Nejati-Koshki Kazem, Akbarzadeh Abolfazl, Pourhasan-Moghaddam Mohammad, Abhari Alireza, Dariushnejad Hassan
Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran E-mail :
Asian Pac J Cancer Prev. 2014 Jan;14(11):6595-9. doi: 10.7314/apjcp.2013.14.11.6595.
Leptin and its receptor are involved in breast carcinogenesis as mitogenic factors. Therefore, they could be considered as targets for breast cancer therapy. Expression of the leptin receptor gene could be modulated by leptin secretion. Silibinin and curcumin are herbal compounds with anti-cancer activity against breast cancer. The aim of this study was to assess their potential to inhibit of expression of the leptin gene and its receptor and leptin secretion. Cytotoxic effects of the two agents on combination on T47D breast cancer cells was investigated by MTT assay test after 24h treatment. With different concentrations the levels of leptin, leptin receptor genes expression were measured by reverse-transcription real-time PCR. Amount of secreted leptin in the culture medium was determined by ELISA. Data were statistically analyzed by one-way ANOVA test. The silibinin and curcumin combination inhibited growth of T47D cells in a dose dependent manner. There were also significant difference between control and treated cells in leptin expression and the quantity of secreted leptin with a relative decrease in leptin receptor expression. In conclusion, these herbal compounds inhibit the expression and secretion of leptin and it could probably be used as drug candidates for breast cancer therapy through leptin targeting in the future.
瘦素及其受体作为促有丝分裂因子参与乳腺癌的发生发展。因此,它们可被视为乳腺癌治疗的靶点。瘦素受体基因的表达可受瘦素分泌的调节。水飞蓟宾和姜黄素是具有抗乳腺癌活性的草药化合物。本研究的目的是评估它们抑制瘦素基因及其受体表达以及瘦素分泌的潜力。处理24小时后,通过MTT试验检测这两种药物联合使用对T47D乳腺癌细胞的细胞毒性作用。采用逆转录实时PCR法检测不同浓度下瘦素、瘦素受体基因的表达水平。通过ELISA法测定培养基中分泌的瘦素量。数据采用单因素方差分析进行统计学分析。水飞蓟宾和姜黄素联合使用以剂量依赖的方式抑制T47D细胞的生长。在瘦素表达、分泌的瘦素量以及瘦素受体表达相对降低方面,对照组和处理组细胞之间也存在显著差异。总之,这些草药化合物抑制瘦素的表达和分泌,未来可能通过靶向瘦素用作乳腺癌治疗的候选药物。