乳腺癌
抗体
单克隆抗体
重组DNA
癌症研究
癌症
免疫组织化学
流式细胞术
上皮细胞粘附分子
医学
血管生成
生物
免疫学
内科学
生物化学
基因
作者
Roya Mirzaei,Soodabeh Shafiee,Rana Vafaei,Malihe Salehi,Neda Jalili,Zahra Nazerian,Ahad Muhammadnajad,Fatemeh Yadegari,Mohamad Reza Esmailinejad,Leila Farahmand
标识
DOI:10.1016/j.intimp.2023.110656
摘要
The utilization of monoclonal antibodies (moAbs), an issue correlated with the biopharmaceutical professions, is developing and maturing. Coordinated with this conception, we produced the appealingly modeled anti-EpCAM scFv for breast cancer tumors.Afterward cloning and expression of recombinant antibody in Escherichia coli bacteria, the correctness of the desired antibody was checked by western blotting. Flow cytometry was utilized to determine the capacity of the recombinant antibody to append to the desired receptors in the malignant breast cancer (BC)cell line. The recombinant antibody (anti-EpCAM scFv) was examined for preclinical efficacy in reducing tumor growth, angiogenesis, and invasiveness (in vitro- in vivo).A target antibody-mediated attenuation of migration and invasion in the examined cancer cell lines was substantiated (P-value < 0.05). Grafted tumors from breast cancer in mice indicated significant and compelling suppression of tumor growth and decrement in blood supply in reaction to the recombinant anti-EpCAM intervention. Evaluations of immunohistochemical and histopathological findings revealed an enhanced response rate to the treatment.The desired anti-EpCAM scFv can be a therapeutic tool to reduce invasion and proliferation in malignant breast cancer.
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