Afaq Farrukh, Zaman Najia, Khan Naghma, Syed Deeba N, Sarfaraz Sami, Zaid Mohammad Abu, Mukhtar Hasan
Department of Dermatology, University of Wisconsin, Madison, WI 53706, USA.
Int J Cancer. 2008 Oct 1;123(7):1508-15. doi: 10.1002/ijc.23675.
Inhibitors of the epidermal growth factor receptor (EGFR) have generated considerable hope for cancer treatment, specifically for lung and breast cancers. Therefore, identification of a natural, nontoxic agent(s) as an inhibitor of EGFR is of considerable importance. Delphinidin, an anthocyanidin present in pigmented fruits and vegetables, possesses potent antioxidant and antiproliferative properties. In our study, employing EGFR positive breast cancer AU-565 cells and immortalized MCF-10A cells, we evaluated the effect of delphinidin on EGFR and its downstream signaling pathways. Delphinidin (5-40 microM; 3 hr) treatment of both AU-565 cells and MCF-10A cells inhibited the (i) phosphorylation of EGFR, (ii) activation of PI3K, (iii) phosphorylation of AKT and MAPK. Further, delphinidin treatment of AU-565 cells inhibited EGF-induced autophosphorylation of EGFR, AKT and MAPK, activation of PI3K and cell invasion. We then compared the growth inhibitory effects of delphinidin (5-40 microM; 48 hr), and found that it resulted in a decrease in cell growth of AU-565 and MCF-10A cells but had only minimal effects on normal mammary epithelial 184A1 cells. Treatment of AU-565 cells with delphinidin resulted in (i) induction of apoptosis, (ii) cleavage of PARP protein, (iii) activation of caspase-3 and (iv) downregulation of Bcl-2 with an increase in the expression of Bax. In summary, our study identifies a naturally occurring dietary agent delphinidin as an effective inhibitor of EGFR signaling in breast cancer cells. We suggest that delphinidin could be developed as an agent for the management of EGFR positive human cancers.
表皮生长因子受体(EGFR)抑制剂为癌症治疗,尤其是肺癌和乳腺癌的治疗带来了巨大希望。因此,鉴定一种天然、无毒的EGFR抑制剂具有相当重要的意义。飞燕草色素是一种存在于有色水果和蔬菜中的花青素,具有强大的抗氧化和抗增殖特性。在我们的研究中,我们使用EGFR阳性的乳腺癌AU-565细胞和永生化的MCF-10A细胞,评估了飞燕草色素对EGFR及其下游信号通路的影响。用飞燕草色素(5 - 40微摩尔;3小时)处理AU-565细胞和MCF-10A细胞,抑制了(i)EGFR的磷酸化,(ii)PI3K的激活,(iii)AKT和MAPK的磷酸化。此外,用飞燕草色素处理AU-565细胞抑制了EGF诱导的EGFR、AKT和MAPK的自磷酸化、PI3K的激活以及细胞侵袭。然后我们比较了飞燕草色素(5 - 40微摩尔;48小时)的生长抑制作用,发现它导致AU-565和MCF-10A细胞的生长减少,但对正常乳腺上皮184A1细胞只有极小的影响。用飞燕草色素处理AU-565细胞导致(i)细胞凋亡的诱导,(ii)PARP蛋白的切割,(iii)caspase-3的激活,以及(iv)Bcl-2的下调和Bax表达的增加。总之,我们的研究确定了一种天然存在的膳食成分飞燕草色素是乳腺癌细胞中EGFR信号的有效抑制剂。我们建议飞燕草色素可以开发成为一种用于治疗EGFR阳性人类癌症的药物。