Identification of surface-associated antigens for tumor diagnosis and therapy
The invention relates to identifying tumor-associated genetic products and encoding nucleic acids thereof. A therapy and diagnosis of diseases in which the tumor-associated genetic products are aberrantly expressed, proteins, polypeptides and peptides which are expressed in association with tumor and the encoding nucleic acids for said proteins, polypeptides and peptides are also disclosed.
1. A method of diagnosing a cancer characterized by increased expression of a tumor-associated antigen, which method comprises detection of a nucleic acid which codes for the tumor-associated antigen in a biological sample isolated from a patient, said tumor-associated antigen encoded by the nucleic acid sequence of SEQ ID NO: 5;
wherein the detection comprises
(i) contacting nucleic acids isolated from the biological sample with a probe prepared by amplification with a primer set consisting of SEQ ID NO: 7 and SEQ ID NO: 8 under conditions that allow the probe to hybridize to the nucleic acid within the sequence of SEQ ID NO: 5, and
(ii) detecting a complex formed between the probe and the nucleic acids of SEQ ID NO: 5 from the biological sample;
wherein an increased amount of complex comprising the sequence of SEQ ID NO:5 in the biological sample as compared to a normal sample without cancer indicates the patient has cancer and;
wherein the cancer is selected from the group consisting of renal cancer, gastric cancer, pancreatic cancer, ear nose and throat (ENT) cancer, breast cancer, and lung cancer.
2. The method as claimed in claim 1 , in which the tumor-associated antigen comprises the amino acid sequence of SEQ ID NO: 6.
3. A method of diagnosing a cancer characterized by increased expression of a tumor-associated antigen, which method comprises detection of a nucleic acid which codes for the tumor-associated antigen in a biological sample isolated from a patient, said tumor-associated antigen encoded by the nucleic acid sequence of SEQ ID NO: 5,
wherein the detection comprises:
i) contacting nucleic acids isolated from the biological sample with a primer set consisting of SEQ ID NO: 7 and SEQ ID NO: 8, under conditions which amplifies the nucleic acids within the sequence of SEQ ID NO: 5 from the biological sample,
ii) detecting the amplified nucleic acids,
wherein an increased amount of amplified nucleic acids within the sequence of SEQ ID NO:5 in the biological sample as compared to a normal sample without cancer indicates the patient has cancer,
wherein the cancer is selected from the group consisting of renal cancer, gastric cancer, pancreatic cancer, ear nose and throat (ENT) cancer, breast cancer, and lung cancer.
4. The method as claimed in claim 3 , in which the tumor-associated antigen comprises the amino acid sequence of SEQ ID NO: 6.