Single domain antibody against carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) inhibits proliferation, migration, invasion and angiogenesis of pancreatic cancer cells

癌胚抗原 血管生成 细胞粘附分子 癌症研究 抗体 胰腺癌 化学 细胞粘附 癌症 医学 细胞 免疫学 内科学 生物化学
作者
Tsai-Mu Cheng,Yanal Murad,Chia‐Ching Chang,Ming-Chi Yang,Toya Nath Baral,Aaron Cowan,Shin-Hua Tseng,Andrew Wong,Roger MacKenzie,Dar-Bin Shieh,Jianbing Zhang
出处
期刊:European Journal of Cancer [Elsevier]
卷期号:50 (4): 713-721 被引量:38
标识
DOI:10.1016/j.ejca.2012.07.019
摘要

Carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) is over-expressed in pancreatic cancer cells, and it is associated with the progression of pancreatic cancer. We tested a single domain antibody (sdAb) targeting CEACAM6, 2A3, which was isolated previously from a llama immune library, and an Fc conjugated version of this sdAb, to determine how they affect the pancreatic cancer cell line BxPC3. We also compared the effects of the antibodies to gemcitabine. Gemcitabine and 2A3 slowed down cancer cell proliferation. However, only 2A3 retarded cancer cell invasion, angiogenesis within the cancer mass and BxPC3 cell MMP-9 activity, three features important for tumour growth and metastasis. The IC50s for 2A3, 2A3-Fc and gemcitabine were determined as 6.5 μM, 8 μM and 12 nM, respectively. While the 2A3 antibody inhibited MMP-9 activity by 33% compared to non-treated control cells, gemcitabine failed to inhibit MMP-9 activity. Moreover, 2A3 and 2A3-Fc inhibited invasion of BxPC3 by 73% compared to non-treated cells. When conditioned media that were produced using 2A3- or 2A3-Fc-treated BxPC3 cells were used in a capillary formation assay, the capillary length was reduced by 21% and 49%, respectively. Therefore 2A3 is an ideal candidate for treating tumours that over-express CEACAM6.
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