Doctoral Program in Medical Science, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia.
Urology Department, Faculty of Medicine, Universitas Brawijaya, Saiful Anwar Hospital, Malang.
Asian Pac J Cancer Prev. 2023 Sep 1;24(9):3155-3164. doi: 10.31557/APJCP.2023.24.9.3155.
This study will identify specific epitopes from the 47kDa protein as the basis for making polyclonal antibodies to increasing sensitivity and specificity of 47kDa protein as bladder cancer biomarkers.
The 47kDa protein epitope prediction was carried out using the in-silico method. The epitope with the highest and the lowest value was immunized to the mice for four weeks and was harvested at the fifth weeks. The antibody was tested with the patient's urine using western blotting. Total of 186 participants including in this study. For the first stage (antibody confirmation test) test we have 18 participants, for the second stage (1st antibody diagnosis test) we have 72 participants and for the third stage (2nd antibody diagnosis test) we have 96 participants, consist of total 64 BC patients 48 of healthy individuals and 74 participants with the other diseases.
Some epitopes from the sequenced protein are candidates for immunization, in the chain 108'-136' (with lowest Bepipred score: 0.53) named as peptide1 and chain 42'-56' (with highest bepipred score: 0.58) named as peptide2. In western blotting test, both antibodies showed detection at 47kDa. When examined with western blot using urine from BC patients, urine from other cancer patients (prostate, kidney, ureter, rectal, breast), and healthy persons, both antibodies were found to only express 47kDa in urine from BC patients. The diagnostic tests showed high sensitivity (91.67%) and specificity (94.44%) inAb2 in predicting bladder cancer.
The evolution of the polyclonal antibody made from specific epitopes is proven to express specifically on bladder cancer patients and have high sensitivity and specificity to diagnose bladder cancer.
本研究将确定 47kDa 蛋白中的特定表位,以此为基础制备多克隆抗体,以提高 47kDa 蛋白作为膀胱癌生物标志物的灵敏度和特异性。
采用计算机方法预测 47kDa 蛋白表位。用免疫原性最高和最低的表位对小鼠进行免疫 4 周,第 5 周采集。用 Western blot 法检测抗体与患者尿液的反应。本研究共纳入 186 例患者。第一阶段(抗体确认试验)有 18 例患者,第二阶段(第一抗体诊断试验)有 72 例患者,第三阶段(第二抗体诊断试验)有 96 例患者,包括 64 例 BC 患者,48 例健康个体和 74 例其他疾病患者。
从测序蛋白中发现一些表位可作为免疫原,在链 108'-136'(Bepipred 评分最低:0.53)命名为肽 1 和链 42'-56'(Bepipred 评分最高:0.58)命名为肽 2。在 Western blot 试验中,两种抗体均在 47kDa 处检测到。用 BC 患者尿液、其他癌症患者(前列腺、肾脏、输尿管、直肠、乳腺)和健康个体尿液进行 Western blot 检测时,发现两种抗体仅在 BC 患者尿液中表达 47kDa。诊断试验显示 Ab2 预测膀胱癌的灵敏度(91.67%)和特异性(94.44%)均较高。
从特定表位进化而来的多克隆抗体被证明特异性表达于膀胱癌患者,对膀胱癌的诊断具有较高的灵敏度和特异性。