CircRNAs associated with mtx drug resistance of tumor cells and their application in reversing mtx drug resistance of tumor cells
A tumor cell and drug resistance technology, applied in the field of tumor biodiagnosis and treatment, to achieve the effect of reversing tumor drug resistance, reducing the degree of gene amplification and improving efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1c
[0041] Example 1 Differential expression of circRNA7746 in MTX-sensitive and drug-resistant cells
[0042] 1. Screening differentially expressed circular RNAs in HT-29 MTX sensitive cells and HT-29 MTX resistant cells containing DMs
[0043] (1) Cell culture
[0044] The HT-29 MTX sensitive cell line was cultivated with DMEM high glucose medium containing 15% fetal bovine serum, and the final concentration of MTX was 10 -4 mol / L medium to culture HT-29 MTX drug-resistant cell line containing DMs. All cells were cultured in 5% CO 2 , 37 ℃ cell culture incubator.
[0045] Entrusted Beijing Nuohezhiyuan Company to conduct HT-29 MTX sensitive cells and HT-29 10 -4 mol / L MTX drug-resistant cell lines (each cell provided three independent biological replicates) were independently constructed for circular RNA, followed by next-generation sequencing. Identification of circular RNAs using the find_circ bioinformatics method. The relative expression of circular RNA in each sample ...
Embodiment 2
[0115] Example 2 Effect of interfering with circRNA7746 on cell drug resistance
[0116] 1. Establishment and verification of DMs-containing HT-29MTX drug-resistant cell interference circRNA7746 clone
[0117] (1) HT-29MTX drug-resistant cells containing DMs interfered with the establishment of circRNA7746 clones.
[0118] Firstly, the optimal purine concentration was screened in HT-29 MTX drug-resistant cells containing DMs. The HT-29 MTX drug-resistant cells containing DMs in the logarithmic growth phase were digested with trypsin for 5 minutes, and then resuspended with medium to form a single cell suspension. After cell counting, 10 5 Cells were inoculated into a 24-well plate at a density of 24 cells, shaken evenly in a cross method, and placed in an incubator for cultivation to adhere to the wall. After culturing for 24 hours, replace the fresh medium, and add different amounts of puromycin to each well in turn, so that the final concentrations of puromycin in the medi...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com