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. 2017 Dec 18;15(3):3287–3294. doi: 10.3892/ol.2017.7633

Table I.

Primers used in the present study.

Primer name Primer sequence (5′-3′)
DACT2 qPCR
  Forward CGGTCGGTTGATGAGACTACT
  Reverse CAGGGCTCTGTCAAGATCACC
CyclinD1 qPCR
  Forward GCTGCGAAGTGGAAACCATC
  Reverse CCTCCTTCTGCACACATTTGAA
MMP7 qPCR
  Forward GAGTGAGCTACAGTGGGAACA
  Reverse CTATGACGCGGGAGTTTAACAT
GAPDH qPCR
  Forward ATGGGGAAGGTGAAGGTCG
  Reverse GGGGTCATTGATGGCAACAATA
DACT2 ORF
  Forward CGGGATCCGCCGCTCGTGGGGTTCGGGA
  Reverse CGACGCGTACCATGGTCATGACCTTCA
β-catenin reporter (wide)
  Forward CGCGTAACTGACAGATCAAAGGGGGTAAGATCAAAGGGGGTAGTCAACTC
  Reverse TCGAGAGTTGACTACCCCCTTTGATCTTACCCCCTTTGATCTGTCAGTTA
β-catenin reporter (mutant)
  Forward CGCGTAACTGACAGATCCCCTTTTTTAAGATCCCCTTTTTTAGTCAACTC
  Reverse TCGAGAGTTGACTAAAAAAGGGGATCTTAAAAAAGGGGATCTGTCAGTTA
MSP primers
  Methylated forward GCGCGTGTAGATTTCGTTTTTCGC
  Methylated reverse AACCCCACGAACGACGCCG
  Unmethylated forward TTGGGGTGTGTGTAGATTTTGTTTTTTGT
  Unmethylated reverse CCCAAACCCCACAAACAACACCA

qPCR, quantitative polymerase chain reaction; DACT2, dishevelled-associated antagonist of β-catenin homolog 2; MMP7, matrix metalloprotease 7; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; MSP, methylation-specific polymerase chain reaction.