Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Method for rapidly detecting EGFRvIII mutation

A fast, probe-based technology, applied in the fields of cancer detection and molecular biology, can solve problems such as weak correlation, achieve the effects of avoiding pollution, accurate and reliable experimental results, and streamlined operations

Pending Publication Date: 2020-11-27
杭州布平生物医药科技有限公司
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Immunohistochemistry or Western Blot is an important way to detect the protein level expression of EGFRvIII, but many studies have shown that the correlation between EGFRvIII protein level expression and nucleic acid level is weak

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for rapidly detecting EGFRvIII mutation
  • Method for rapidly detecting EGFRvIII mutation
  • Method for rapidly detecting EGFRvIII mutation

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] A method for rapid detection of EGFRvIII mutation, comprising the following steps:

[0023] (1) extract the RNA of the tumor tissue of sample 1;

[0024] (2) Construct PCR reaction system;

[0025] (3) Real-time fluorescent quantitative PCR was carried out by TaqMan probe method;

[0026] (4) Interpretation of results.

[0027] Further, the extraction steps for sample 1 RNA are as follows: paraffin sample dewaxing: take five 7 μm sample 1 paraffin tissue sections and put them into a 1.5ml centrifuge tube, add 1ml xylene, centrifuge at 13,000xg for 1 minute, discard the supernatant, and then Add 1ml of xylene, centrifuge at 13,000xg for 1 minute, and discard the supernatant. Add 1ml of absolute ethanol to the centrifuge tube, centrifuge at 13,000xg for 1 minute, discard the supernatant, and dry it; add tissue lysate and proteinase K to the dried tissue, lyse at 56°C for 15 minutes, and transfer the centrifuge tube to Keep it at 80°C for 15 minutes and take it off. Wh...

Embodiment 2

[0039] A method for rapid detection of EGFRvIII mutation, comprising the following steps:

[0040] (1) extract the RNA of sample 1 tumor tissue;

[0041] (2) construct PCR reaction system;

[0042] (3) Real-time fluorescent quantitative PCR was carried out by TaqMan probe method;

[0043] (4) Interpretation of results.

[0044] Further, the extraction steps for sample 1 RNA are as follows: paraffin sample dewaxing: take five 7 μm sample 1 paraffin tissue sections and put them into a 1.5ml centrifuge tube, add 1ml xylene, centrifuge at 13,000xg for 1 minute, discard the supernatant, and then Add 1ml of xylene, centrifuge at 13,000xg for 1 minute, and discard the supernatant. Add 1ml of absolute ethanol to the centrifuge tube, centrifuge at 13,000xg for 1 minute, discard the supernatant, and dry it; add tissue lysate and proteinase K to the dried tissue, lyse at 56°C for 15 minutes, and transfer the centrifuge tube to Keep it at 80°C for 15 minutes and take it off. When it r...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a method for rapidly detecting EGFRvIII mutation. EGFRvIII RNA is used as a starting template of a reaction, redundant intron sequences in an EGFRvIII DNA sequence are avoided,and a probe crosses a fusion site of an EGFRvIII exon, so that interference of genome DNA is effectively avoided, and a detection result is more accurate; reverse transcription and real-time PCR share one reaction system, which avoids pollution possibly caused by repeated cover opening compared with traditional detection that carries out amplification by using cDNA as a template after reverse transcription; by changing fluorophores, a housekeeping gene ACTB is introduced into a single system, so that the risk of false negative is reduced, and the risk of false positive is reduced by identifying the result of [delta]Ct; a designed PCR product is relatively small, so that a paraffin-embedded sample with a high degradation degree can meet detection requirements, and meanwhile, the detectionresult can be in correspondence with an EGFRvIII immunohistochemical result of the same tissue sample. The method is simple in operation, and guarantees credibility and accuracy of the detection result.

Description

technical field [0001] The invention relates to the fields of cancer detection and molecular biology, especially a method for rapidly detecting EGFRvIII mutation. Background technique [0002] Malignant tumors are currently one of the diseases that seriously affect human health. The internal cause of malignant tumors is that changes in genes in cells lead to abnormal regulation of cell growth, resulting in abnormal proliferation and tumor formation. Many studies have shown that the EGFR (Epidermal Growth Factor Receptor) protein, one of the members of the surface growth factor receptor family, is related to the regulation mechanism of inhibiting tumor cell proliferation, angiogenesis, tumor invasion, metastasis and apoptosis. By binding to ligands, EGFR receptors can activate downstream signaling channels to regulate physiological processes such as cell growth, proliferation, and differentiation. Therefore, excessive activation of EGFR signaling pathways will lead to uncontr...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/6851C12Q1/6886
CPCC12Q1/6851C12Q1/6886C12Q2600/158C12Q2600/156C12Q2531/113C12Q2561/101C12Q2563/107
Inventor 相学平陈柯冰秦樾童莹慧
Owner 杭州布平生物医药科技有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products