Dang Qiang, Song Wenbin, Xu Defeng, Ma Yanmin, Li Feng, Zeng Jin, Zhu Guodong, Wang Xinyang, Chang Luke S, He Dalin, Li Lei
Department of Urology, The First Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Xi'an, PR, China.
School of Pharmaceutical and Life Sciences, Changzhou University, Changzhou, Jiangsu, PR, China.
Mol Carcinog. 2015 Sep;54(9):831-40. doi: 10.1002/mc.22154. Epub 2014 Apr 2.
The effects of the flavonoid compound, kaempferol, which is an inhibitor of cancer cell proliferation and an inducer of cell apoptosis have been shown in various cancers, including lung, pancreatic, and ovarian, but its effect has never been studied in bladder cancer. Here, we investigated the effects of kaempferol on bladder cancer using multiple in vitro cell lines and in vivo mice studies. The MTT assay results on various bladder cancer cell lines showed that kaempferol enhanced bladder cancer cell cytotoxicity. In contrast, when analyzed by the flow cytometric analysis, DNA ladder experiment, and TUNEL assay, kaempferol significantly was shown to induce apoptosis and cell cycle arrest. These in vitro results were confirmed in in vivo mice studies using subcutaneous xenografted mouse models. Consistent with the in vitro results, we found that treating mice with kaempferol significant suppression in tumor growth compared to the control group mice. Tumor tissue staining results showed decreased expressions of the growth related markers, yet increased expressions in apoptosis markers in the kaempferol treated group mice tissues compared to the control group mice. In addition, our in vitro and in vivo data showed kaempferol can also inhibit bladder cancer invasion and metastasis. Further mechanism dissection studies showed that significant down-regulation of the c-Met/p38 signaling pathway is responsible for the kaempferol mediated cell proliferation inhibition. All these findings suggest kaempferol might be an effective and novel chemotherapeutic drug to apply for the future therapeutic agent to combat bladder cancer.
黄酮类化合物山奈酚具有抑制癌细胞增殖和诱导细胞凋亡的作用,已在包括肺癌、胰腺癌和卵巢癌在内的多种癌症中得到证实,但其对膀胱癌的作用尚未见研究报道。在此,我们利用多种体外细胞系和体内小鼠实验研究了山奈酚对膀胱癌的影响。对多种膀胱癌细胞系的MTT实验结果显示,山奈酚增强了膀胱癌细胞的细胞毒性。相反,通过流式细胞术分析、DNA梯状条带实验和TUNEL检测分析发现,山奈酚显著诱导细胞凋亡和细胞周期阻滞。这些体外实验结果在皮下异种移植小鼠模型的体内小鼠实验中得到了证实。与体外实验结果一致,我们发现与对照组小鼠相比,用山奈酚治疗的小鼠肿瘤生长受到显著抑制。肿瘤组织染色结果显示,与对照组小鼠相比,山奈酚治疗组小鼠组织中生长相关标志物的表达降低,而凋亡标志物的表达增加。此外,我们的体外和体内数据表明,山奈酚还可以抑制膀胱癌的侵袭和转移。进一步的机制剖析研究表明,c-Met/p38信号通路的显著下调是山奈酚介导的细胞增殖抑制的原因。所有这些发现表明,山奈酚可能是一种有效且新型的化疗药物,有望成为未来对抗膀胱癌的治疗药物。