Marker for monitoring disease progression of gliocytoma
A glioblastoma and material technology, applied in the field of markers for monitoring the progress of glioblastoma, can solve the problem that the prognosis of glioblastoma patients has not been significantly improved
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Embodiment 1
[0062] Embodiment 1, detect the primer design of DILC gene expression level
[0063] Download the nucleic acid sequence of the long non-coding RNA DILC in GeneBank, select the DNA molecule shown in Sequence 1 (152-393 of the DILC gene) as the target sequence for real-time quantitative PCR, design and synthesize the DILC gene for real-time quantitative PCR detection Sequence-specific primers, the primer sequences are as follows:
[0064] Upstream primer: f1:5'-CAGAACCTTAGTCCCGGGAA-3' (SEQ ID No.2);
[0065] Downstream primer: r1:5'-CGTCTGCCACTTCGTTGTAG-3' (SEQ ID No. 3).
Embodiment 2
[0066] Example 2, the application of DILC gene as a marker of glioblastoma disease progression
[0067] 1. Detection of DILC gene expression level by real-time quantitative PCR
[0068] 1. Glioblastoma case and control samples
[0069] All 43 cases of glioblastoma were donated by the Second Hospital of Hebei Medical University, China. According to the 2007 World Health Organization (WHO) pathological grading standard, 43 cases of glioblastoma were grouped as follows: I / II grade, 23 cases; III grade, 7 cases; IV grade, 6 cases. Tissue samples from 43 glioblastoma cases collected from medical donations were obtained after approval by the local medical ethics committee, and were stored in liquid nitrogen for use in experiments.
[0070] A total of 7 cases of normal control samples.
[0071] 2. Acquisition of cDNA
[0072] (1) Extraction of RNA
[0073] Grind the clinical tissue samples from step 1 to extract RNA. For the extraction method of RNA, please refer to the instruc...
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