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Caffeic acid phenethyl ester suppresses proliferation and survival of TW2.6 human oral cancer cells via inhibition of akt signaling
Journal article   Open access   Peer reviewed

Caffeic acid phenethyl ester suppresses proliferation and survival of TW2.6 human oral cancer cells via inhibition of akt signaling

Ying-Yu Kuo, Hui-Ping Lin, Chieh Huo, Liang-Cheng Su, Jonathan Yang, Ping-Hsuan Hsiao, Hung-Che Chiang, Chi-Jung Chung, Horng-Dar Wang, Jang-Yang Chang, …
International Journal of Molecular Sciences, Vol.14(5), pp.8801-8817
2013

Abstract

5-fluorouracil Akt Akt1 Akt2 Caffeic acid phenethyl ester Cell cycle Cell proliferation Cyclin D1 FOXO1 FOXO3a NF- B Oral cancer P27 Phospho-Akt Ser473 Phospho-Akt Thr 308 Phospho-FOXO1 Thr24 Phospho-FoxO3a Thr32 Phospho-NF- B Ser536 Phospho-Rb Ser807/811 Rb Skp2 TW2.6
Caffeic acid phenethyl ester (CAPE) is a bioactive component extracted from honeybee hive propolis. Our observations indicated that CAPE treatment suppressed cell proliferation and colony formation of TW2.6 human oral squamous cell carcinoma (OSCC) cells dose-dependently. CAPE treatment decreased G1 phase cell population, increased G2/M phase cell population, and induced apoptosis in TW2.6 cells. Treatment with CAPE decreased protein abundance of Akt, Akt1, Akt2, Akt3, phospho-Akt Ser473, phospho-Akt Thr 308, GSK3β, FOXO1, FOXO3a, phospho-FOXO1 Thr24, phospho-FoxO3a Thr32, NF-κB, phospho-NF-κB Ser536, Rb, phospho-Rb Ser807/811, Skp2, and cyclin D1, but increased cell cycle inhibitor p27Kip. Overexpression of Akt1 or Akt2 in TW2.6 cells rescued growth inhibition caused by CAPE treatment. Co-treating TW2.6 cells with CAPE and 5-fluorouracil, a commonly used chemotherapeutic drug for oral cancers, exhibited additive cell proliferation inhibition. Our study suggested that administration of CAPE is a potential adjuvant therapy for patients with OSCC oral cancer. © 2013 by the authors; licensee MDPI, Basel, Switzerland.
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https://doi.org/10.3390/ijms14058801View
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