Oligo-microarray analysis reveals the role of cyclophilin A in drug resistance
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Abstract
Cyclophilin A (CYPA) belongs to peptidyl prolyl isomerases (PPIases), which catalyze the cis/trans isomerization of prolyl peptide bonds in cellular communication. CYPA has been implicated in several pathological processes, including cancer, inflammatory diseases, and HIV-1 infection. Up-regulation of CYPA has been found to be a common phenomenon in several tumor types, including in hepatocellular carcinoma (HCC). However, the role of CYPA in tumor cells remains unknown. We generated a stable SK-Hep1 cell line and studied the CYPA regulated genes at the transcriptome level. The microarray results reveal that CYPA can up-regulate the expression of many cytokine and drug resistance related genes. Furthermore, we showed that the elevated CYPA expression contributes to drug resistance. We postulate that the over-expression of CYPA in tumors may play a role in clinical resistance to chemotherapy.
Keywords
Oligo-microarray Peptidyl–prolyl isomerase (PPIase) Cyclophilin A (CYPA/PPIA) Hepatocellular carcinoma (HCC) Multi-drug resistant protien (MRP)Notes
Acknowledgments
This work was supported by the Graduate Innovation Foundation of Fudan University (No. EYH1322021).
Supplementary material
References
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