Methods for diagnosing and evaluating cancer

Abstract

Methods for diagnosing cancer, such as prostate, ovarian or breast cancer, as well as leukemia, are provided. Such methods may employ binding agents, such as antibodies or CAR sequences of OB-cadherin or N-cadherin, that specifically bind to OB-cadherin or N-cadherin, or polynucleotides that hybridize to a polynucleotide encoding OB-cadherin or N-cadherin. Also provided are methods for monitoring the progression of a cancer and to evaluate the metastatic potential of a cancer.

1 .- 43 . (Canceled).  
     
     
         44 . A method for determining the presence or absence of a cancer in a patient, comprising the steps of: 
 (a) contacting a biological sample obtained from a patient with a binding agent that specifically binds to N-cadherin; and    (b) detecting in the sample an amount of polypeptide that binds to the binding agent, relative to a predetermined cut-off value, and therefrom determining the presence or absence of a cancer in the patient.    
     
     
         45 . A method according to  claim 44  wherein the binding agent is a monoclonal antibody.  
     
     
         46 . A method according to  claim 44 , wherein the binding agent comprises a N-cadherin CAR sequence, or an analogue or mimetic thereof.  
     
     
         47 . A method according to  claim 44 , wherein the cancer is selected from the group consisting of leukemia, prostate cancer, breast cancer and ovarian cancer.  
     
     
         48 . A method according to  claim 44 , wherein the binding agent specifically binds to an extracellular domain of N-cadherin.  
     
     
         49 . A method according to  claim 44 , wherein the biological sample is selected from the group consisting of blood, serum, urine, tumor biopsies, peritoneal fluid, cerebrospinal fluid, prostate secretions and fractions of the foregoing samples.  
     
     
         50 . A method for monitoring the progression of a cancer in a patient, comprising the steps of: 
 (a) contacting a biological sample obtained from a cancer patient at a first point in time with a binding agent that specifically binds to N-cadherin;    (b) detecting in the sample an amount of polypeptide that binds to the binding agent;    (c) repeating steps (a) and (b) using a biological sample obtained from the patient at a subsequent point in time; and    (d) comparing the amount of polypeptide detected in step (c) to the amount detected in step (b) and therefrom monitoring the progression of the cancer in the patient.    
     
     
         51 . A method according to  claim 50  wherein the binding agent is a monoclonal antibody.  
     
     
         52 . A method according to  claim 50 , wherein the binding agent comprises a N-cadherin CAR sequence, or an analogue or mimetic thereof.  
     
     
         53 . A method according to  claim 50 , wherein the cancer is selected from the group consisting of leukemia, prostate cancer, breast cancer and ovarian cancer.  
     
     
         54 . A method according to  claim 50 , wherein the binding agent specifically binds to an extracellular domain of N-cadherin.  
     
     
         55 . A method according to  claim 50 , wherein the biological sample is selected from the group consisting of blood, serum, urine, tumor biopsies, peritoneal fluid, prostate secretions and fractions of the foregoing samples.  
     
     
         56 . A method for evaluating the metastatic potential of a cancer in a patient, comprising the steps of: 
 (a) contacting a biological sample obtained from a cancer patient afflicted with cancer with a binding agent that specifically binds to N-cadherin; and    (b) detecting in the sample an amount of polypeptide that binds to the binding agent, relative to a predetermined cut-off value, and therefrom evaluating the metastatic potential of the cancer in the patient.    
     
     
         57 . A method according to  claim 56  wherein the binding agent is a monoclonal antibody.  
     
     
         58 . A method according to  claim 56 , wherein the binding agent comprises a N-cadherin CAR sequence, or an analogue or mimetic thereof.  
     
     
         59 . A method according to  claim 56 , wherein the cancer is selected from the group consisting of leukemia, prostate cancer, breast cancer and ovarian cancer.  
     
     
         60 . A method according to  claim 56 , wherein the binding agent specifically binds to an extracellular domain of N-cadherin.  
     
     
         61 . A method according to  claim 56 , wherein the biological sample is selected from the group consisting of blood, serum, urine, tumor biopsies, peritoneal fluid, prostate secretions and fractions of the foregoing samples.  
     
     
         62 . A method for determining the presence or absence of a metastatic cancer in a patient, comprising the steps of: 
 (a) contacting a biological sample obtained from a patient with an oligonucleotide that hybridizes to a polynucleotide that encodes N-cadherin; and    (b) detecting in the sample an amount of a polynucleotide that hybridizes to the oligonucleotide, relative to a predetermined cut-off value, and therefrom determining the presence or absence of a metastatic cancer in the patient.    
     
     
         63 . A method according to  claim 62 , wherein the amount of polynucleotide that hybridizes to the oligonucleotide is determined using polymerase chain reaction.  
     
     
         64 . A method according to  claim 62 , wherein the amount of polynucleotide that hybridizes to the oligonucleotide is determined using a hybridization assay.  
     
     
         65 . A method according to  claim 62 , wherein the cancer is selected from the group consisting of leukemia, prostate cancer, breast cancer and ovarian cancer.  
     
     
         66 . A method according to  claim 62 , wherein the biological sample is an RNA or cDNA preparation.  
     
     
         67 . A method for monitoring progression of a cancer in a patient, comprising the steps of: 
 (a) contacting a biological sample obtained from a cancer patient with an oligonucleotide that hybridizes to a polynucleotide that encodes N-cadherin;    (b) detecting in the sample an amount of a polynucleotide that hybridizes to the oligonucleotide;    (c) repeating steps (a) and (b) using a biological sample obtained from the patient at a subsequent point in time; and    (d) comparing the amount of polynucleotide detected in step (c) with the amount detected in step (b) and therefrom monitoring progression of a cancer in the patient.    
     
     
         68 . A method according to  claim 67 , wherein the amount of polynucleotide that hybridizes to the oligonucleotide is determined using polymerase chain reaction.  
     
     
         69 . A method according to  claim 67 , wherein the amount of polynucleotide that hybridizes to the oligonucleotide is determined using a hybridization assay.  
     
     
         70 . A method according to  claim 67 , wherein the cancer is selected from the group consisting of leukemia, prostate cancer, breast cancer and ovarian cancer.  
     
     
         71 . A method according to  claim 67 , wherein the biological sample is an RNA or cDNA preparation.  
     
     
         72 . A method for evaluating the metastatic potential of a cancer in a patient, comprising the steps of: 
 (a) contacting a biological sample obtained from a cancer patient with an oligonucleotide that hybridizes to a polynucleotide that encodes N-cadherin; and    (b) detecting in the sample an amount of a polynucleotide that hybridizes to the oligonucleotide, relative to a predetermined cut-off value, and therefrom evaluating the metastatic potential of the cancer in the patient.    
     
     
         73 . A method according to  claim 72 , wherein the amount of polynucleotide that hybridizes to the oligonucleotide is determined using polymerase chain reaction.  
     
     
         74 . A method according to  claim 72 , wherein the amount of polynucleotide that hybridizes to the oligonucleotide is determined using a hybridization assay.  
     
     
         75 . A method according to  claim 72 , wherein the cancer is selected from the group consisting of leukemia, prostate cancer, breast cancer and ovarian cancer.  
     
     
         76 . A method according to  claim 72 , wherein the biological sample is an RNA or cDNA preparation.