Page 51 - Bio Engineering Approaches to Cancer Diagnosis and Treatment
P. 51

3.2 Monoclonal antibody-based immune assays       49




                  used for quantitation of CA215 in serum specimens of patients with cancer. RP215
                  has been used as the unique probe for cancer diagnosis.
                     A comparative research list of the positive rates of serum CA215 levels in dif-
                  ferent types of cancer including: lung (52%), colon (44%), ovary (59%), breast
                  (38%), pancreas (51%) esophagus (61%), stomach (60%), kidney (38%), and lym-
                  phoma (83%) [11]. Immunohistochemically tissue staining studies with RP215 as
                  the immune probe for cancerous antigen receptors also have indicated widespread
                  expressions  of  RP215-epitope  among  various  cancer  tissues.  Among  these,  the
                  results were: ovary (n = 87, 64.4%), cervix (n = 51, 84.3%), endometrium (n = 36,
                  77.8%), stomach (n = 93, 49.5%), colon (n = 87, 43.6%), esophagus (n = 56, 75.7%),
                  lung (n = 58, 31%), and breast (n = 59, 32.2%). In contrast, low percentages of posi-
                  tive tissue staining were observed for the cancer of liver (n = 60, 3.5%) and prostate
                  (n = 22, 10%). Based on the results, RP215 could be a unique probe for cancer diag-
                  nosis [12,13].
                     In recent years, evidence of circulating autoantibodies in the sera of patients with
                  cancer have created opportunities for utilizing the immune system as a source of
                  cancer biomarkers. Autoantibodies are used as serum biomarkers which show highly
                  appealing features. The persistence and stability of autoantibodies in the serum of
                  patients is a good point over other potential markers that have been currently utilized.
                  Autoantibodies are available in the sera before of TAAs can be detected (if they are).
                  They correspond to an effective biological amplification of the presence of TAAs,
                  and are released in the serum prior to initial clinical symptoms. Moreover, antibod-
                  ies are highly stable in serum samples and are not subjected to proteolysis like other
                  polypeptides, making sample handling much easier. They have shown a long life-
                  time (half-life between 7 and 30 days, depending on the type of Ig) in the blood
                  and may persist as long as the corresponding autoantigen creates a specific humoral
                  response. A few researches have attempted to identify panels of autoantibodies for
                  early diagnosis of breast cancer. The results were favorable, in some patients sensi-
                  tivities above 70% [14,15].
                     A summary of the recent studies on the use of autoantibody for the diagnosis of
                  cancers is given in Table 3.3.



                   Table 3.3  Autoantibodies associated with cancer detection.
                   TA
                   autoantibody  Cancer                                     Study
                   marker      type    Method            Sensitivity Specificity year  Ref.
                   P53         Lung    Immunoassay       76%      73.2%     2016  [16]
                   P16, c-myc,   Breast  Elisa           75%      90%       2017  [17]
                   ANAX-1
                   P53,CA19-9  Colorectal Elisa          47.1%    None      2016  [18]
                   Six peptide   Lung  Immunohistochemistry 95.6%  95.6%    2010  [19]
                   clones
   46   47   48   49   50   51   52   53   54   55   56