Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/5903
Title: Anti-proliferative, apoptotic and signal transduction effects of hesperidin in non-small cell lung cancer cells
Authors: Çinçin, Zeynep Birsu
Ünlü, Miray
Kıran, Bayram
Bireller, Elif Sinem
Baran, Yusuf
Çakmakoğlu, Bedia
Ünlü, Miray
Baran, Yusuf
Keywords: Anti-proliferative effect
Apoptosis
Gene expression profile
Hesperidin
Non-small cell lung cancer
Issue Date: 29-Jun-2015
Publisher: Springer Verlag
Source: Çinçin, Z. B., Ünlü, M., Kıran, B., Bireller, E. S., Baran, Y., and Çakmakoğlu, B. (2015). Anti-proliferative, apoptotic and signal transduction effects of hesperidin in non-small cell lung cancer cells. Cellular Oncology, 38(3), 195-204. doi:10.1007/s13402-015-0222-z
Abstract: Purpose: Hesperidin, a glycoside flavonoid, is thought to act as an anti-cancer agent, since it has been found to exhibit both pro-apoptotic and anti-proliferative effects in several cancer cell types. The mechanisms underlying hesperidin-induced growth arrest and apoptosis are, however, not well understood. Here, we aimed to investigate the anti-proliferative and apoptotic effects of hesperidin on non-small cell lung cancer (NSCLC) cells and to investigate the mechanisms involved. Methods: The anti-proliferative and apoptotic effects of hesperidin on two NSCLC-derived cell lines, A549 and NCI-H358, were determined using a WST-1 colorimetric assay, a LDH cytotoxicity assay, a Cell Death Detection assay, an AnnexinV-FITC assay, a caspase-3 assay and a JC-1 assay, respectively, all in a time- and dose-dependent manner. As a control, non-cancerous MRC-5 lung fibroblasts were included. Changes in whole genome gene expression profiles were assessed using an Illumina Human HT-12v4 beadchip microarray platform, and subsequent data analyses were performed using an Illumina Genome Studio and Ingenuity Pathway Analyser (IPA). Results: We found that after hesperidin treatment, A549 and NCI-H358 cells exhibited decreasing cell proliferation and increasing caspase-3 and other apoptosis-related activities, in conjunction with decreasing mitochondrial membrane potential activities, in a dose- and time-dependent manner. Through a GO analysis, by which changes in gene expression profiles were compared, we found that the FGF and NF-κB signal transduction pathways were most significantly affected in the hesperidin treated NCI-H358 and A549 NSCLC cells. Conclusions: Our results indicate that hesperidin elicits an in vitro growth inhibitory effect on NSCLC cells by modulating immune response-related pathways that affect apoptosis. When confirmed in vivo, hesperidin may serve as a novel anti-proliferative agent for non-small cell lung cancer.
URI: https://doi.org/10.1007/s13402-015-0222-z
http://hdl.handle.net/11147/5903
ISSN: 2211-3428
Appears in Collections:Molecular Biology and Genetics / Moleküler Biyoloji ve Genetik
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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