| Literature DB >> 26582901 |
Melissa R Junttila1, Weiguang Mao2, Xi Wang2, Bu-Er Wang2, Thinh Pham2, John Flygare2, Shang-Fan Yu2, Sharon Yee2, David Goldenberg2, Carter Fields2, Jeffrey Eastham-Anderson2, Mallika Singh2, Rajesh Vij2, Jo-Anne Hongo2, Ron Firestein2, Melissa Schutten2, Kelly Flagella2, Paul Polakis2, Andrew G Polson1.
Abstract
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.Entities:
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Year: 2015 PMID: 26582901 DOI: 10.1126/scitranslmed.aac7433
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956