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. 2014 Jul 21;20(27):8928–8938. doi: 10.3748/wjg.v20.i27.8928

Figure 1.

Figure 1

Outline of quantitative methylation-specific polymerase chain reaction analysis in peritoneal lavage. The depth of invasion and subsequent increased likelihood of tumor cells exfoliated from colonic serosa is reflected in the presence of tumor-related methylated DNA in peritoneal cavity. In quantitative methylation-specific polymerase chain reaction (PCR) step, the DNA polymerase cleaves only probes that are hybridized to the target. Cleavage separates the reporter dye (R) from the quencher dye (Q); resulting in increased fluorescence by the reporter. The increase in fluorescence signal occurs only if the target sequence is complementary to the probe and is amplified during PCR.