Methylation site in the promoter region of eno1 gene and its application in the preparation of kits for early diagnosis and prognosis evaluation of esophageal cancer
A gene promoter region and early diagnosis technology, applied in biochemical equipment and methods, recombinant DNA technology, microbial measurement/inspection, etc., can solve the problem of lower overall survival rate of patients, and achieve far-reaching clinical significance and promotion value. Good specificity and easy operation
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Embodiment 1
[0071] Methylation changes of ENO1 gene in esophageal squamous cell carcinoma and its clinicopathological significance
[0072] 1. DNA preparation: The tumor tissues of 68 patients with esophageal squamous cell carcinoma and their corresponding 62 adjacent normal tissues were selected, fixed in formalin and embedded in paraffin. The paracancerous normal tissues were all paraffin blocks of esophageal normal tissues and were selected from samples at a distance of more than 2 cm from the esophageal squamous cell carcinoma. Genomic DNA was extracted with QIAamp DNA FFPE Tissue Kit, and its content and purity were determined by UV spectrophotometer to determine the absorbance value, and gel electrophoresis was used to ensure the quality of the extracted DNA.
[0073] 2. Bisulfite treatment: Use EZ-96DNA Methylation-Gold™ Kit for bisulfite modification. The obtained DNA was used immediately or stored at -20°C for later use.
[0074] 3. PCR amplification reaction: Design primers fo...
Embodiment 2
[0129] Expression of ENO1 protein in esophageal squamous cell carcinoma tissue and adjacent normal.
[0130] The expression of ENO1 protein in 273 cases of esophageal squamous cell carcinoma and 263 cases of adjacent normal tissues was detected by immunohistochemistry.
[0131] The prepared esophageal cancer tissue chip paraffin block was taken for 4 μm serial sections, and the immunohistochemical method of the tissue chip was the same as the conventional method. This experiment adopts the two-step immunohistochemical Envision method, and the specific steps are as follows:
[0132] (1) Before the experiment, put the prepared 4μm white slices into the slicing box and store them in a 4°C refrigerator for subsequent experiments;
[0133] (2) Before the experiment, insert the white slices of the tissue chips stored in the refrigerator at 4°C into the metal basket and bake them in a 60°C oven for 1.5-2 hours to prevent the tissue from falling off;
[0134] (3) Put the paraffin ti...
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