LGR5型
结合
癌症研究
药品
癌症
抗体-药物偶联物
抗体
结直肠癌
贝伐单抗
免疫学
单克隆抗体
药理学
医学
化疗
内科学
数学分析
数学
作者
Melissa R. Junttila,Weiguang Mao,Xi Wang,Bu-er Wang,Thinh Pham,John A. Flygare,Shang-Fan Yu,Sharon Yee,David M. Goldenberg,Carter T. Fields,Jeffrey Eastham‐Anderson,Mallika Singh,Rajesh Vij,Jo-Anne Hongo,Ron Firestein,Melissa M. Schutten,Kelly M. Flagella,Paul Polakis,Andrew G. Polson
标识
DOI:10.1126/scitranslmed.aac7433
摘要
Cancer stem cells (CSCs) are hypothesized to actively maintain tumors similarly to how their normal counterparts replenish differentiated cell types within tissues, making them an attractive therapeutic target for the treatment of cancer. Because most CSC markers also label normal tissue stem cells, it is unclear how to selectively target them without compromising normal tissue homeostasis. We evaluated a strategy that targets the cell surface leucine-rich repeat-containing G protein-coupled receptor 5 (LGR5), a well-characterized tissue stem cell and CSC marker, with an antibody conjugated to distinct cytotoxic drugs. One antibody-drug conjugate (ADC) demonstrated potent tumor efficacy and safety in vivo. Furthermore, the ADC decreased tumor size and proliferation, translating to improved survival in a genetically engineered model of intestinal tumorigenesis. These data demonstrate that ADCs can be leveraged to exploit differences between normal and cancer stem cells to successfully target gastrointestinal cancers.
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