A SNP marker related to auxiliary diagnosis of breast cancer and its application
An auxiliary diagnosis and marker technology, applied in the fields of genetic engineering and oncology
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0067] The collection of embodiment 1 sample and the arrangement of sample data
[0068] From January 2004 to April 2010, the inventor collected a large number of blood samples from patients with new-onset breast cancer in a hospital in Jiangsu Province. After sorting out the sample data, the inventor selected 2137 samples that met the following criteria. Experimental samples for microarray scanning and single SNPSequenomMassARRAY genotyping:
[0069] 1. Breast cancer cases diagnosed by pathology;
[0070] 2. Have not received radiotherapy or chemotherapy before blood collection, and have no previous history of cancer;
[0071] 3. Healthy female controls matched with the age of the case
[0072] The demographic data and clinical data of these samples were collected systematically.
Embodiment 2
[0073] Example 2 Whole Exome Detection of SNP in Peripheral Blood DNA
[0074] Among the 1064 eligible breast cancer patients and 1073 healthy female controls mentioned above, the two groups were balanced and comparable in age. The two groups of people were detected by the whole exome microarray to obtain relevant results. The specific steps are:
[0075] 1. Add hemolysis reagent (i.e., lysate, 40 parts) to the peripheral blood stored in a 2ml cryopreservation tube. The volume of the solution was adjusted to 2000ml, the same below), and it was completely transferred after inverting and mixing.
[0076] 2. Removal of red blood cells: Fill the 5ml centrifuge tube to 4ml with hemolysis reagent, mix by inverting, centrifuge at 4000rpm for 10 minutes, and discard the supernatant. Add 4ml of hemolysis reagent to the precipitate, invert and wash again, centrifuge at 4000rpm for 10 minutes, and discard the supernatant.
[0077]3. Extract DNA: Add 1ml of extract solution to the pre...
Embodiment 3
[0087] Example 3 SequenomMassARRAY genotyping of a single SNP
[0088] The SNPs found to be significantly associated with breast cancer in the above whole exome scan were detected on the SequenomMassARRAY genotyping platform. The specific steps were as follows:
[0089] 1. Add the hemolysis reagent to the peripheral blood stored in the 2ml cryopreservation tube, mix it upside down and transfer it completely.
[0090] 2. Removal of red blood cells: Fill the 5ml centrifuge tube to 4ml with hemolysis reagent, mix by inverting, centrifuge at 4000rpm for 10 minutes, and discard the supernatant. Add 4ml of hemolysis reagent to the precipitate, invert and wash again, centrifuge at 4000rpm for 10 minutes, and discard the supernatant.
[0091] 3. Extract DNA: Add 1ml of extract solution and 8μl of proteinase K to the precipitate, shake and mix well on the shaker, and bathe in 37°C water overnight.
[0092] 4. Remove protein: add 1ml of saturated phenol and mix well (shake gently by h...
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