Application of miRNA combined marker to preparation of kit for diagnosing or detecting HBV+ and LC-primary HCC
A marker and primary technology, applied in the field of molecular biology and medical diagnosis, can solve the problems of lack of pertinence and complex pathogenesis of liver cancer, achieve excellent sensitivity and specificity, convincing detection results, and reduce errors. Effect
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Embodiment 1
[0019] Example 1 Subject and Sample Extraction
[0020] The samples were provided by Singapore General Hospital (approved by Singapore SingHealth CIRB B, approval number CIRB Ref: 2007 / 447 / B). Among them, there were 34 HCC patients with HBV+ / LC-, and 89 non-HCC patients with HBV+ / LC-.
Embodiment 2
[0021] Example 2 Extraction of exosomes
[0022] Collect 2ml of peripheral blood from the subject with a disposable syringe, quickly transfer it to an EDTA anticoagulant tube, and mix well. Separate the plasma within 2 hours of collection. The specific steps are: 1) transfer the whole blood to a 2ml centrifuge tube, and centrifuge at 500g for 10min at room temperature; 2) take the upper plasma, and centrifuge at 2000g for 10min at 4°C; 3) take the upper plasma, 4°C, Centrifuge at 16,000 g for 10 min; 4) The separated plasma is directly used for exosome extraction or frozen in a -80°C refrigerator.
[0023] Exosomes were extracted according to the instructions of the exosome extraction kit Exo-Quick exosome precipitation solution (EXOQ5SA-1, SBI, United States). 1) Add the plasma to a centrifuge tube, and add Exo-Quick at a ratio of 63 μl for every 250 μl of plasma; 2) Centrifuge at 1500 g at 4°C for 30 minutes, discard the supernatant; 3) Centrifuge at 1500 g at 4°C for 5 min...
Embodiment 3
[0024] Example 3 Extraction of exosome miRNA
[0025] miRNA was extracted according to the operating instructions of the miRNeasy Serum / PlasmaKit kit (217184, QIAGEN, Germany). The specific steps are: 1) Add 5 times the volume of QIAzol LysisReagent to the plasma separated in Example 2, vortex or pipette to mix; 2) Incubate at room temperature for 5 minutes; 3) Add an equal volume of chloroform and shake for 15 seconds; 4) Incubate at room temperature for 2-3min; 5) Centrifuge at 12000g for 15min at 4°C; 6) Transfer the upper layer to a new centrifuge tube, add 1.5 times the volume of absolute ethanol, and mix by pipetting to obtain the sample; 7) Take 700μl sample to RNeasy MinElute Spin column (placed in a 2ml collection tube), cover the lid, centrifuge at room temperature>8000g for 15s, discard; 8) repeat step 7 once; 9) add 700μl RWTbuf to the RNeasy MinElute spin column, centrifuge at room temperature>8000g for 15s, discard ;10) Add 500μl RPE buf to the RNeasy MinElute s...
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