Application of ythdf2 gene in diagnosis, prevention and treatment of urothelial carcinoma
A urothelial cancer, gene technology, applied in the field of biomedicine, to achieve the effect of promoting proliferation and migration
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Embodiment 1
[0023] Example 1, RT-qPCR detection of differential expression of YTHDF2 gene in urothelial carcinoma tissue
[0024] A total of 39 urothelial carcinoma tissues and corresponding paracancerous tissues were collected. The informed consent of the patients was obtained for the tissue samples and the approval of the organizational ethics committee was obtained. Use Ambion's Trizol reagent to extract RNA samples, and the specific steps are detailed in the instructions. The concentration and purity of the extracted RNA were detected by Nanodrop2000. 1 μg of RNA was used for reverse transcription, and cDNA was obtained by reverse transcription using Vazyme's HiScript Q RT SuperMix. Primers were designed according to the sequences of YTHDF2 gene and RPL13A gene, and the primer sequences were synthesized by Shanghai Sangong. The designed primer sequences are as follows:
[0025] YTHDF2 forward primer: 5'-AGCCCCACTTCCTACCAGATG-3'
[0026] YTHDF2 reverse primer: 5'-TGAGAACTGTTATTTCCC...
Embodiment 2
[0030] Example 2, Differential expression of YTHDF2 gene in human urothelial carcinoma cell lines
[0031] Human urothelial carcinoma cell lines SW780 and UM-UC-3 were cultured in DMEM medium, human urothelial carcinoma cell lines T24 and 5637 were cultured in 1640 medium, and the immortalized bladder tissue cell line Sv-huc-1 was cultured in DMEM / F-12. Culture conditions are 37°C, 5% CO 2 , 90% humidity. The medium was changed in 2 days, the vigorously growing cells were collected, RNA was extracted and reverse-transcribed to obtain cDNA, and RT-qPCR was used to detect the expression of YTHDF2 gene in urothelial carcinoma cell lines. The result is as figure 2 As shown, YTHDF2 gene expression was upregulated in urothelial carcinoma cell lines SW780, UMUC3, T24 and 5637 compared with normal bladder cell lines.
Embodiment 3
[0032] Embodiment 3, the construction of YTHDF2 knockout cell line
[0033] Design sgRNA according to YTHDF2 gene sequence, the designed sgRNA primer sequence is as follows:
[0034] sgRNA1 forward primer: 5'-CACCGTCCATTACTAGTAACATCG-3'
[0035] sgRNA1 reverse primer: 5'-AAACCGATGTTACTAGTAATGGAC-3'
[0036] sgRNA2 forward primer: 5'-CACCGAGTTACTACAGTCCCTCCAT-3'
[0037] sgRNA2 reverse primer: 5'-AAACATGGAGGGACTGTAGTAACTC-3'
[0038] Dissolve the above primers in ddH 2O to a final concentration of 100 μM, add 1 μl of forward and reverse primers to 8 μl ddH 2 In O, annealing was carried out according to the following procedure: 37°C for 30 min, 95°C for 5 min, and cooling down to 25°C at a rate of 0.8°C / s. Take 1 μl of the annealed primer and connect it to the lenticrisprV2 vector. The plasmid carrying YTHDF2 sgRNA was transferred into SW780 and T24 cells by lentivirus, and puromycin was added, and a monoclonal cell line with YTHDF2 knockout was obtained by screening.
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