US2016158316A1PendingUtilityA1
Drg11-responsive (dragon) gene family
Est. expiryApr 18, 2022(expired)· nominal 20-yr term from priority
A61P 43/00A61P 37/00A61P 9/00A61P 35/00A61P 25/00C07K 14/461A61K 38/00C12Q 1/6886C12Q 2600/158C07K 16/18A01K 2217/075C12Q 2600/156C07K 2317/92C07K 14/47A61K 38/179C07K 14/43509A01K 2217/05C12Q 2600/112A61P 19/00G01N 2333/71A61P 21/00A61P 17/00G01N 33/5758G01N 33/57484
64
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Claims
Abstract
This invention features methods and compositions useful for treating and diagnosing diseases of the nervous system, retina, skin, muscle, joint, and cartilage using a Dragon family protein. Protein and nucleic acid sequences of human, murine, zebrafish, and C. elegans Dragon family members are also disclosed.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 - 53 . (canceled)
54 . A method of treating a DRG11-Responsive Axonal Guidance and Outgrowth of Neurite (DRAGON)-related cancer in a subject in need thereof, said method comprising administering to said subject a therapeutically effective amount of a DRAGON protein.
55 . The method of claim 54 , wherein the DRAGON-related cancer is selected from the group consisting of a glioma, a Schwanoma, and a neurofibromatosis.
56 . The method of claim 54 , wherein the DRAGON protein is administered with a pharmaceutically acceptable carrier or salt.
57 . A method of diagnosing a subject as having, or having an increased risk of developing, a DRAGON-related cancer, the method comprising taking a biological sample from the subject and assessing whether the sample contains a mutated DRAGON nucleic acid, wherein the mutated DRAGON nucleic acid encodes a mutated DRAGON protein, wherein the mutated DRAGON protein exhibits increased biological activity relative to a wild-type DRAGON protein, wherein if the sample contains the mutated DRAGON nucleic acid, the subject has or is at risk of having a DRAGON-related cancer.
58 . The method of claim 57 , wherein assessing comprises polymerase chain reaction (PCR) analysis.
59 . The method of claim 57 , wherein assessing comprises restriction fragment length polymorphism (RFLP) analysis.
60 . The method of claim 57 , wherein the DRAGON-related cancer is selected from the group consisting of a glioma, a Schwanoma, and a neurofibromatosis.
61 . The method of claim 57 , wherein the sample is a blood sample or a tissue biopsy.
62 . The method of claim 57 , wherein the subject is human.
63 . A method of diagnosing a subject as having, or having an increased risk of developing, a DRAGON-related cancer, the method comprising taking a biological sample from the subject; determining the expression level of a DRAGON nucleic acid and/or protein; comparing the expression level of the DRAGON nucleic acid and/or protein to a control sample; and determining whether the subject has, or has an increased risk of developing a DRAGON-related cancer based on the comparison.
64 . The method of claim 63 , wherein the expression level of the DRAGON nucleic acid and/or protein is higher than the control sample, the subject has, or has an increased risk of developing a DRAGON-related cancer.
65 . The method of claim 63 , wherein determining the expression level of a nucleic acid comprises Northern blot analysis.
66 . The method of claim 63 , wherein determining the expression level of a nucleic acid comprises PCR analysis.
67 . The method of claim 10 , wherein determining the expression level of a protein comprises enzyme-linked immunosorbent assay (ELISA) analysis.
68 . The method of claim 63 , wherein determining the expression level of a protein comprises Western blot analysis.
69 . The method of claim 63 , wherein determining the expression level of a protein comprises radioimmunoassay (RIA) analysis.Join the waitlist — get patent alerts
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