Application of CNTN3 protein in prognosis judgement of neuroglioma
A technique for judging the prognosis of glioma, applied in the field of clinical medicine, to achieve the effect of improving the survival rate of patients, profound clinical significance, and improving the quality of life after surgery
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Embodiment 1
[0025] This example provides the application research of CNTN3 mRNA expression in the prognosis evaluation of human glioma, as follows:
[0026] Patient samples: The present invention involves microarray and sequencing results of 317 cases of glioma and 32 cases of normal brain tissue. Among them, the expression profile chip GSE4290 included 81 cases of glioma and 23 cases of normal brain tissue, and the expression profile chip GSE7696 included 80 cases of glioma and 4 cases of normal brain tissue, which were obtained from the GEO database (https: / / www.ncbi. nlm.nih.gov / geo / ); Another 156 cases of glioma and 5 cases of normal brain tissue sequencing data and detailed clinical information data come from the Tumor Genome Atlas (TCGA) (https: / / cancergenome.nih.gov / ). The overall survival time was defined as the time from the diagnosis of glioma to the death of the patient or the end of follow-up.
[0027] Analysis method: Download chip and sequencing data compression packages ...
Embodiment 2
[0037] This example gives the application research of CNTN3 protein expression in the prognosis evaluation of human glioma, as follows:
[0038] Patient samples: tissue chips from Shanghai Xinchao Biotechnology Co., Ltd. (product number: HBraG080PG01), including 13 normal brain tissues and 67 glioma tissue samples.
[0039]Detection method: Bake the front side of the tissue chip in a 65°C oven for 40 minutes to make the specimen adhere better, immerse in xylene washing tanks I, II, and III, and place them in a constant temperature water bath at 25°C for 10 minutes. Transfer to 100%, 85%, and 75% ethanol for gradient hydration for 3 minutes each, then transfer to PBS buffer I, II, III for 5 minutes each time, place in 3% hydrogen peroxide washing tank for 15 minutes, and block the endogenous sex peroxidase. Immerse in the heated sodium citrate buffer, and microwave for 20 minutes on low heat. Immerse in PBS buffer I, II, III for 3 minutes each time. Draw the area along the e...
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