US2021145700A1PendingUtilityA1
Genetic products differentially expressed in tumors and the use thereof
Est. expiryMay 18, 2024(expired)· nominal 20-yr term from priority
G01N 33/57595C07K 16/44C07K 16/18A61K 49/00C07K 16/30C07K 14/705C07K 2317/34A61P 35/00A61P 43/00C07K 16/28A61K 2039/505C07K 14/47C07K 16/303C12N 9/88C07K 2317/24A61K 47/6851A61K 6/00C12Y 406/01002A61P 35/04C07K 16/3046C07K 2317/73C07K 16/3076C07K 2317/75G01N 33/57496
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Claims
Abstract
According to the invention, gene products expressed in a tumor-associated manner and the nucleic acids coding therefor were identified. The invention relates to the therapy and diagnosis of diseases wherein said gene products expressed in a tumor-associated manner are aberrantly expressed. The invention also relates to proteins, polypeptides and peptides which are expressed in a tumor associated manner and to nucleic acids coding therefor.
Claims
exact text as granted — not AI-modified1 - 101 . (canceled)
102 . A method for detecting a tumor-associated antigen, the method comprising the steps of:
(a) providing a biological sample from a patient, wherein the biological sample is suspected of containing cancerous cells or cancerous tissue; and (b) determining a glycosylation pattern of claudin-18A2 protein contained within the biological sample, wherein presence of a non-glycosylated form of claudin-18A2 is indicative of the biological sample containing cancerous cells or cancerous tissue.
103 . The method of claim 102 , wherein the non-glycosylated form of claudin-18A2 comprises a non-glycosylated residue at position 37, 38, 45, 116, 141, 146, or 205 of SEQ ID NO: 16.
104 . A method for selecting and administering a cancer therapy to a patient in need thereof, the method comprising the steps of:
(a) providing a biological sample from the patient, wherein the biological sample comprises cancerous tissue or tissue suspected of being cancerous; (b) detecting within the biological sample a non-glycosylated form of claudin-18A2 protein; and (c) administering to the patient a therapeutic agent that selectively binds to the non-glycosylated form of claudin-18A2 protein.
105 . The method of claim 104 , wherein the patient has been diagnosed with pancreatic cancer or gastric cancer.
106 . The method of claim 105 , wherein the pancreatic cancer comprises pancreatic adenocarcinoma.
107 . The method of claim 105 , wherein the gastric cancer comprises gastric adenocarcinoma.
108 . The method of claim 104 , wherein the non-glycosylated form of claudin-18A2 protein comprises a non-glycosylated residue at position 37, 38, 45, 116, 141, 146, or 205 of SEQ ID NO: 16.
109 . The method of claim 108 , wherein the patient has been diagnosed with pancreatic cancer or gastric cancer.
110 . The method of claim 109 , wherein the pancreatic cancer comprises pancreatic adenocarcinoma.
111 . The method of claim 109 , wherein the gastric cancer comprises gastric adenocarcinoma.
112 . The method of claim 108 , wherein the therapeutic agent is a therapeutic antibody or antigen binding fragment thereof.
113 . The method of claim 112 , wherein the therapeutic antibody is selected from the group consisting of a chimeric antibody, a humanized antibody, and an immunoreactive fragment of any of the foregoing.
114 . The method of claim 112 , wherein the therapeutic antibody is coupled to an additional therapeutic agent.
115 . The method of claim 114 , wherein the additional therapeutic agent is an anticancer agent, a toxin, a radioactive compound or a cytostatic or cytolytic compound.
116 . A method for treating a cancer patient, the method comprising:
administering an anti-claudin-18A2 antibody to the patient, wherein a biological sample obtained from the patient comprises a non-glycosylated form of claudin-18A2 protein.
117 . The method of claim 116 , wherein the non-glycosylated form of claudin-18A2 protein comprises a non-glycosylated residue at position 37, 38, 45, 116, 141, 146, or 205 of SEQ ID NO: 16.
118 . The method of claim 116 , wherein the cancer is pancreatic cancer or gastric cancer.
119 . The method of claim 118 , wherein the pancreatic cancer comprises pancreatic adenocarcinoma.
120 . The method of claim 118 , wherein the gastric cancer comprises gastric adenocarcinoma.
121 . The method of claim 116 , wherein the therapeutic antibody is selected from the group consisting of a chimeric antibody, a humanized antibody, and an immunoreactive fragment of any of the foregoing.Join the waitlist — get patent alerts
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