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. 2020 Jun 23;10:10149. doi: 10.1038/s41598-020-66797-x

Table 1.

Mutation status of crucial genes and the total number of differentially methylated (DM) CpGs with Δβ value ≥0.2 or ≤−0.2 in KRAS-depleted pancreatic cancer cell lines.

Cell Line KRAS CDKN2A TP53 SMAD4 Hypermethylated Promoter CpGs/total CpGs Hypomethylated Promoter CpGs/total CpGs All CpGs with Δβ
≥0.2 or ≤−0.2
Pa16C G12D/WT I255N* 434/3275 764/5613 8888
Pa01C G12D/WT T155P* Del* 175/1248 393/2998 4246
PANC-1 G12D/WT Del* R273H* 128/717 556/3136 3853
Panc 10.05 G12D/WT I255N/WT 59/452 275/1508 1960
Pa04C G12V* Del* Del* 13/172 25/200 372
Pa02C Q61H* Del* L247P* Del* 28/185 28/184 369
CFPAC-1 G12V/WT C242R* Del* 7/89 12/115 204
HPAC G12D* Stop/Stop 16/104 15/92 196
HPAF-II G12D/WT Del-FS* P151S* 14/96 5/68 164
SW-1990 G12D* Del* 11/78 15/79 157
Pa18C G12D/WT Del* Del* 6/72 6/72 144

The CpG methylation in Pa16C, Pa01C, PANC-1 and Panc 10.05 cells appears to be the most responsive to KRAS depletion. Homozygous mutations are represented with an asterisk.