Department of Pathology, School of Pharmacy with the Division of Laboratory Medicine in Sosnowiec, Medical University of Silesia in Katowice, Ostrogórska 30, 41-200 Sosnowiec, Poland.
Department of Pharmaceutical Chemistry, School of Pharmacy with the Division of Laboratory Medicine in Sosnowiec, Medical University of Silesia in Katowice, Jagiellońska 4, 41-200 Sosnowiec, Poland.
Nutrients. 2017 Oct 19;9(10):1144. doi: 10.3390/nu9101144.
One of the deadliest cancers among women is a breast cancer. Research has shown that two natural substances occurring in propolis, caffeic acid (CA) and caffeic acid phenethyl ester (CAPE), have significant anticancer effects. The purpose of our in vitro study was to compare cytotoxic activity and migration rate inhibition using CA and CAPE (doses of 50 and 100 µm) against triple-negative, MDA-MB-231 breast adenocarcinoma line cells, drawn from Caucasian women. Viability was measured by XTT-NR-SRB assay (Tetrazolium hydroxide-Neutral Red-Sulforhodamine B) for 24 h and 48 h periods. Cell migration for wound healing assay was taken for 0 h, 8 h, 16 h, and 24 h periods. CAPE displayed more than two times higher cytotoxicity against MDA-MB-231 cells. IC values for the XTT assay were as follows: CA for 24 h and 48 h were 150.94 µM and 108.42 µM, respectively, while CAPE was 68.82 µM for 24 h and 55.79 µM for 48 h. For the NR assay: CA was 135.85 µM at 24 h and 103.23 µM at 48 h, while CAPE was 64.04 µM at 24 h and 53.25 µM at 48 h. For the SRB assay: CA at 24 h was 139.80 µM and at 48 h 103.98 µM, while CAPE was 66.86 µM at 24 h and 47.73 µM at 48 h. Both agents suspended the migration rate; however, CAPE displayed better activity. Notably, for the 100 µM CAPE dose, motility of the tested breast carcinoma cells was halted.
女性中最致命的癌症之一是乳腺癌。研究表明,蜂胶中存在两种天然物质,咖啡酸(CA)和咖啡酸苯乙酯(CAPE),具有显著的抗癌作用。我们的体外研究目的是比较使用 CA 和 CAPE(剂量为 50 和 100 µm)对源自高加索女性的三阴性、MDA-MB-231 乳腺腺癌系细胞的细胞毒性活性和迁移率抑制作用。通过 XTT-NR-SRB 测定法(四唑盐-中性红-磺基罗丹明 B)在 24 h 和 48 h 期间测量细胞活力。细胞迁移用于伤口愈合测定,时间为 0 h、8 h、16 h 和 24 h。CAPE 对 MDA-MB-231 细胞的细胞毒性作用高出两倍以上。XTT 测定的 IC 值如下:CA 在 24 h 和 48 h 时分别为 150.94 µM 和 108.42 µM,而 CAPE 在 24 h 时为 68.82 µM,在 48 h 时为 55.79 µM。对于 NR 测定:CA 在 24 h 时为 135.85 µM,在 48 h 时为 103.23 µM,而 CAPE 在 24 h 时为 64.04 µM,在 48 h 时为 53.25 µM。对于 SRB 测定:CA 在 24 h 时为 139.80 µM,在 48 h 时为 103.98 µM,而 CAPE 在 24 h 时为 66.86 µM,在 48 h 时为 47.73 µM。两种药物均暂停了迁移率;然而,CAPE 表现出更好的活性。值得注意的是,对于 100 µM CAPE 剂量,测试的乳腺癌细胞的运动性停止。