CN110456080A - C14orf37 autoantibody detection reagent is preparing the purposes in screening lung cancer kit - Google Patents
C14orf37 autoantibody detection reagent is preparing the purposes in screening lung cancer kit Download PDFInfo
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- CN110456080A CN110456080A CN201910894444.7A CN201910894444A CN110456080A CN 110456080 A CN110456080 A CN 110456080A CN 201910894444 A CN201910894444 A CN 201910894444A CN 110456080 A CN110456080 A CN 110456080A
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
- G01N33/57407—Specifically defined cancers
- G01N33/57423—Specifically defined cancers of lung
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
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- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
- G01N33/57484—Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumor, cancer, neoplasia, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides, metabolites
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- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
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- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6884—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids from lung
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Abstract
The present invention relates to external diagnosis reagent fields, and in particular to C14orf37 autoantibody detection reagent is preparing the purposes in screening lung cancer kit.Present invention firstly discovers that the autoantibody of C14orf37 albumen is substantially less than healthy patients in Serum of Patients with Lung Cancer.The reagent that the present invention will test C14orf37 albumen autoantibody is used to prepare screening lung cancer kit, can be realized effective screening of lung cancer.
Description
Technical field
The present invention relates to external diagnosis reagent fields, and in particular to C14orf37 autoantibody detection reagent is in preparation lung cancer
Purposes in kit for screening.
Background technique
Lung cancer is that one of most common malignant tumour, morbidity and mortality are in rise year by year trend in the world, at present
Disease incidence occupies first place in the world, and seriously threatens human health and life.
Lung cancer is a kind of disease for being good at concealment, often develops to advanced stage in disease and just shows clinical symptoms, 70~
80% patients with lung cancer has been middle and advanced stage when being diagnosed to be with Lung Cancer Symptoms, and cancer cell has been spread, and misses best healing
Opportunity, five year survival rate are low.For the patients with lung cancer of early stage, giving birth to for 5 years or more for patient is greatly improved by treating in time
Deposit rate and life quality.Therefore the early diagnosis and the effective screening of progress of lung cancer are most important.
The screening of lung cancer, referring to does not have the related indication crowd of lung cancer to carry out routine physical examination those, before there is symptom
Discovery lung cancer in time.If the lung cancer molecular marker inside blood plasma can be found, for prompting clinician's early stage to patient
Relevant remedy measures or decision are taken to have great importance.
Autoantibody refers to the antibody that body generates itself organ, cell or cell component.Currently, certain albumen from
Body antibody has become the marker of lung cancer, such as: p53, NY-ESO-1, CYFRA (Tang Z-M, Ling Z-G, Wang
C-M,Wu Y-B,Kong J-L(2017)Serum tumor-associated autoantibodies as diagnostic
biomarkers for lung cancer:A systematic review and meta-analysis.PLoS ONE 12
(7):e0182117)。
C14orf37 (gene order number is Ensembl:ENSG00000139971), wide expression is in kidney (RPKM
5.3), in brain (RPKM 4.3) and other 15 kinds tissues.The relevant report of C14orf37 albumen autoantibody is had not yet to see,
Have no its prior art relevant to lung cancer.
Summary of the invention
The purpose of the present invention is to provide the detections of the lung cancer marker and the marker of a kind of new autoantibody class
Reagent is preparing the purposes in screening lung cancer kit.
Technical solution of the present invention includes:
The reagent of detection C14orf37 albumen autoantibody is preparing the purposes in screening lung cancer kit.
Purposes as the aforementioned, the reagent of the detection C14orf37 albumen autoantibody are enzyme-linked immunosorbent assay examination
Agent or linked immune analysis reagent.
The reagent of purposes as the aforementioned, the detection C14orf37 albumen autoantibody is western blot reagent.
Purposes as the aforementioned, the reagent of the detection C14orf37 albumen autoantibody are the examination of protein chip detection method
Agent.
Purposes as the aforementioned, the reagent of the detection C14orf37 albumen autoantibody are C14ORF37 in detection human serum
The reagent of albumen autoantibody.
A kind of screening lung cancer kit, it includes the reagent for detecting CC14orf37 albumen autoantibody.
The reagent of kit as the aforementioned, the detection C C14orf37 albumen autoantibody is enzyme-linked immunosorbent assay
With reagent or ELISA reagent.
The reagent of kit as the aforementioned, the detection C14orf37 albumen autoantibody is western blot reagent.
Kit as the aforementioned, the reagent of the detection C14orf37 albumen autoantibody are protein chip detection method use
Reagent.
Kit as the aforementioned, the reagent of the detection C14orf37 albumen autoantibody are in detection human serum
The reagent of C14orf37 albumen autoantibody.
It is of the invention it is critical that the content of C14orf37 autoantibody and the risk for suffering from lung cancer in blood of human body has been determined
Significant correlation, therefore the risk for suffering from lung cancer can be judged by the content of C14orf37 autoantibody in detection blood of human body,
, can be using various means disclosed in the prior art as C14orf37 autoantibody means in specific detection blood of human body, this
Inventive embodiments specifically use enzyme-linked immune analytic method (protein chip) to be detected, but are not limited only to the means, any
The method for being able to detect C14orf37 autoantibody content is used equally for screening lung cancer.
The present invention provides a kind of new screening lung cancer markers and a kind of new screening lung cancer kit, can be realized lung
Effective screening of cancer;And patient can be injured very low using serum as test sample.The present invention has good application prospect.
Obviously, above content according to the present invention is not being departed from according to the ordinary technical knowledge and customary means of this field
Under the premise of the above-mentioned basic fundamental thought of the present invention, the modification, replacement or change of other diversified forms can also be made.
Above content of the invention is described in further detail again below by way of specific embodiment.But it should not be by this
The range for being interpreted as the above-mentioned theme of the present invention is only limitted to example below.All technologies realized based on above content of the present invention are equal
Belong to the scope of the present invention.
Hereinafter " C14orf37 autoantibody " refers to " C14orf37 albumen autoantibody ".
Detailed description of the invention
Fig. 1: C14orf37 autoantibody comparison in patients with lung cancer (LC), normal healthy controls (NC) serum slurry.
Fig. 2: patients with lung cancer (LC) and normal healthy controls (NC) ROC are analyzed.
Specific embodiment
The relationship of C14orf37 autoantibody and lung cancer in 1 blood plasma of embodiment
One, clinical data
Patients with lung cancer 30 are chosen, normal healthy controls 30, essential information is as follows:
Essential information | Patients with lung cancer | Normal healthy controls |
Number | 30 | 30 |
Age | 58±10.5 | 42±8.9 |
Masculinity proportion | 20 (66.7%) | 13 (46.7%) |
Two, testing principle
HuProtTMC14orf37 albumen is fixed on human protein's custom chip, and (used C14orf37 albumen is
Full-length proteins, protein sequence number are Ensembl:ENSP00000477692), after increase serum is incubated for, C14orf37 itself in serum
Antibody (including mainly IgG, IgM type antibody, there are also other types of antibody) can be in conjunction with up, and cleaning removes unbonded
Antibody and other oroteins, then with anti-human IgM fluorescent marker secondary antibody (cy5 mark, present red) and anti-human igg fluorescence secondary antibody
(cy3 label, green is presented) detection reads signal, the power and the affinity and quantity of antibody of signal by Fluorescence Scanner
It is positively correlated.
Three, method
Reagent used in this part is as follows:
1) rewarming: chip is taken out from -80 DEG C of refrigerators, 4 DEG C of refrigerator rewarming half an hour is placed in, is subsequently placed in room temperature rewarming
15min;
2) close: the chip after rewarming fixes 14 blocks fences, and after fixing, envelope is added into each block
Liquid is closed, and is placed on side-sway shaking table, room temperature closes 3hr;
3) serum sample is incubated for: after the completion of closing, then confining liquid to the greatest extent is rapidly added preprepared serum and is incubated for
Liquid, every chip can be incubated for 14 serum samples, and the loading volume of each serum sample is 200 μ L, side-sway shaking table 20rpm, and 4 DEG C
It is incubated overnight (serum sample is firstly placed on 4 DEG C of chromatography cabinet freeze thawing, adds Incubating Solution with 1:50 dilution proportion, obtains serum Incubating Solution);
4) it cleans: chip and chip fence being taken out together, suck sample, is then rapidly added isometric PBST, such as
This circulation for several times, guarantees when removing chip fence no cross contamination between serum sample.After removing chip fence, chip is placed in
Added with the chip cleaning box of cleaning solution, horizontal shaker, room temperature 80rpm is cleaned 3 times, each 10min;
5) secondary antibody is incubated for: chip being transferred in the incubation box that joined 3mL secondary antibody Incubating Solution, side-sway shaking table 40rpm is kept away
Light, room temperature 1hr;
6) it cleans: chip being taken out into (upper surface for paying attention to touch or scratching chip), is placed in the core added with cleaning solution
Piece cleaning box, horizontal shaker, room temperature 80rpm are cleaned 3 times, each 10min.It is cleaned 2 times with ddH2O after the completion, each 10min;
7) dry;
8) it scans: being scanned using brilliant core LuxScan 10K micro-array chip scanner;
9) data are extracted: corresponding GAL file (having recorded albumen position in chip) is opened, by chip image and
The each array of GAL file is integrally aligned, and presses automatic aligning button, is extracted data and is saved.
Four, result
The Average expression level of C14orf37 autoantibody in Plasma of The Patients With Lung Cancer is that (fluorescence signal is opposite by 132.7SNR
Quantitative ratio), the Average expression level of C14orf37 autoantibody is 231.7SNR in normal healthy controls blood plasma.Lung cancer group and health
Control group (p < 0.05) compares statistically significant (Fig. 1).The ROC of lung cancer group and normal healthy controls analyzes result specificity
93.1%, sensibility is 37.9% (Fig. 2), shows that C14orf37 autoantibody can specifically distinguish lung cancer and normal healthy controls.
It can be seen from the above result that the level difference of patients with lung cancer and C14orf37 autoantibody in the serum of non-lung cancer patient
Significantly, by the level of C14orf37 autoantibody in detection serum, it can achieve the purpose that screening lung cancer.
The composition and its application method of the detection kit of the invention of embodiment 2
One, kit forms
Detection kit (14 person-portion):
Two, kit application method
With 1 Part III of embodiment --- " detection of C14orf37 autoantibody in serum ".
Kit of the invention can be by the level of C14orf37 autoantibody in detection serum, can be with screening people to be checked
Group suffers from the risk of lung cancer: if C14orf37 autoantibody is low (for Healthy People), the risk for suffering from lung cancer is high, if
C14orf37 autoantibody is high, then the risk for suffering from lung cancer is low.It can be used for the auxiliary diagnosis of clinical lung cancer, take phase for patient
The remedy measures or decision of pass provide effective foundation, and potential applicability in clinical practice is good.
Claims (10)
1. the reagent of detection C14orf37 albumen autoantibody is preparing the purposes in screening lung cancer kit.
2. purposes as described in claim 1, which is characterized in that the reagent of the detection C14orf37 albumen autoantibody is enzyme
Linked immunosorbent adsorption test reagent or linked immune analysis reagent.
3. purposes as described in claim 1, which is characterized in that it is described detection C14orf37 albumen autoantibody reagent be
Western blot reagent.
4. purposes as described in claim 1, which is characterized in that the reagent of the detection C14orf37 albumen autoantibody is egg
White chip detecting method reagent.
5. the purposes as described in Claims 1 to 4 is any, which is characterized in that the detection C14orf37 albumen autoantibody
Reagent is the reagent for detecting C14orf37 albumen autoantibody in human serum.
6. a kind of screening lung cancer kit, which is characterized in that it includes the reagent for detecting C14orf37 albumen autoantibody.
7. kit as claimed in claim 6, which is characterized in that it is described detection C14orf37 albumen autoantibody reagent be
Enzyme-linked immunosorbent assay reagent or ELISA reagent.
8. kit as claimed in claim 6, which is characterized in that it is described detection C14orf37 albumen autoantibody reagent be
Western blot reagent.
9. kit as claimed in claim 6, which is characterized in that it is described detection C14orf37 albumen autoantibody reagent be
Protein chip detection method reagent.
10. the kit as described in claim 5~9 is any, which is characterized in that the detection C14orf37 albumen autoantibody
Reagent be detect human serum in C14orf37 albumen autoantibody reagent.
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Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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US20090047689A1 (en) * | 2007-06-20 | 2009-02-19 | John Kolman | Autoantigen biomarkers for early diagnosis of lung adenocarcinoma |
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Publication number | Priority date | Publication date | Assignee | Title |
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US20090047689A1 (en) * | 2007-06-20 | 2009-02-19 | John Kolman | Autoantigen biomarkers for early diagnosis of lung adenocarcinoma |
Non-Patent Citations (1)
Title |
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K.K.杰恩: "《生物标志物手册》", 31 May 2015 * |
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