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. 2021 Jun 17;13(12):15833–15874. doi: 10.18632/aging.203203

Table 1. A comparison between analyzed parameters in cells lacking active DNMT2/TRDMT1 gene (D-NIC cells) and in cells with functional DNMT2/TRDMT1 gene (C-NIC cells) during doxorubicin- or etoposide-induced senescence (35 nM DOX or 1 μM ETOPO).

Parameter C-NIC cells versus D-NIC cells
HeLa MDA-MB-231 U-2 OS U-251 MG
DOX ETOPO DOX ETOPO DOX ETOPO DOX ETOPO
cell cycle - G0/G1↑ G2/M↑ G2/M↑ - - G2/M↑ G2/M↑
SA-β-gal activity - - - - - -
p21 - - - -
apoptosis - -
senolytic activity of 1 μM AZA
(apoptosis)

(apoptosis)
- - -
(necrosis)
- -
ROS - -
DNA damage - - - -
micronuclei - - - - -
pATM(+)pH2AX(+) - -
53BP1 - - -
RNA-DNA hybrids - - - - - -
RAD51 - - - - -
RAD52 - - - - -
XRCC1 - -
LC3 - - - -
p62 - - - -
lysosomes - - -
NF-κB - - - - - -
IL-1β - - - - -
IL-6 - - - - - - -
IL-8 - - - - -
NSUN1 - - - - -
NSUN2 - - -
NSUN3 - - - - -
NSUN4 - - - - - - -
NSUN5 - - - - - - -
NSUN6 - - - - - -
cytoplasmic 5-mC - - -
nuclear 5-mC - - - - -

Four different cancer cellular models were considered, namely HeLa, MDA-MB-231, U-2 OS and U-251 MG cells. ↑ (red), statistically significant increase in analyzed parameter compared to corresponding C-NIC cells; ↓ (green), statistically significant decrease in analyzed parameter compared to corresponding C-NIC cells; - (gray), no statistically significant changes compared to corresponding C-NIC cells.