Resistance to irinotecan (CPT-11) activates epidermal growth factor receptor/nuclear factor kappa B and increases cellular metastasis and autophagy in LoVo colon cancer cells

Ming-Cheng CHEN, Nien-Hung LEE, Tsung-Jung HO, Hsi-Hsien HSU, Chia Hua KUO, Wei-Wen KUO, Yueh-Min LIN, Fuu-Jen TSAI, Chang-Hai TSAI, Chih-Yang HUANG

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32 Citations (Scopus)

Abstract

Chemotherapy is usually applied to treat colon cancer but leads to chemoresistance, and increased metastasis and invasion. The main focus of this study is to observe effects of resistance to irinotecan (CPT-11) on metastasis, invasion and autophagy in CPT-11 resistant (CPT-11-R) LoVo colon cancer cells. CPT-11, a topoisomerase I inhibitor and a first-line chemotherapeutic drug, is used to treat colon cancer. CPT-11-R cells were constructed in a step-wise fashion with increasing CPT-11 doses. The CPT-11-R strain had a significantly lower expression of Wnt/β-catenin pathway, but induced an EGFR/IKKα/β/NF-κB pathway with elevated cell cycle, metastasis and basal autophagy. Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Original languageEnglish
Pages (from-to)51-60
JournalCancer Letters
Volume349
Issue number1
Early online dateApr 2014
DOIs
Publication statusPublished - 2014

Citation

Chen, M.-C., Lee, N.-H., Ho, T.-J., Hsu, H.-H., Kuo, C.-H., Kuo, W.-W., Lin, Y.-M., Tsai, F.-J., Tsai, C.-H., & Huang, C. Y. (2014). Resistance to irinotecan (CPT-11) activates epidermal growth factor receptor/nuclear factor kappa B and increases cellular metastasis and autophagy in LoVo colon cancer cells. Cancer Letters, 349(1), 51-60. https://doi.org/10.1016/j.canlet.2014.03.023

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