组织因子
转移
胰腺癌
抗体
癌症研究
凝结
体内
医学
癌细胞
凝血活酶
体外
胰腺
癌症
病理
免疫学
生物
内科学
生物化学
生物技术
作者
Yohei Saito,Yuki Hashimoto,Jun-ichiro Kuroda,Masahiro Yasunaga,Yoshikatsu Koga,Amane Takahashi,Yasuhiro Matsumura
标识
DOI:10.1016/j.ejca.2011.04.028
摘要
Tissue factor (TF), the initiating cell surface receptor for the blood coagulation cascade, plays an important role in malignant transformation of the pancreas, although the precise mechanism remains unresolved. Here, we report that the TF – factor VIIa complex in human pancreatic cancer cells produced a significant amount of MMP-9 and promoted invasion ability in vitro and invasion and metastasis in vivo. For treatment, we successfully developed an anti-human TF monoclonal antibody that inhibits both cellular signalling and blood coagulation cascade via TF. Invasive capability and MMP-9 expression were significantly reduced by the antibody. The antibody inhibited not only tumour invasion in the orthotopic model, but also haematogenous metastasis in the portal-injection liver metastasis model. In conclusion, the TF-VIIa complex plays an important role in invasion-metastasis by enhancing tumour cell infiltration ability and forming microthrombi. The newly established anti-human TF neutralisation antibody may be useful for the treatment of pancreatic and other invasive cancers.
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