Application of circ_2157 in the preparation of nasopharyngeal carcinoma treatment preparations and therapeutic preparations
A nasopharyngeal carcinoma and preparation technology, applied in the field of tumor molecular biology, can solve problems such as unclear molecular mechanism and insignificant curative effect
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Embodiment 1
[0085] Example 1: Expression of circ_2157 in nasopharyngeal carcinoma tissues and cells
[0086] 1. According to the standard sample collection plan, we collected 41 tissue samples from patients with nasopharyngeal carcinoma from Hunan Cancer Hospital. All the cases were newly diagnosed patients in the Department of Head and Neck Surgery of Hunan Cancer Hospital (time interval: January 2016 to November 2016). 29 cases of nasopharyngeal carcinoma and 12 cases of nasopharyngeal inflammation were diagnosed by the pathology department (neoplastic diseases, no active infectious diseases, severe immune diseases and other major diseases have been excluded).
[0087] Complete personal information and clinical data were recorded during the collection process, including name, gender, age, outpatient number, hospitalization number, pathological type, case stage, and EBV infection, etc. See the screenshot of the Excel spreadsheet for details. All samples are collected with the permission...
Embodiment 2
[0124] Example 2: Detection of overexpression effect of circ_2157 in nasopharyngeal carcinoma cell lines
[0125] First, we selected the restriction site, put the full-length sequence of circ_2157 into the NEB cutter 2.0 online website for analysis, and showed that the ClaI and SacII restriction sites were sites that did not exist in the full-length sequence of circ_2157, and at the same time in the pcDNA3.1 plasmid vector ( Purchased from Invitrogen Corporation) DNA restriction endonuclease that exists alone. Construct an overexpression vector accordingly; figure 2 The overexpression vector map drawn for.
[0126] In order to test the circling efficiency of circ_2157, we first expressed the constructed pcDNA3.1 / circ_2157 eukaryotic overexpression vector in nasopharyngeal carcinoma cells. The third and fourth generation nasopharyngeal carcinoma cells HONE1, HNE2 and CNE2 in good growth condition were seeded into 12-well plates, and when the cell confluence reached 60%-80%, ...
Embodiment 3
[0127] Example 3: Detection of the effect of silencing circ_2157 expression in nasopharyngeal carcinoma cell lines
[0128]The SI sequence of circ_2157 was designed according to the splicing site. siRNA is a kind of double-stranded RNA molecule with a length of 21-25 nucleotides, which can complementarily bind with homologous RNA, specifically degrade the target RNA, and thereby inhibit its expression. At present, siRNA has developed into an important tool for the study of gene function. In order to explore the role of circ_2157 in tumorigenesis and development, we designed siRNA according to the splicing site of circ_2157, and transiently transfected siRNA and siNC (blank control) into HONE1, HNE2 and CNE2 cell lines with Hiperfect reagent to silence the expression of circ_2157. Continue to culture for 48 hours after transfection to collect cells, use real-time fluorescent quantitative PCR technology to detect the expression level of circ_2157 to detect the transfection effic...
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