首页> 美国卫生研究院文献>Molecules >Comparison of Two Components of Propolis: Caffeic Acid (CA) and Caffeic Acid Phenethyl Ester (CAPE) Induce Apoptosis and Cell Cycle Arrest of Breast Cancer Cells MDA-MB-231
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Comparison of Two Components of Propolis: Caffeic Acid (CA) and Caffeic Acid Phenethyl Ester (CAPE) Induce Apoptosis and Cell Cycle Arrest of Breast Cancer Cells MDA-MB-231

机译:蜂胶两种成分的比较:咖啡酸(CA)和咖啡酸苯乙基酯(CAPE)诱导乳腺癌细胞MDA-MB-231凋亡和细胞周期阻滞。

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摘要

Studies show that caffeic acid (CA) and caffeic acid phenethyl ester (CAPE) are compounds with potent chemopreventive effects. Breast cancer is a common form of aggressive cancer among women worldwide. This study shows a comparison of CA and CAPE activity on triple-negative human caucasian breast adenocarcinoma line cells (MDA-MB-231). MDA-MB-231 cells were treated by CA and CAPE with doses of from 10 to 100 µM, for periods of 24 h and 48 h. Cytotoxicity MTT tests, apoptosis by Annexin V, and cell cycle with Dead Cell Assays were performed. Cytotoxic activity was greater for CAPE compared to CA (both incubation times, same dosage). IC50 values for CAPE were 27.84 µM (24 h) and 15.83 µM (48 h) and for CA > 10,000 µM (24 h) and > 1000 µM (48 h). Polyphenols induced apoptosis, while CAPE (dose dependently), induced a higher apoptotic effect. CAPE also induced cell cycle arrest in S phase (time and dose dependently), CA did it only for 50 and 100 µM. A dose dependent decline was seen for the G0/G1 phase (CAPE, 48 h), as well as elimination of phase G2/M by 100 µM of CAPE (only mild effect for CA). Comparing CA and CAPE activity on MDA-MB-231, CAPE clearly showed better activity for the same dosages and experiment times.
机译:研究表明,咖啡酸(CA)和咖啡酸苯乙酯(CAPE)是具有有效化学预防作用的化合物。乳腺癌是全世界女性中侵袭性癌症的一种常见形式。这项研究显示了CA和CAPE对三阴性人类白种人乳腺腺癌细胞系(MDA-MB-231)的活性的比较。用CA和CAPE以10至100 µM的剂量处理MDA-MB-231细胞24小时和48小时。进行了细胞毒性MTT测试,膜联蛋白V的凋亡以及死细胞测定的细胞周期。与CA相比,CAPE的细胞毒活性更高(均孵育时间,相同剂量)。 CAPE的IC50值为27.84 µM(24小时)和15.83 µM(48小时),CA> 10,000 µM(24小时)和> 1000 µM(48小时)。多酚诱导凋亡,而CAPE(取决于剂量)诱导更高的凋亡作用。 CAPE还诱导了S期的细胞周期停滞(时间和剂量依赖性),CA仅在50和100 µM时才起作用。对于G0 / G1期(CAPE,48小时),剂量依赖性下降,并且100 µM的CAPE消除了G2 / M期(对CA仅有轻微的影响)。比较CA和CAPE在MDA-MB-231上的活性,在相同的剂量和实验时间下,CAPE显然显示出更好的活性。

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