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. 2017 Mar 14;5:e3084. doi: 10.7717/peerj.3084

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© 2017 Zhu et al.

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.

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(A) The mRNA expression of DAPK was detected using real-time PCR. S1–S15, patient codes. The cDNA from HEK293T cells were used as a positive control and formation of the standard curve. (B) Correlation analysis of DAPK mRNA expression and DAPK promoter methylation rate in breast cancer samples. (C) Correlation analysis of the T/N ratio of DAPK mRNA expression and DAPK promoter methylation rate in breast cancer samples.