Collagen-binding synthetic peptidoglycans, preparation, and methods of use
US-9512192-B2 · Dec 6, 2016 · US
US9796761B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9796761-B2 |
| Application number | US-201013384031-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 12, 2010 |
| Priority date | Jul 14, 2009 |
| Publication date | Oct 24, 2017 |
| Grant date | Oct 24, 2017 |
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The present invention is directed to developing a glycan markers capable of detecting a hepatic disease, and more specifically to developing a glycan marker indicating a hepatic disease-state. Furthermore, the present invention is also directed to developing a glycan marker capable of distinguishing hepatic disease-states with the progress of hepatocarcinoma. The present inventors identified, among the serum glycoproteins, glycopeptides and glycoproteins in which a glycan structure specifically changes due to a hepatic diseases including hepatocarcinoma and provide these as novel glycan markers (glycopeptide and glycoprotein) specific to hepatic disease-states.
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The invention claimed is: 1. A method for detecting hepatocarcinoma in a subject, comprising analyzing a glycosylation change associated with the progress of hepatocarcinoma in at least one hepatic disease-state-indicating glycan marker glycoprotein in a specimen taken from the subject, wherein the hepatic disease-state-indicating glycan marker glycoprotein is protein CSF1R having a glycosylation change including fucosylation; wherein the analyzing comprises measurement of an amount of the hepatic disease-state-indicating glycan marker glycoprotein in combination with measurement of LCA binding the hepatic disease-state-indicating glycan marker glycoprotein or AAL binding the hepatic disease-state-indicating glycan marker glycoprotein, wherein elevated hepatic disease-state-indicating glycan marker glycoprotein in combination with elevated LCA binding the hepatic disease-state-indicating glycan marker glycoprotein or AAL binding the hepatic disease-state-indicating glycan marker glycoprotein is indicative of hepatocarcinoma in the subject, provided that the hepatocarcinoma is not one arisen from metastasis. 2. A method for detecting hepatocarcinoma in a subject, comprising analyzing a glycosylation change associated with the progress of hepatocarcinoma in CSF1R in a specimen taken from the subject, wherein the analyzing comprises measurement of an amount of CSF1R binding to a lectin selected from a group consisting of AOL, AAL, ECA, ABA and WFA, wherein increased CSF1R binding to a lectin selected from a group consisting of AOL, AAL, ECA, ABA and WFA is indicative of hepatocarcinoma in the subject. 3. A method for determining progress of fibrosis in a subject, comprising analyzing a glycosylation change associated with the progress of fibrosis in CSF1R in a specimen taken from the subject, wherein the analyzing comprises measurement of an amount of CSF1R binding to LCA or AAL in the specimen taken from the subject and in a specimen from a healthy subject, and comparing the amount of CSF1R binding to LCA or AAL in the specimen from the subject and the specimen from the healthy subject, wherein increased CSF1R binding to LCA or AAL in the specimen taken from the subject is indicative of progress of fibrosis in the subject. 4. A method for determining progress of fibrosis, detecting hepatic cirrhosis, or predicting incidence and recurrence of hepatocarcinoma in a subject comprising analyzing a glycosylation change associated with the progress of fibrosis, hepatic cirrhosis, or hepatocarcinoma in CSF1 R in a specimen taken from the subject, wherein the analyzing comprises measurement of an amount of CSF1 R binding to WFA in the specimen taken from the subject and in a specimen from a healthy subject, and comparing the amount of CSF1 R binding to WFA in the specimen from the subject and the specimen from the healthy subject, wherein increased CSF1 R binding to WFA in the specimen taken from the subject is indicative of progress of fibrosis, hepatic cirrhosis, or predicting incidence and recurrence of hepatocarcinoma in the subject. 5. A method for detecting hepatocarcinoma in a subject, comprising analyzing a glycosylation change associated with the progress of hepatocarcinoma in at least one hepatic disease-state-indicating glycan marker glycoprotein in a specimen taken from the subject, wherein the hepatic disease-state-indicating glycan marker glycoprotein is protein CSF1R having a glycosylation change including fucosylation; wherein the analyzing comprises measurement of an amount of the hepatic disease-state-indicating glycan marker glycoprotein in the specimen taken from the subject in combination with measurement of LCA binding the hepatic disease-state-indicating glycan marker glycoprotein or AAL binding the hepatic disease-state-indicating glycan marker glycoprotein in the specimen taken from the subject wherein an elevated amount of the hepatic disease-state-indicating glycan marker glycoprotein in the specimen taken from the subject in combination with elevated LCA binding the hepatic disease-state-indicating glycan marker glycoprotein or AAL binding the hepatic disease-state-indicating glycan marker glycoprotein in the specimen taken from the subject is indicative of hepatocarcinoma in the subject.
of the liver or pancreas · CPC title
involving tumour-associated glycolinkage [TAG] · CPC title
Liver diseases, e.g. portal hypertension, fibrosis, cirrhosis, bilirubin · CPC title
involving antibodies to sugar part of glycoproteins · CPC title
from mammals · CPC title
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