US2010136581A1PendingUtilityA1
Diagnosis and treatment of malignant neoplasms
Est. expiryNov 8, 2019(expired)· nominal 20-yr term from priority
C12N 2799/027C12N 9/0071C12N 2310/315C12Q 1/26C12Y 114/11016C07K 16/40C07K 14/47C12N 15/1137G01N 2500/00A61P 35/00A61P 43/00G01N 2500/10A61K 2039/505C12N 2310/111A61K 31/4412A61K 31/00G01N 33/5758G01N 33/575
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Claims
Abstract
The invention features a method for diagnosing a malignant neoplasm in a mammal by contacting a bodily fluid from the mammal with an antibody which binds to an human aspartyl (asparaginyl) beta-hydroxylase (HAAH) polypeptide and methods of treating malignant neoplasms by inhibiting HAAH.
Claims
exact text as granted — not AI-modified1 . A method for diagnosing a malignant neoplasm in a mammal, comprising contacting a bodily fluid from said mammal with an antibody or fragment thereof which binds to an human aspartyl (asparaginyl) beta-hydroxylase (HAAH) polypeptide under conditions sufficient to form an antigen-antibody complex and detecting the antigen-antibody complex, wherein an increase in antigen-antibody complex indicates an increase in HAAH level compared to a normal noncancerous control, said increase being indicative of a malignant neoplasm and wherein said antibody is a monoclonal antibody produced by hybridoma ATCC designation 3386.
2 . The method of claim 1 , wherein said neoplasm is derived from endodermal tissue.
3 . The method of claim 1 , wherein said neoplasm is selected from the group consisting of colon cancer, breast cancer, pancreatic cancer, liver cancer, and cancer of the bile ducts.
4 . The method of claim 1 , wherein said neoplasm is a cancer of the central nervous system (CNS).
5 . The method of claim 1 , wherein said bodily fluid is selected from the group consisting of a CNS-derived bodily fluid, blood, serum, urine, saliva, sputum, lung effusion, and ascites fluid.
6 . The method of claim 5 , wherein said bodily fluid is serum.
7 . The method of claim 1 , wherein the antigen-antibody complex is detected by a label selected from consisting of an enzymatic label, a fluorescent label, a chemiluminescent label, a radioactive label, and a dye label.
8 . The method of claim 1 , wherein said fragment of said monoclonal antibody is a single chain Fv molecule.
9 . The method of claim 1 , wherein said neoplasm is a hepatocellular carcinoma.
10 . The method of claim 1 , wherein said neoplasm is a cholangiocarcinoma.
11 . The method of claim 1 , wherein said neoplasm is a glioblastoma.
12 . The method of claim 1 , wherein said neoplasm is a neuroblastoma.
13 . The method of claim 1 , wherein said neoplasm is a pancreatic cancer.
14 . The method of claim 1 , wherein said tumor is a neuroectodermal tumor.
15 . The method of claim 1 , wherein said antibody comprises a first HAAH-specific antibody and a second HAAH-specific antibody.
16 . A method for prognosis of a malignant neoplasm of a mammal, comprising:
contacting a bodily fluid from said mammal with an antibody or fragment thereof which binds to an HAAH polypeptide under conditions sufficient to form an antigen-antibody complex and detecting the antigen-antibody complex; quantitating the amount of complex to determine the level of HAAH in said fluid; and comparing the level of HAAH in said fluid with a normal noncancerous control level of HAAH, wherein increasing levels of HAAH over time indicates an adverse prognosis, and wherein said antibody is a monoclonal antibody produced by hybridoma ATCC designation 3386.
17 . The method of claim 11 , wherein said fragment of said monoclonal antibody is a single chain Fv molecule.
18 . The method of claim 11 , wherein the antigen-antibody complex is detected by a label selected from consisting of an enzymatic label, a fluorescent label, a chemiluminescent label, a radioactive label, and a dye label.
19 . The method of claim 1 , wherein said neoplasm is a cancer of the central nervous system (CNS).
20 . A method for diagnosing a malignant neoplasm in a mammal, comprising contacting a bodily tissue from said mammal with an antibody or fragment thereof which binds to an human aspartyl (asparaginyl) beta-hydroxylase (HAAH) polypeptide under conditions sufficient to form an antigen-antibody complex and detecting the antigen-antibody complex, wherein an increase in antigen-antibody complex indicates an increase in HAAH level compared to a normal noncancerous control, said increase being indicative of a malignant neoplasm, wherein said antibody is a monoclonal antibody produced by hybridoma ATCC designation 3386, and wherein said fragment of said monoclonal antibody is a single chain Fv molecule.Cited by (0)
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