Table 1. Relative expression analysis of genes associated with NER.
Gene Symbol | Definition | Fold change | p value |
TP53 | Tumor protein p53 | 1.83 | 0.017* |
CDKN1A | Cyclin-dependent kinase inhibitor 1A | 2.3 | 0.003* |
RPA32 | Replication Protein A | 0.85 | 0.31 |
H2AX | H2A histone family, member X | 1.21 | 0.17 |
PCNA | Proliferating Cell Nuclear Antigen | 0.34 | 0.006* |
POLH | Polymerase (DNA directed), eta | 0.45 | 0.004* |
DDB1 | Damage-specific DNA Binding Protein 1 | 0.091 | 0.0001* |
DDB2 | Damage-specific DNA Binding Protein 2 | 0.62 | 0.0527 |
ERCC8 | Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 8 (CSA) | 0.73 | 0.061 |
ERCC6 | Excision Repair Cross-complementing rodent repair deficiency, Complementation group 6 (CSB) | 0.42 | 0.015* |
XPA | Xeroderma Pigmentosum, complementation group A | 0.82 | 0.077 |
ERCC5 | Excision Repair Cross-complementing rodent repair deficiency, Complementation group 5 (XPG) | 0.83 | 0.098 |
Expression analysis of NER, cell cycle regulation and DNA damage detection factors in LB1 silenced and control cells. mRNA from Sc and shLB1 U-2 OS cells was prepared at 3 days after silencing and analyzed by qRT-PCR using GAPDH as a reference gene. The change in expression of a specific gene was considered significant if the “fold change” was higher than 1.7 or lower than 0.6.