Migration Rate Inhibition of Breast Cancer Cells Treated by Caffeic Acid and Caffeic Acid Phenethyl Ester: An In Vitro Comparison Study

被引:74
|
作者
Kabala-Dzik, Agata [1 ]
Rzepecka-Stojko, Anna [2 ]
Kubina, Robert [1 ]
Jastrzebska-Stojko, Zaneta [3 ]
Stojko, Rafal [4 ]
Wojtyczka, Robert Dariusz [5 ]
Stojko, Jerzy [6 ]
机构
[1] Med Univ Silesia, Div Lab Med Sosnowiec, Sch Pharm, Dept Pathol, Ostrogorska 30, PL-41200 Sosnowiec, Poland
[2] Med Univ Silesia, Div Lab Med Sosnowiec, Sch Pharm, Dept Pharmaceut Chem, Jagiellonska 4, PL-41200 Sosnowiec, Poland
[3] Med Univ Silesia, Prof K Gibinski Univ Clin Ctr, Dept Anesthesiol & Intens Care, Ceglana 35, PL-40514 Katowice, Poland
[4] Med Univ Silesia, Sch Hlth Sci, Dept Women Hlth, Medykow 12, PL-40752 Katowice, Poland
[5] Med Univ Silesia, Div Lab Med Sosnowiec, Sch Pharm, Dept & Inst Microbiol & Virol, Jagiellonska 4, PL-41200 Sosnowiec, Poland
[6] Med Univ Silesia, Div Lab Med Sosnowiec, Sch Pharm, Dept Toxicol & Bioanal, Jagiellonska 4, PL-41200 Sosnowiec, Poland
关键词
caffeic acid; CAPE; migration; wound healing; breast cancer; propolis; NF-KAPPA-B; ESTROGEN-RECEPTOR; PROPOLIS EXTRACT; CARCINOMA CELLS; ETHANOL EXTRACT; GROWTH ARREST; MEDICINE USE; APOPTOSIS; CAPE; COMPLEMENTARY;
D O I
10.3390/nu9101144
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
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 mu m) 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. IC50 values for the XTT assay were as follows: CA for 24 h and 48 h were 150.94 mu M and 108.42 mu M, respectively, while CAPE was 68.82 mu M for 24 h and 55.79 mu M for 48 h. For the NR assay: CA was 135.85 mu M at 24 h and 103.23 mu M at 48 h, while CAPE was 64.04 mu M at 24 h and 53.25 mu M at 48 h. For the SRB assay: CA at 24 h was 139.80 mu M and at 48 h 103.98 mu M, while CAPE was 66.86 mu M at 24 h and 47.73 mu M at 48 h. Both agents suspended the migration rate; however, CAPE displayed better activity. Notably, for the 100 mu M CAPE dose, motility of the tested breast carcinoma cells was halted.
引用
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页数:19
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