Kabała-Dzik Agata, Rzepecka-Stojko Anna, Kubina Robert, Wojtyczka Robert Dariusz, Buszman Ewa, Stojko Jerzy
1 Medical University of Silesia in Katowice, School of Pharmacy with the Division of Laboratory Medicine in Sosnowiec, Poland.
Integr Cancer Ther. 2018 Dec;17(4):1247-1259. doi: 10.1177/1534735418801521. Epub 2018 Sep 24.
Epithelium mammary carcinoma is a cancer with a high death rate among women. One factor having a significant impact on metastasis is cell migration. The aim of this study was to compare migration rate inhibition of caffeic acid (CA) and its phenethyl ester (CAPE) on MCF-7 breast cancer cells. Microscopic evaluation was used to determine the morphology of carcinoma cells, before and after 24-hour treatment with CA and CAPE using a dose of 50 µM. The cytotoxic effect was measured by XTT-NR-SRB assay (tetrazolium hydroxide-neutral red-Sulforhodamine B) for 24-hour and 48-hour periods, using CA and CAPE, with doses of 50 and 100 µM. These doses were used to determine cell migration inhibition using a wound closure assay for 0-hour, 8-hour, 16-hour, and 24-hour periods. Both CA and CAPE treatments displayed cytotoxic activity in a dose- and time-dependent trend. CAPE displayed IC values more than twice as low as CA. IC values for the XTT assay were as follows: CA was 102.98 µM for 24 hours and 59.12 µM for 48 hours, while CAPE was 56.39 µM for 24 hours and 28.10 µM for 48 hours. For the NR assay: CA was 84.87 µM at 24 hours and 65.05 µM at 48 hours, while CAPE was 69.05 µM at 24 hours and 29.05 µM at 48 hours. For the SRB assay: At 24 hours, CA was 83.47 µM and 53.46 µM at 48 hours, while CAPE was 38.53 µM at 24 hours and 20.15 µM at 48 hours. Both polyphenols induced migration inhibition, resulting in practically halting the wound closure. CAPE produced better results than CA with the same doses and experiment times, though both CA and CAPE displayed cytotoxic activity against MCF-7 cells, as well as inhibited migration.
乳腺上皮癌是一种在女性中死亡率很高的癌症。对转移有重大影响的一个因素是细胞迁移。本研究的目的是比较咖啡酸(CA)及其苯乙酯(CAPE)对MCF-7乳腺癌细胞迁移率的抑制作用。使用显微镜评估来确定癌细胞在用50 µM剂量的CA和CAPE处理24小时前后的形态。使用XTT-NR-SRB测定法(氢氧化四唑-中性红-磺酰罗丹明B)在24小时和48小时期间测量细胞毒性作用,使用剂量为50和100 µM的CA和CAPE。这些剂量用于在0小时、8小时、16小时和24小时期间使用伤口愈合试验确定细胞迁移抑制。CA和CAPE处理均呈现出剂量和时间依赖性的细胞毒性活性。CAPE的半数抑制浓度(IC)值比CA低两倍多。XTT测定法的IC值如下:CA在24小时时为102.98 µM,在48小时时为59.12 µM,而CAPE在24小时时为56.39 µM,在48小时时为28.10 µM。对于中性红(NR)测定法:CA在24小时时为84.87 µM,在48小时时为65.05 µM,而CAPE在24小时时为69.05 µM,在48小时时为29.05 µM。对于磺酰罗丹明B(SRB)测定法:在24小时时,CA为83.47 µM,在48小时时为53.46 µM,而CAPE在24小时时为38.53 µM,在48小时时为20.15 µM。两种多酚均诱导迁移抑制,导致伤口愈合几乎停止。在相同剂量和实验时间下,CAPE比CA产生了更好的结果,尽管CA和CAPE均对MCF-7细胞显示出细胞毒性活性,并抑制了迁移。