Method for detecting PTEN (Phosphatase and tensin homolog) gene and PI3K/AKT protein and application of method in cancer treatment
A protein and gene technology, applied in the field of detection of PTEN gene and PI3K/AKT protein, can solve the problem of low objective response rate, and achieve the effect of preventing missed treatment opportunities and economic losses, and accurate test results.
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Embodiment 1
[0054] A method for detecting PTEN gene, said detection method comprising the following steps:
[0055] DNA sequencing operations
[0056] 1) Total DNA extraction: Take 1cm of fresh breast tissue (including cancer tissue and paracancerous tissue) from patients with breast cancer (female A and woman B) 3 ×1cm 3 ×1cm 3 Size, wash with normal saline 3 times, and cut the tissue with scissors, add DNA extraction buffer (0.33M NaAc, 25mM EDTA, pH 6.4), 10% SDS and proteinase K (10mg / ml), 55 ℃ water bath 3h, during the water bath, mix by inversion; after the water bath, add 500μl isopropanol to the tissue, gently invert and mix for 10min, then centrifuge at 12000rpm for 15min, discard the supernatant, the precipitate is the DNA precipitate, and air dry the DNA precipitate Finally, 100 μl of TE buffer was added to the DNA precipitation to dissolve the DNA precipitation, and the concentration of the DNA was measured in a Nano Drop (DNA UV spectrophotometer, GENE, USA), and the ratio...
Embodiment 2
[0076] A method for detecting PI3K / AKT protein, said detection method comprising the following steps:
[0077] Western Blotting operation
[0078] 1) Take fresh breast tissue from patients with breast cancer (female A and female B), place the tissue on ice, and separate the tissue with a sterilized pre-cooling tool to obtain tissue blocks;
[0079] 2) Put the tissue block into a round-bottomed Eppendorf tube, add liquid nitrogen to the tube to freeze the tissue block, place the Eppendorf tube on ice, and grind it evenly to obtain tissue grinds;
[0080] 3) Add lysis buffer to the tissue ground material, the amount of the lysis solution added is 60 μl / mg, homogenize in ice bath, and then shake the Eppendorf tube at 4°C for 2 hours to obtain a homogeneous tissue Slurry, the protein concentration in the tissue homogenate reaches at least 0.1 mg / ml; the lysis buffer is purchased from Beyontian Company;
[0081] 4) Centrifuge the tissue homogenate at 4°C for 20 minutes at a speed...
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