Peripheral blood TCR marker for prostate cancer, and detection kit and application thereof
A technology of prostate cancer and markers, applied in the field of genetic engineering, can solve the problems of over-diagnosis of prostate cancer, missed opportunities for canceration, over-treatment, etc., and achieve the effects of lower detection costs, simple sampling, high specificity and accuracy
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Embodiment 1
[0043] Example 1 Obtaining Prostate Cancer TCR Marker CDR3 Sequence Set by Immunogram Analysis
[0044] 1. Sampling and immune map analysis (method reference patent ZL201910300069.9)
[0045] Collect 1301 control groups (including healthy people and patients with non-tumor diseases, 1300 people for model building, 1 healthy person for verification), 11 prostate cancer patients (10 people for model building, 1 person for verification) and the peripheral blood of a subject with unknown health status (10mL per person), and the amino acid sequence of the TCR epitope 3 (CDR3) of the subject and the control group was obtained by high-throughput sequencing to ensure the functionality of each sample The total number of CDR3 sequences of TCR should not be less than 30,000;
[0046] 2. The CDR3 sequences of the TCR of each sample are randomly sampled without replacement, so that the total number of CDR3 sequences of each sample is 30,000. For any specific CDR3 sequence X, the number o...
Embodiment 2
[0052] Example 2 Verification of the specificity of the prostate cancer TCR marker CDR3 sequence set
[0053] 1. Sampling and immune map analysis (method reference patent ZL201910300069.9)
[0054] Peripheral blood (10 mL per person) was collected from 339 non-prostate cancer tumor patients and 2 subjects with unknown health status, and the epitope 3 (CDR3) amino acid of TCR in the subjects and the control group was obtained by high-throughput sequencing Sequences, to ensure that the total number of CDR3 sequences of functional TCRs in each sample is not less than 30,000; random non-replacement sampling is performed on the CDR3 sequences of TCRs in each sample, so that the total number of CDR3 sequences in each sample is 30,000.
[0055] 2. Randomly select 100 healthy people and 45 non-tumor disease patients from the control group in Example 1.
[0056] 3. According to 100 healthy people, 45 non-tumor disease patients, 10 prostate cancer patients from embodiment 1, and 339 no...
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