Upregulation of ID2 antagonizes arsenic trioxide-induced antitumor effects in cancer cells
Aims and background. Arsenic trioxide (ATO) strongly induces apoptosis and differentiation in acute promyelocytic leukemia, and induces cell cycle arrest in most solid tumors. Although many signaling pathways are involved in its antitumor mechanism, a detailed investigation of the transforming growth factor beta-bone morphogenetic protein signaling pathway has not been performed. Methods and study design. A microarray containing 113 genes associated with the pathway was used to screen important molecules that participate in the antitumor effects of ATO. The expression levels of the inhibitors of DNA binding-2 (ID2) in 4 different types of cancer cells were determined by quantitative reverse transcription PCR and Western blotting. Human esophageal squamous cell carcinoma cell line Eca109 and pancreatic carcinoma cell line BxPC3 cells were transfected with siRNAs targeting ID2 and scrambled control siRNA. Cell proliferation was evaluated by methyl thiazolyl tetrazolium assay. Results. Eighteen upregulated and 12 downregulated genes were identified. After verification at the transcriptional and translational levels in 4 different cancer cells, ID2 was identified as an ATO antitumor-associated protein. In addition, specific silencing of ID2 could enhance ATO-induced cell proliferation inhibition in cancer cells. Conclusions. A combination of ATO and ID2-targeted agents may have considerable therapeutic benefits in cancers.
Tumori 2014; 100(3): 352 - 357
Article Type: ORIGINAL RESEARCH ARTICLE
Xueyan Zhang, Chengqian Lv, Bing Du, Xiao Ma, Jingming Guan, Shanling Gao, Xiaodong Li, Lei Zheng, Guang-Hua Lei
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