A composition for non-invasive screening of early lung cancer and its application
A composition and technology for lung cancer, which are applied in biochemical equipment and methods, determination/inspection of microorganisms, etc., can solve the problem of less circulating DNA in tumors, and achieve the effects of easy interpretation, high sensitivity and high sensitivity
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Embodiment 1
[0061] Detection of methylation of SHOX2 and PTGER4 genes in plasma cell-free DNA of patients with stage I lung cancer.
[0062] The kit components are as follows:
[0063]
[0064] Plasma samples from 5 healthy individuals and 5 tumor plasma samples with known pathological information as stage I lung cancer were selected.
[0065] 1. Extract free DNA from the above 10 plasma samples.
[0066] 2. After the extraction of free DNA is completed, bisulfite conversion is performed on the extracted DNA, and the unmethylated cytosine (C) is converted into uracil (U), while the methylated cytosine (C) remains unchanged. Purified Bis-DNA was obtained.
[0067] 3. Prepare PCR reaction solution: DNA polymerase, dNTPs, Mg 2+ , 10×DNA polymerase buffer, SHOX2 and PTGER4 gene 1 primer probe, SHOX2 and PTGER4 gene 2 primer probe, SHOX2 and PTGER4 gene 3 primer probe, internal reference gene primer probe, SHOX2 and PTGER4 gene 1 degenerate blocking primer , SHOX2 and PTGER4 gene 2 dege...
Embodiment 2
[0089] Plasma samples from 93 early lung cancer patients (27 cases at stage 0 and 66 cases at stage I) from Shanghai Lung Hospital and 100 normal human plasma samples from Shandong Qilu Hospital were collected, and the SHOX2 and PTGER4 genes were tested for these 193 plasma samples. For the detection of methylation, the specific operation steps are as described in Example 1. Among the detection results of 100 normal plasma samples, the difference between the target gene 1 / 2 / 3Ct value and the internal reference gene Ct value in 95 samples was greater than 8, and the specificity reached 95%. For 93 early-stage lung cancer plasma samples, 88 The difference between the target gene 1 / 2 / 3Ct value and the internal reference gene Ct value is less than 8, and its sensitivity reaches 95%, including 89% for stage 0 lung cancer and 97% for stage I lung cancer.
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