医学
伊立替康
紫杉醇
癌症研究
贝伐单抗
催眠药
联合疗法
体内
单克隆抗体
癌症
化疗
肿瘤微环境
抗体
结直肠癌
药理学
肿瘤科
内科学
免疫学
生物
生物技术
作者
Dong-Hoon Yeom,Yo-Seob Lee,Ilhwan Ryu,Sunju Lee,Byungje Sung,Hanbyul Lee,Dongin Kim,Jin-Hyung Ahn,Eunsin Ha,Yong‐Soo Choi,Sang Hoon Lee,Weon‐Kyoo You
摘要
Delta-like-ligand 4 (DLL4) is a promising target to augment the effects of VEGF inhibitors. A simultaneous blockade of VEGF/VEGFR and DLL4/Notch signaling pathways leads to more potent anti-cancer effects by synergistic anti-angiogenic mechanisms in xenograft models. A bispecific antibody targeting VEGF and DLL4 (ABL001/NOV1501/TR009) demonstrates more potent in vitro and in vivo biological activity compared to VEGF or DLL4 targeting monoclonal antibodies alone and is currently being evaluated in a phase 1 clinical study of heavy chemotherapy or targeted therapy pre-treated cancer patients (ClinicalTrials.gov Identifier: NCT03292783). However, the effects of a combination of ABL001 and chemotherapy on tumor vessels and tumors are not known. Hence, the effects of ABL001, with or without paclitaxel and irinotecan were evaluated in human gastric or colon cancer xenograft models. The combination treatment synergistically inhibited tumor progression compared to each monotherapy. More tumor vessel regression and apoptotic tumor cell induction were observed in tumors treated with the combination therapy, which might be due to tumor vessel normalization. Overall, these findings suggest that the combination therapy of ABL001 with paclitaxel or irinotecan would be a better clinical strategy for the treatment of cancer patients.
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