| CPC C12Q 1/6886 (2013.01) [C12Q 1/6806 (2013.01); G16B 5/00 (2019.02); C12Q 2600/106 (2013.01); C12Q 2600/112 (2013.01); C12Q 2600/118 (2013.01); C12Q 2600/154 (2013.01)] | 6 Claims |
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1. A method for assessing bladder cancer risk in a human subject, comprising:
performing bisulfite treatment of a DNA of a urine sample obtained from said subject;
conducting methylation-specific quantitative PCR to amplify the DNA to obtain a CT value for at least one CpG region of the sequence of SEQ ID NO: 3, or the complementary sequence of SEQ ID NO: 3;
determining if bladder cancer is present in the subject based on comparing the obtained CT value of the at least one CpG region of the sample with a predetermined range of CT value of the at least one CpG regions, wherein the predetermined range of CT value was derived from a statistical analysis of a training set of samples including samples in which bladder cancer is present and samples in which bladder cancer is not present; and
treating the bladder cancer in the subject if it is determined that bladder cancer is present in the subject.
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