The flavonoid p-hydroxycinnamic acid exhibits anticancer effects in human pancreatic cancer MIA PaCa-2 cells in vitro: Comparison with gemcitabine

• Type of Material: Article
• Authors: Masayoshi Yamaguchi, Emory University; Tomiyasu Murata, Meijo University; Bassel El-Rayes, Emory University; Mamoru Shoji, Emory University
• Language: English
• Date: 2015-09-17
• Publisher: Spandidos Publications
• Publication Version: Final Published Version
• Copyright Statement: © Spandidos Publications 2015
• Final Published Version (URL): http://dx.doi.org/10.3892/or.2015.4282
• Title of Journal or Parent Work: Oncology Reports
• ISSN: 1021-335X
• Volume: 34
• Issue: 6
• Keywords: apoptotic cell death; MIA PaCa-2 cells; cell proliferation; pancreatic cancer; p-hydroxycinnamic acid; Pt45P1 cells

Abstract

Pancreatic cancer is a highly aggressive malignancy with a notoriously dismal prognosis. A major contributor to this poor clinical outcome is pancreatic cancer's prominent chemoresistance. The present study was undertaken to determine whether the flavonoid p‑hydroxycinnamic acid (HCA), which is a botanical factor, possesses anticancer effects on cloned human pancreatic cancer MIA PaCa‑2 cells that possess resistance to radiation therapy in vitro. Proliferation of MIA PaCa‑2 cells was suppressed after culture with HCA (10‑1,000 nM). Such an effect was also noted in human pancreatic cancer Pt45P1 cells. In the MIA PaCa‑2 cells, HCA induced G1 and G2/M phase cell cycle arrest in the cells. The suppressive effects of HCA on proliferation were suggested to be mediated through the inhibition of various signaling pathways related to nuclear factor‑κB (NF‑κB), extracellular signal‑regulated kinase (ERK), protein kinase C, phosphatidylinositol 3‑kinase (PI3K) or nuclear transcription activity. Moreover, HCA was found to stimulate cell death in the MIA PaCa‑2 and Pt45P1 cells in vitro. The anticancer effects of HCA on MIA PaCa‑2 cells were exhibited at a lower concentration than gemcitabine, a potent cancer drug. The flavonoid HCA may be a useful tool in the therapy of human pancreatic cancer in vivo.