Applications of LncRNA for diagnosing patients with breast cancer chemotherapy-related myocardial injury
A technology for myocardial injury and breast cancer, which is applied in the field of biomedicine to achieve the effect of reducing the possibility of myocardial injury, high sensitivity and specificity
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Embodiment 1
[0024] Example 1 Screening for differential expression of long non-coding RNAs in breast cancer chemotherapy-related myocardial injury
[0025] 1. Research object
[0026] The blood of 5 breast cancer patients with myocardial injury after chemotherapy was selected (group B), and the blood of corresponding breast cancer patients before chemotherapy (group A) (patients without myocardial injury before chemotherapy) were selected. At the same time, 5 cases of breast cancer after chemotherapy were selected. The blood of patients without myocardial injury (group D) and the blood of corresponding breast cancer patients before chemotherapy (group C) were reviewed and approved by the hospital ethics committee, and all patients signed a written informed notice before enrollment.
[0027] 2. RNA extraction
[0028] (1) After clinical serum samples are collected, put them in a centrifuge, centrifuge at 12000r / min for 10min, repeat twice, and store the obtained serum samples in a -80°C r...
Embodiment 2
[0045] Example 2 Real-time quantitative PCR to verify the expression difference of LINC01471 gene
[0046] 1. Sample selection
[0047] The blood of 20 breast cancer patients with myocardial injury after chemotherapy (group B) and the blood of corresponding breast cancer patients before chemotherapy (group A) (group A) (patients without myocardial injury before chemotherapy) were selected. This study was reviewed by the hospital ethics committee All patients signed a written informed notice before enrollment.
[0048] 2. Fluorescent quantitative PCR detection
[0049] (1) The extraction steps of serum RNA are the same as in Example 1
[0050] (2) Reverse transcription reaction
[0051] Genomic DNA removal
[0052] Reagent
[0053] Reagent Usage amount 5×gDNA Eraser Buffer 2.0 μl gDNA Eraser 1μl Total RNA 1μg RNase Free dH2O up to 10 μl
[0054] Reaction conditions
[0055] 2 minutes at 42°C, 4°C.
[0056] reverse transcriptio...
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