Application of exosome TβRII protein as a marker in the preparation of breast cancer detection kit

Abstract

The present invention discloses an application of the exosome TβRII protein as a marker in preparing a breast cancer diagnostic kit, and belongs to the technology field of breast cancer detection kits. The present invention finds that the content of TβRII positive exosomes in the serum of breast cancer patients is significantly higher than these of healthy people, and after the surgery, the content of TβRII exosomes in the serum of breast cancer patients reduces significantly, which suggests the value of the TβRII positive exosomes during the diagnosis and prognosis of breast cancer. The present invention provides a breast cancer diagnosis kit based on detecting exosome TβRII protein in peripheral blood, which is simple in operation, and only needs to extract a small amount of peripheral blood of the test population, thereby detecting whether the test population has breast cancer and evaluating the tumor of the patient. The degree of malignancy and the state of metastasis.

Claims

1. A breast cancer detection kit based on the detection of TβRII protein in peripheral blood exosomes, which comprises a direct-labeled primary antibody against TβRII protein and a TβRII positive exosome standard, wherein the TβRII positive exosome standard is isolated from a breast cancer cell line MDA-MB-231 cell culture supernatant.

2. The breast cancer detection kit according to claim 1, wherein the direct-labeled primary antibody is marked with APC.

3. The breast cancer detection kit according to claim 1, wherein the breast cancer detection kit comprises a sodium citrate anticoagulant, and the sodium citrate has a mass percentage concentration of 2.5%.

4. The breast cancer detection kit according to claim 1, wherein the breast cancer detection kit comprises a PBS buffer.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows the results of immunoblotting of human breast cancer cell MDA-MB-231 exosomes TβRII protein content.

(2) FIG. 2 shows the results of electron microscopy of TβRII protein content in human breast cancer cell MDA-MB-231 exosomes.

(3) FIG. 3 shows the results of flow cytometry of human breast cancer cell MDA-MB-231 exosomes TβRII protein content.

(4) FIG. 4 is the diameter (A) of the isolated exosomes detected by nanosight, density (B) and the shape of the exosomes (C) taken by electron microscopy.

(5) FIG. 5 is an exosome particle with an exosomal marker protein photographed with an electron microscope.

(6) FIG. 6 shows the results of flow cytometry analysis of TβRII protein content in peripheral blood exosomes of breast cancer patients and normal subjects.

(7) FIG. 7 is a graph showing the results of comparison of TβRII protein content in peripheral blood exosomes of breast cancer patients and normal subjects.

(8) FIG. 8 is a graph showing the results of sensitivity and specificity analysis of peripheral blood exosomes TβRII protein in breast cancer patients and normal subjects.

(9) FIG. 9 is a schematic diagram showing the flow of peripheral blood exosomes from preoperative and postoperative patients (A) and the comparison of TβRII protein content in peripheral blood exosomes (B).

(10) FIG. 10 shows the results of electron microscopy of TβRII protein in peripheral blood exosomes of patients with breast cancer before and after surgery.

THE DETAILED DESCRIPTION OF THE EMBODIMENTS OF THE INVENTION

(11) In order to more fully understand the technical content of the present invention, the technical solution of the present invention will be further described below in conjunction with experiments.

Embodiment 1

(12) 1. Exaction and identification of exosome derived from human breast cancer cell line MDA-MB-231. The extraction method is as follows:

(13) MDA-MB-231 cell culture supernatant was prepared, centrifuged at 4000 rpm/min for 10 min; the supernatant was collected and centrifuged at 100,000 g for 1 hour; the pellet was collected, and the pellet was resuspended in 28 ml of PBS buffer and centrifuged at 100,000 g for 1 hour. For exosomes. The exogenous body weight was suspended in 0.2 ml of PBS buffer and stored in −80° C. for use.

(14) 2. exosomes lysate lysis (composition: 2.5% SDS and 8 M urea, the balance is water) exosomes 30 minutes, determination of exosome concentration by BCA protein concentration; determination of isolated products by immunoblotting Tumor exosomes.

(15) As shown in FIG. 1, the isolated exosomes of step 1 contained a high protein content of TβRII in addition to the known markers TSG101, ALIX, and CD63.

(16) 3. Detection of exosomal TβRII by flow cytometry:

(17) (1) APC-TβRII direct standard primary antibody (R&D Systems: Catalog #FAB241A) was added to the exosomes in a ratio of 1:100, and incubated for 30 minutes at room temperature in the dark, and washed three times with PBS;

(18) (2) The average fluorescence intensity of TβRII in exosomes was determined by flow cytometry.

(19) Model loading, adjusting and determining the instrument's forward angular scattered light, side angle scattered light and FL1 basic parameters, FSC adopts Line linear form, SSC and FL1 adopt Log logarithm form, and FSC-H/SSC-H scatter The exosomes were circled on the graph, and the excitation light was selected at 633 nm. The fluorescence value of the exosomes was obtained in the FSC/APC scattergram, and more than 10,000 exosomes were read, and the scattergram was analyzed.

(20) 4. The identification of MDA-MB-231 cell exosomes by electron microscopy showed that the prepared exosomes were small vesicles with a diameter of about 100 nm, with typical lipid bilayer structure and high TβRII content. (FIG. 2). The results of flow cytometry also showed that the content of TβRII in MDA-MB-231 cells was higher (FIG. 3).

Embodiment 2

(21) Using the technique of Example 1, the peripheral blood exosomes of 36 breast cancer patients (20 normal samples were also tested as negative controls) were isolated and obtained and identified, and the expression of TβRII was detected.

(22) 1. Using ultracentrifugation to obtain exosomes in the peripheral blood of the population to be tested:

(23) 1 ml of venous blood from each sample was collected, 0.5 ml of 2.5% sodium citrate anticoagulant was added, mixed well, centrifuged at 4000 rpm/min for 10 min, and the upper layer of plasma was taken.

(24) PBS was added to dilute the upper layer plasma to 28 ml, poured into an ultracentrifuge tube, and centrifuged at 100,000 g for 1 hour. The supernatant was discarded with a pipette or pipette, 1 ml of liquid was left at the bottom of the tube, PBS was added to 28 ml, the pellet was resuspended, and centrifuged at 100,000 g for 1 hour. The supernatant was discarded with a pipette or pipette, and the ultracentrifuge tube was put upside down on the filter paper for 5 min for thoroughly desorbing The liquid was resuspended by adding 0.5 ml PBS, transferred to a 1.5 ml centrifuge tube, and placed at −80° C. and preserved for research.

(25) The exosomes were lysed by nanosight or exosome lysate for 30 minutes, and then the concentration was determined by BCA kit, and the morphology was observed by electron microscopy to confirm the isolation of tumor exosomes.

(26) The results of the test: the particle diameter, density and other parameters detected by nanosight are consistent with the characteristics of the exosomes, and the particle size observed by electron microscopy is also consistent with the size of the exosomes. The isolated exosomes are obtained (FIG. 4).

(27) Further, the exosome-specific markers CD63 and TSG101 were detected by immunocolloidal gold electron microscopy. It was confirmed that these markers were present on the surface of the particles, and the exosomes were separated again (FIG. 5).

(28) Second, the expression of TβRII on exosomes was detected by flow cytometry.

(29) APC-TβRII direct-labeled primary antibody was added to the isolated exosomes in a ratio of 1:100, incubated for 30 minutes at room temperature in the dark, and washed three times with PBS.

(30) The treated sample was tested for the content of TβRII in its exosomes by flow cytometry.

(31) Test results: The content of TβRII in exosomes of breast cancer patients was higher than that in normal subjects (FIGS. 6, 7).

(32) Further analysis of the receiver's working curve showed that the peripheral blood exosome TβRII protein itself has a great advantage as a diagnostic marker for breast cancer, and its sensitivity and specificity are relatively high (FIG. 8).

(33) Further analysis of TβRII protein content in peripheral blood exosomes of patients with breast cancer before and after surgery showed that the content of TβRII protein in peripheral blood exosomes of patients with breast cancer decreased significantly (FIG. 9) and detection by immunocolloid gold electron microscopy. The content of TβRII protein in exosomes of patients with breast cancer before and after surgery showed that the content of TβRII protein in peripheral blood exosomes of postoperative breast cancer patients also decreased significantly (FIG. 10). It indicates that the content of TβRII protein in peripheral blood exosomes can also be used as a test for postoperative rehabilitation of breast cancer patients.

(34) The present invention collects serum of healthy people and breast cancer patients, and detects the content of TβRII positive exosomes by flow cytometry. Comparing the content of TβRII positive exosomes in healthy people and breast cancer patients, the best cut-off value was obtained, and the sensitivity and specificity of serum TβRII positive exosomes in breast cancer diagnosis were evaluated.

(35) The serum levels of TβRII-positive exosomes in breast cancer patients were significantly higher than those in healthy people. It indicates the application prospect of detecting the content of TβRII positive exosomes in human serum in the diagnosis of breast cancer.