Application of noncoding gene in diagnosis and treatment of liver cancer
A liver cancer and gene technology, applied in the field of non-coding protein gene LINC01703
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0072] Example 1 Screening for gene markers associated with liver cancer
[0073] 1. Sample collection
[0074] The cancer tissues and paracancerous tissues of 10 patients with liver cancer were collected, and the patients gave informed consent. All the above specimens were obtained with the consent of the organizational ethics committee.
[0075] 2. Preparation of RNA samples
[0076] Tissue RNA was extracted using QIAGEN tissue RNA extraction kit, and the operation was performed according to the specific steps in the manual.
[0077] 3. Reverse transcription and labeling
[0078] The mRNA was reverse-transcribed into cDNA using the Low RNA Input Linear Amplification Kit, and the experimental group and the control group were labeled with Cy3, respectively.
[0079] 4. Hybridization
[0080] The gene chip uses Cannes Bio-Human lncRNA Array, and hybridization is performed according to the steps of the chip instruction manual.
[0081] 5. Data processing
[0082] After hybri...
Embodiment 2
[0085] Example 2 QPCR sequencing to verify the differential expression of LINC01703 gene
[0086] 1. Large-scale QPCR verification of the differential expression of the LINC01703 gene. According to the sample collection method in Example 1, 60 samples of liver cancer tissues and 60 samples of paracancerous tissues were collected.
[0087] 2. The RNA extraction steps are the same as in Example 1.
[0088] 3. Reverse transcription:
[0089] Use 25μl reaction system, take 1μg total RNA for each sample as template RNA, and add the following components to PCR tubes: DEPC water, 5× reverse transcription buffer, 10mM dNTP, 0.1mM DTT, 30μM Oligo dT, 200U / μl M-MLV, template RNA. Incubate at 42°C for 1h, then centrifuge briefly at 72°C for 10min.
[0090] (3) QPCR amplification test
[0091] The amplification primer sequences of LINC01703 and housekeeping gene GAPDH were designed and synthesized by Shanghai Sangong. The primer sequences of LINC01703 gene are shown in SEQ ID NO.2~3;...
Embodiment 3
[0097] Example 3 Analysis of the expression of LINC01703 in the TCGA database
[0098] 1. Data collection
[0099] The lncRNA expression profile data of 200 cases of liver cancer tissues and 50 cases of para-cancerous tissues were collected from the TCGA database, and the expression level of LINC01703 in liver cancer tissues and para-cancerous tissues was analyzed; box plots were drawn.
[0100] 2. ROC curve analysis
[0101] The receiver operating characteristics of LINC01703 were analyzed using the pROC package in R language, the binomial exact confidence space was calculated, and the ROC curve was drawn.
[0102] 3. Results
[0103] The expression level of LINC01703 as figure 2 As shown, compared with the control group, the expression of LINC01703 was significantly up-regulated in liver cancer tissues.
[0104] The ROC curve of LINC01703 is as image 3 As shown, the AUC value of LINC01703 is as high as 0.905, and has high specificity and sensitivity, indicating that L...
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