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. 2018 Dec 19;13(12):e0208026. doi: 10.1371/journal.pone.0208026

Table 5. Differences in gene expression between M and NM MCTs measured by RT-qPCR.

  RT-qPCR  
Gene symbol/ID. Exon-level fold changea (NM/M) No. NM MCTsb No. M MCTsb Fold changec (NM/M) Spearman RCCd p-valuee (Array)
CD9 2.25 (1.80) 12 8 2.78 0.51 0.405 (0.090)
DSP 19.08 (1.48) 7 4 40.43 0.74 0.217 (0.152)
EGR1 3.66 (2.11) 11 14 6.05 0.69 0.028 (0.050)
ENSCAFG-30560 2.05 (1.43) 5 8 7.15 0.81 0.139 (0.213)
KRT10 23.43 (43.37) 11 12 53.87 0.88 0.009 (0.017)
KRTAP4-4 2.10 (2.77) 7 7 1.12 0.76 0.730 (0.208)
PERP 7.38 (4.69) 11 10 9.94 0.80 0.083 (0.041)
SBSN 3.49 (2.62) 10 6 14.77 0.81 0.140 (0.115)
SNORD93 0.25 (0.39) 12 16 0.37 0.50 0.196 (0.258)

aFold change differences in expression between 18 M and 16 NM MCTs determined by microarray—Ratio of median expression values for the Exon probe set upon which RT-qPCR assay design was based. In parenthesis are the fold change differences calculated when only the microarray-derived expression values of MCTs that yielded valid Cq values in RT-qPCR assay were considered.

bThe numbers of NM and M MCTs represent the numbers of samples for which valid Cq (Cq <35; Cq SD<0.5) measurements were obtained. ‘Non-valid’ Cq values were attributable to: Cq <35 or ‘undetermined’ and Cq SD>0.5.

cFold change determined by RT-qPCR assay.

dThe Spearman rank correlation coefficient (RCC) indicates the extent of the concordance between the expression values for individual MCT assayed by microarray and RT-qPCR, respectively.

eThe statistical significance of the RT-qPCR measured differences in expression between the NM and M MCTs determined by t-test. The statistical significance of the differences between the microarray-derived gene-level expression values measured for the same MCTs is shown in parenthesis.