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. 2011 Feb 7;6(2):e14661. doi: 10.1371/journal.pone.0014661

Table 3. Silencing of PKCδ prevents the genotoxic effects triggered by etoposide and BSO in SH-SY-5Y and in SK-N-BE-2C cells, respectively.

SH-SY-5Y SK-N-BE-2C
standard (A.U.) fpg (A.U.) Standard (A.U.) fpg (A.U.)
CTR NoT 0.0006±0.0001 0.0004±0.0001 0.0008±0.0001 0.0006±0.0001
siPKCδ 0.0006±0.0001 0.0007±0.0001 0.0009±0.0001 0.0008±0.0001
ETOPO NoT 0.0004±0.0001 8.352±2.8754**,§§ - -
siPKCδ 0.0006±0.0001 0.0004±0.0001## - -
BSO NoT - - 11.325±2.184♦♦ 13.215±1.969**
siPKCδ - - 0.0007±0.0001§§ 0.0006±0.0001##

NB cells, silenced for PKCδ, were treated with 0.07 µM etoposide (SH-SY-5Y) and 1 mM BSO (SK-N-BE-2C) for 24 h. DNA fragmentation (standard) and oxidation (fpg) were evaluated by comet test. The reported values derive from tail moment analyses.

**p<0.01 vs NoT CTR fpg;

♦♦

p<0.01 vs NoT CTR standard;

§§

p<0.01 vs NoT + ETOPO/BSO standard,

##

p<0.01 vs NoT ETOPO/BSO fpg.