Methods, assays and kits for cancer diagnosis and screening utilizing glycan-binding and glycan epitopes
OwnerMarko Vuskovic, Margaret Huflejtinventors
Life of this patent
Estimating the term…
Loading patent…
OwnerMarko Vuskovic, Margaret Huflejtinventors
Estimating the term…
The invention relates to the diagnosis, monitoring, prognosis, and/or prediction of cancer utilizing the detection or measurement of glycan-protein interactions, particularly glycan-antibody interactions. The invention relates to carbohydrate-containing molecules that are utilized in bioanalytical systems, methods and kits for detecting neoplasia and methods related thereto and based thereon. In an exemplary embodiment glycans or glycopolymers are carried in an array, on beads or in a microfluidic system for diagnostic screening for risk of neoplasia, the existence of neoplasia in a patient, or for treatment monitoring. In such an embodiment, the bioanalytic system identifies binding interactions between molecules in a patient test sample (e.g., glycan compositions) and the glycans or glycopolymers. The glycan-binding compositions may be used to generate an immune response against cancer cell epitopes. Alternatively, antibody therapeutics can be developed that are useful for binding to glycan compositions on a cell surface.
A method of detecting or monitoring lung cancer in a patient comprising measuring at least one antiglycan binding profile of a test sample from said patient and comparing the measured profile with a profile of normal patient or profile of a patient with a history of smoking, wherein a substantial difference in the test sample profile versus the normal or history of smoking profiles is indicative of lung cancer.
A method for diagnosing a patient for lung cancer or risk of lung cancer comprising obtaining a test sample from a patient and detecting the presence of antiglycan autoantibodies:
A method for detecting, diagnosing or monitoring breast cancer in a patient comprising obtaining a test sample from a patient and detecting the presence of antiglycan antibodies:
A method for facilitating the diagnosis of IDC in a patient comprising obtaining a test sample from a patient and detecting the presence of antiglycan autoantibodies against at least one of the glycans listed in Table 10.
A method for detecting, diagnosing or monitoring ovarian cancer in a patient comprising obtaining a test sample from a patient and detecting the presence of antiglycan autoantibodies against at least one of the glycans listed in Table 12.
A method for diagnosis or monitoring of cancer in a patient comprising:
A method of detecting or monitoring cancer in a patient comprising measuring at least one antiglycan binding profile of a test sample from said patient and comparing the measured profile with a profile of normal patient or profile of a patient with a family history of cancer, wherein a substantial difference in the test sample profile versus the normal or history of cancer is indicative of cancer.
A kit for diagnosing or monitoring cancer in an individual wherein the antiglycan binding profile of a test sample from said individual is determined and comparing the measured profile with a profile of normal patient or profile of a patient with a family history of cancer, wherein said kit comprises an array of glycan molecules selected from the glycans set out in Tables 6, 8, 10 and 12.
A kit for diagnosing or monitoring lung cancer in an individual wherein the antiglycan binding profile of a test sample from said individual is determined and comparing the measured profile with a profile of normal patient or profile of a patient with a family history of cancer or a smoker, wherein said kit comprises:
A kit for diagnosing or monitoring breast cancer in an individual wherein the antiglycan binding profile of a test sample from said individual is determined and comparing the measured profile with a profile of normal patient or profile of a patient with a family history of cancer or a smoker, wherein said kit comprises:
A kit for diagnosing or monitoring ovarian cancer in an individual wherein the antiglycan binding profile of a test sample from said individual is determined and comparing the measured profile with a profile of normal patient or profile of a patient with a family history of cancer, wherein said kit comprises:
A method of detecting or monitoring mesothelioma in a patient comprising measuring at least one antiglycan binding profile of a test sample from said patient and comparing the measured profile with a profile of normal patient or profile of a patient exposed to asbestos, wherein a substantial difference in the test sample profile versus the normal or asbestos exposed profiles is indicative of mesothelioma.
A kit for diagnosing or monitoring mesothelioma in an individual wherein the antiglycan binding profile of a test sample from said individual is determined and comparing the measured profile with a profile of normal patient or profile of a patient exposed to asbestos, wherein said kit comprises one or more glycan molecules selected from the glycans set out in Table 15.
Dependencies are inferred from the claim text.