PCR、Western blotting 和免疫细胞化学来确认 T24 细胞中 TRPM8 的表达和位置。

结果

TRPM8 在 T24 细胞中高表达,位于细胞膜和细胞质中。使用小干扰 RNA 沉默 TRPM8 的表达,我们发现薄荷醇可以通过 T24 细胞中的 TRPM8 通道增加细胞内钙离子浓度并降低细胞活力。我们还发现薄荷醇可以通过 TRPM8 诱导 T24 细胞死亡,而不是细胞周期停滞或细胞凋亡。此外,线粒体膜电位的检测表明,薄荷醇可以诱导 T24 细胞中线粒体膜去极化。

结论

在本研究中,我们证明薄荷醇可以通过 T24 细胞中的 TRPM8 通道诱导线粒体膜去极化,导致细胞死亡。这有助于探索薄荷醇在膀胱癌中的精确作用机制,以期将其用作膀胱内化疗。

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