Curcumin Analogue CA15 Exhibits Anticancer Effects on HEp-2 Cells via Targeting NF-κB
Author(s) -
Jian Chen,
Linlin Zhang,
Yilai Shu,
Chen Li-ping,
Min Zhu,
Song Yao,
Jiabing Wang,
Jianzhang Wu,
Guang Liang,
Haitao Wu,
Wulan Li
Publication year - 2017
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2017/4751260
Subject(s) - curcumin , apoptosis , flow cytometry , mtt assay , western blot , cancer research , viability assay , chemistry , in vitro , cancer cell , pharmacology , nf κb , cell culture , cancer , cell growth , microbiology and biotechnology , medicine , biology , biochemistry , genetics , gene
Laryngeal carcinoma remains one of the most common malignancies, and curcumin has been proven to be effective against head and neck cancers in vitro. However, it has not yet been applied in clinical settings due to its low stability. In the current study, we synthesized 34 monocarbonyl analogues of curcumin with stable structures. CA15, which exhibited a stronger inhibited effect on laryngeal cancer cells HEp-2 but a lower toxicity on hepatic cells HL-7702 in MTT assay, was selected for further analysis. The effects of CA15 on cell viability, proliferation, migration, apoptosis, and NF- κ B activation were measured using MTT, Transwell migration, flow cytometry, Western blot, and immunofluorescence assays in HEp-2 cells. An NF- κ B inhibitor, BMS-345541, as well as curcumin was also tested. Results showed that CA15 induced decreased toxicity towards HL-7702 cells compared to curcumin and BMS-345541. However, similar to BMS-345541 and curcumin, CA15 not only significantly inhibited proliferation and migration and induced caspase-3-dependent apoptosis but also attenuated TNF- α -induced NF- κ B activation in HEp-2 cells. These results demonstrated that curcumin analogue CA15 exhibited anticancer effects on laryngeal cancer cells via targeting of NF- κ B.
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