Luo Gang, Zeng Yun, Zhu Ling, Zhang Yi-xian, Zhou Li-ming
Department of Pharmacology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu 610041, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2009 May;40(3):449-53.
To investigate inhibition effect and its mechanism of Nobiletin on the proliferation of lung cancer cells in vivo and in vitro.
Human lung adenocarcinoma cell line A549 was treated with various dose of Nobiletin, and cell proliferation was tested by MTT assay. DNA damage of A549 cells was detected by comet assay. Expression of Bcl-2 and Bax proteins were analyzed by Western blot assay. Lewis lung carcinoma (LLC) models were established in C57BL/6 mice and treated with Nobiletin once a day for 12 d, and then the inhibitory rate of tumor growth was measured. Cellular apoptosis was determined using TUNEL assay. The protein levels of Bax, Bcl-2 and Caspase-9 in LLC tissues were determined by immunohistochemistry.
The treatment of Nobiletin resulted in significant inhibition of A549 cells proliferation in a dose-dependent manner. Comet assay revealed that DNA damage increased along with the increase of Nobiletin dosage. Western blot analysis showed that A549 cells pretreated with Nobiletin had Bcl-2 protein expression decreased and Bax protein expression increased. The inhibitory rates of lung carcinoma were 43.70%, 27.59% and 20.14% in lewis mice treated with high (300 mg/kg), middle (200 mg/kg), and low (100 mg/kg) dosage of Nobiletin (P<0.01). With the treatment of Nobiletin, the expression of Bax and Caspase-9 proteins increased, and the expression of Bcl-2 proteins decreased.
Nobiletin has certain inhibitory effects on the proliferation of lung cancer cells both in vivo and in vitro. The mechanism may be related to up-regulation of Bax and Caspase-9 and down-regulation of Bcl-2.
研究诺米林对肺癌细胞体内外增殖的抑制作用及其机制。
用不同剂量的诺米林处理人肺腺癌细胞系A549,采用MTT法检测细胞增殖情况。用彗星试验检测A549细胞的DNA损伤。采用蛋白质免疫印迹法分析Bcl-2和Bax蛋白的表达。在C57BL/6小鼠中建立Lewis肺癌(LLC)模型,每天用诺米林处理12天,然后测量肿瘤生长抑制率。采用TUNEL法检测细胞凋亡。用免疫组织化学法检测LLC组织中Bax、Bcl-2和Caspase-9的蛋白水平。
诺米林处理可显著抑制A549细胞增殖,呈剂量依赖性。彗星试验显示,DNA损伤随诺米林剂量的增加而增加。蛋白质免疫印迹分析表明,用诺米林预处理的A549细胞Bcl-2蛋白表达降低,Bax蛋白表达增加。高剂量(300mg/kg)、中剂量(200mg/kg)和低剂量(100mg/kg)诺米林处理的Lewis小鼠肺癌抑制率分别为43.70%、27.59%和20.14%(P<0.01)。随着诺米林的处理,Bax和Caspase-9蛋白表达增加,Bcl-2蛋白表达降低。
诺米林对肺癌细胞的体内外增殖均有一定的抑制作用。其机制可能与上调Bax和Caspase-9以及下调Bcl-2有关。