CN112415199A - Application of CETP detection reagent in preparation of lung cancer screening kit - Google Patents

Application of CETP detection reagent in preparation of lung cancer screening kit Download PDF

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CN112415199A
CN112415199A CN202011316764.3A CN202011316764A CN112415199A CN 112415199 A CN112415199 A CN 112415199A CN 202011316764 A CN202011316764 A CN 202011316764A CN 112415199 A CN112415199 A CN 112415199A
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reagent
cetp
lung cancer
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田攀文
李亚伦
韩青兵
姚梦琳
张立
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West China Hospital of Sichuan University
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Abstract

The invention relates to the field of in-vitro diagnostic reagents, in particular to an application of a CETP detection reagent in preparing a lung cancer screening kit. The invention discovers for the first time that the CETP protein level in plasma exosomes of lung cancer patients is obviously higher than that of healthy people. According to the invention, the reagent for detecting the CETP protein is used for preparing the lung cancer screening kit, so that effective screening of lung cancer can be realized.

Description

Application of CETP detection reagent in preparation of lung cancer screening kit
Technical Field
The invention relates to the field of in-vitro diagnostic reagents, in particular to an application of a CETP detection reagent in preparing a lung cancer screening kit.
Background
Lung cancer is one of the most common malignant tumors in the world, the morbidity and mortality of the lung cancer are on the rising trend year by year, the morbidity is at the top of the world at present, and the health and the life of human beings are seriously threatened.
The lung cancer is a disease good in occult, clinical symptoms are often shown only when the disease develops to the advanced stage, 70-80% of lung cancer patients are already at the middle and advanced stages when the lung cancer symptoms are diagnosed, cancer cells are diffused, the best curing time is missed, and the five-year survival rate is low. For early-stage lung cancer patients, the survival rate and the survival quality of the patients can be greatly improved by 5 years and more through timely treatment. Early diagnosis of lung cancer and effective screening are therefore of paramount importance.
The screening of the lung cancer refers to that the conventional physical examination is carried out on people without lung cancer related symptoms, and the lung cancer is found in time before the symptoms appear. If the lung cancer molecular marker in the plasma can be found, the molecular marker has important significance for prompting a clinician to take relevant treatment measures or decisions for a patient at an early stage.
CETP protein (Unit accession number: P11597) is called Cholesteryl ester transfer protein (Cholesteryl ester transfer protein). The protein is one of the important transporters in lipid metabolism, and mainly mediates the reverse transport process of cholesterol, namely, the continuous exchange of lipid components between High Density Lipoprotein (HDL) particles and other lipoproteins or cell membranes, and simultaneously increases the outflow of cholesterol from tissue cells, so that the cholesterol is transported to the liver. Plasma CETP protein levels are closely related to lipid metabolism balance.
The prior art related to lung cancer of CETP protein is not seen at present.
Disclosure of Invention
The invention aims to provide a novel lung cancer marker and application of a detection reagent of the marker in preparation of a lung cancer screening kit.
The technical scheme of the invention comprises the following steps:
application of a reagent for detecting CETP protein in preparation of a lung cancer screening kit.
As the application, the reagent for detecting the CETP protein is a reagent for enzyme-linked immunosorbent assay.
As for the application, the reagent for detecting the CETP protein is a western blot reagent.
As the application, the reagent for detecting the CETP protein is a reagent for a protein chip detection method.
As for the aforementioned use, the reagent for detecting CETP protein is a reagent for detecting CETP protein in human plasma exosome.
A lung cancer screening kit, which comprises a reagent for detecting CETP protein.
As the kit, the reagent for detecting the CETP protein is a reagent for enzyme-linked immunosorbent assay.
The kit is characterized in that the reagent for detecting the CETP protein is a western blot reagent.
As the kit, the reagent for detecting the CETP protein is a reagent for a protein chip detection method.
As the aforementioned kit, the reagent for detecting CETP protein is a reagent for detecting CETP protein in human plasma exosome.
The key point of the invention is that the content of CETP in human plasma exosomes is determined to be obviously related to the risk of lung cancer, so that the risk of lung cancer can be judged by detecting the content of CETP in human plasma exosomes, and as for the specific means for detecting CETP in human plasma exosomes, various means disclosed in the prior art can be adopted.
The invention provides a new lung cancer screening marker and a new lung cancer screening kit, which can realize effective screening of lung cancer; and the plasma exosome can be used as a detection sample, so that the harm to a patient is low. The invention has good application prospect.
Obviously, many modifications, substitutions, and variations are possible in light of the above teachings of the invention, without departing from the basic technical spirit of the invention, as defined by the following claims.
The foregoing aspects of the present invention are explained in further detail below with reference to specific embodiments. This should not be understood as limiting the scope of the above-described subject matter of the present invention to the following examples. All the technologies realized based on the above contents of the present invention belong to the scope of the present invention.
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FIG. 1: comparison of CETP levels in Lung cancer patients (LC), healthy control (NC) plasma exosomes.
FIG. 2: lung cancer patients (LC) were analyzed by ROC with healthy controls (NC).
Detailed Description
Example 1 relationship of CETP to Lung cancer in plasma
First, clinical data
40 lung cancer patients and 40 healthy controls were selected, and the basic information was as follows:
basic information Patients with lung cancer Healthy controls
Number of people 40 40
Age (age) 58.8±11.5 50.1±14.3
Proportion of male 33(82.5%) 17(44.7%)
Second, detection principle
The method is the same as the basic enzyme-linked immunosorbent assay (ELISA) detection method.
A CETP protein CETP antibody (ASYPDITGEK amino acid sequence (SEQ ID NO.1) for specifically recognizing the CETP protein) is fixed on the protein chip, and after the protein chip is incubated with plasma exosome protein, if the CETP protein exists in the exosome protein, the CETP protein is combined; washing to remove the unbound antibody and other proteins, binding the fluorescence-labeled CETP antibody to the CETP protein for detection, and reading a signal by a fluorescence scanner, wherein the strength of the signal is in positive correlation with the affinity and the quantity of the antibody.
Third, method
1. The preparation method of the plasma exosome protein comprises the following steps:
the sample was removed from-80 ℃ and centrifuged at 12000g for 15 minutes at 4 ℃ and the supernatant was transferred to a new centrifuge tube and filtered through a 0.22. mu.M microporous membrane, and then the exosomes were isolated using PTM-EVs kit manufactured by PTM corporation according to the instructions. Adding Urea with a final concentration of 8M and protease inhibitor for ultrasonic cleavage, and using a BCA kit for protein concentration determination.
2. Plasma exosome CETP protein assay
The reagents were as follows:
Figure BDA0002791074080000031
the method comprises the following steps:
1) rewarming: taking out the chip from a refrigerator at-80 deg.C, putting in a refrigerator at 4 deg.C for rewarming for half an hour, and then putting in room temperature for rewarming for 15 min;
2) and (3) sealing: fixing 14 blocks in the rewarming chip, adding sealing liquid into each block after fixing, placing on a side swing bed, and sealing at room temperature for 3 hr;
3) incubation of exosome protein samples: after the sealing is finished, pouring the sealing liquid completely, then quickly adding the prepared plasma exosome protein incubation liquid, wherein the sample loading volume is 200 mu L, and incubating overnight at 4 ℃ by laterally swinging a shaker at 20rpm (diluting the plasma exosome protein and the incubation liquid in a ratio of 1: 50 to obtain the plasma exosome protein incubation liquid);
4) cleaning: the chip and the chip fence are taken out together, the sample is sucked, then the PBST with the same volume is added rapidly, and the cycle is repeated for a plurality of times, so that no cross contamination among plasma exosome proteins is ensured when the chip fence is detached. After the chip fence is removed, the chip is placed in a chip cleaning box with cleaning solution, and is cleaned for 3 times (10 min each time) by a horizontal shaking table at room temperature of 80 rpm;
5) and (3) secondary antibody incubation: transferring the chip into an incubation box added with 3mL of secondary antibody incubation liquid, laterally swinging a shaker at 40rpm, keeping out of the sun, and keeping at room temperature for 1 hr;
6) cleaning: the chip was removed (note that the upper surface of the chip was not touched or scratched), and placed in a chip washing cassette containing a washing solution, and washed 3 times 10min each time, on a horizontal shaker at room temperature and 80 rpm. After the completion, the mixture is washed for 2 times for 10min by ddH 2O;
7) drying;
8) scanning: scanning by using a crystal core LuxScan 10K microarray chip scanner;
9) data extraction: opening the corresponding GAL file (recording the position of protein in the chip), aligning the chip image and each array of the GAL file integrally, pressing an automatic alignment button, extracting data and storing.
Fourthly, the result
The mean expression level of CETP in lung cancer patient plasma exosomes was 1.02 (protein relative quantitation ratio), and the mean expression level of CETP in healthy control plasma exosomes was 0.56. The lung cancer group was statistically significant compared to the benign lung disease group (p <0.01) (FIG. 1). The lung cancer group and the healthy control have the ROC analysis result that the specificity is 97.5 percent and the sensitivity is 27.5 percent (figure 2); the CETP in the plasma exosome can be shown to distinguish lung cancer from benign lung disease.
The results show that the CETP level difference in the plasma exosomes of the lung cancer patients and the non-lung cancer patients is obvious, and the purpose of screening the lung cancer can be achieved by detecting the CETP level in the plasma exosomes.
EXAMPLE 2 composition of the detection kit of the invention and method of use thereof
Kit composition
Detection kit (14 persons):
Figure BDA0002791074080000041
Figure BDA0002791074080000051
the reagent for preparing the plasma exosome protein needs to be self-prepared, and can be a commercial plasma exosome protein extraction kit.
Second, kit using method
The same as in the third section of example 1.
The kit can screen the risk of lung cancer of the people to be detected by detecting the CETP level in the plasma exosome: if CETP levels are high (relative to healthy controls), the risk of lung cancer is high, and if CETP levels are low, the risk of lung cancer is low. The method can be used for the auxiliary diagnosis of clinical lung cancer, provides effective basis for patients to take relevant treatment measures or decisions, and has good clinical application prospect.
SEQUENCE LISTING
<110> Sichuan university Hospital in western China
<120> GYKH1094-2020P0111926CC20JS044
Application of <130> CETP detection reagent in preparation of lung cancer screening kit
<160> 1
<170> PatentIn version 3.5
<210> 1
<211> 10
<212> PRT
<213> Artificial Sequence (Artificial Sequence)
<400> 1
Ala Ser Tyr Pro Asp Ile Thr Gly Glu Lys
1 5 10

Claims (10)

1. Application of a reagent for detecting CETP protein in preparation of a lung cancer screening kit.
2. The use of claim 1, wherein the reagent for detecting CETP protein is a reagent for enzyme-linked immunosorbent assay.
3. The use of claim 1, wherein the reagent for detecting a CETP protein is a western blot reagent.
4. The use of claim 1, wherein the reagent for detecting a CETP protein is a reagent for a protein chip detection method.
5. The use according to any one of claims 1 to 4, wherein the reagent for detecting a CETP protein is a reagent for detecting a CETP protein in human plasma exosomes.
6. A lung cancer screening kit, which comprises a reagent for detecting a CETP protein.
7. The kit of claim 6, wherein the reagent for detecting CETP protein is a reagent for enzyme-linked immunosorbent assay.
8. The kit of claim 6, wherein the reagent for detecting the CETP protein is a western blot reagent.
9. The kit of claim 6, wherein the reagent for detecting CETP protein is a reagent for a protein chip detection method.
10. The kit of any one of claims 5 to 9, wherein the reagent for detecting a CETP protein is a reagent for detecting a CETP protein in human plasma exosomes.
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