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. 2016 Dec 15;7(12):e208. doi: 10.1038/ctg.2016.59

Table 2. Number of differentially methylated probes between tumors and normal tissues in several subgroups of CRC at a false discovery rate of 0.05 (q-value<0.05).

Data set HNPCC
Sporadic CRCa
CRCb
Subgroup Overall Lynch synd. FCCTX Overall MSI-L/MSS Overall
Samples 36/40 19/20 10/11 194/32 171/25 129/29
# Hypomethylation 240 307 200 922 1,060 321
 In CGI (%) 10 (4.2) 9 (2.9) 9 (4.5) 96 (10.4) 96 (9.1) 11 (3.4)
 In PR (%) 212 (89.5) 273 (89.5) 176 (88.9) 831 (91.5) 961 (91.8) 291 (91.5)
# Hypermethylation 590 780 170 1,497 1,387 1,182
 In CGI (%) 475 (80.5) 591 (75.8) 142 (83.5) 1,039 (69.4) 971 (70.0) 874 (73.9)
 In PR (%) 520 (97.6) 688 (96.5) 151 (97.4) 1,329 (96.4) 1,230 (96.5) 1,063 (97.3)

CGI, CpG island; CRC, colorectal cancer; FCCTX, familial colorectal cancer type X; HNPCC, hereditary nonpolyposis colorectal cancer; MSI, microsatellite instability; MSS, microsatellite stable; PR, promoter region; TCGA, the cancer genome atlas.

Row 3 gives the number of tumors and normal tissues in each data set, with that for tumors placed in the front; row 4 reports the number of hypomethylated probes; row 5 lists the number (percentage) of hypomethylated probes located in CGIs; row 6 describes the number (percentage) of hypomethylated probes located in PRs, which are defined as being located within 1 kb upstream and 1 kb downstream from the transcription start site; rows 7–9 provide information that is similar to that given in rows 4–6, but for hypermethylated probes.

a

TCGA.