Your browser doesn't support javascript.
loading
Targeting LGR5+ cells with an antibody-drug conjugate for the treatment of colon cancer.
Junttila, Melissa R; Mao, Weiguang; Wang, Xi; Wang, Bu-Er; Pham, Thinh; Flygare, John; Yu, Shang-Fan; Yee, Sharon; Goldenberg, David; Fields, Carter; Eastham-Anderson, Jeffrey; Singh, Mallika; Vij, Rajesh; Hongo, Jo-Anne; Firestein, Ron; Schutten, Melissa; Flagella, Kelly; Polakis, Paul; Polson, Andrew G.
Affiliation
  • Junttila MR; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA. polson@gene.com junttila.melissa@gene.com.
  • Mao W; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Wang X; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Wang BE; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Pham T; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Flygare J; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Yu SF; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Yee S; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Goldenberg D; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Fields C; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Eastham-Anderson J; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Singh M; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Vij R; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Hongo JA; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Firestein R; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Schutten M; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Flagella K; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Polakis P; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Polson AG; Research and Early Development, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA. polson@gene.com junttila.melissa@gene.com.
Sci Transl Med ; 7(314): 314ra186, 2015 Nov 18.
Article in En | MEDLINE | ID: mdl-26582901
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.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Neoplastic Stem Cells / Immunotoxins / Colonic Neoplasms / Receptors, G-Protein-Coupled / Antineoplastic Agents Type of study: Prognostic_studies Limits: Animals Language: En Journal: Sci Transl Med Journal subject: CIENCIA / MEDICINA Year: 2015 Type: Article

Full text: 1 Database: MEDLINE Main subject: Neoplastic Stem Cells / Immunotoxins / Colonic Neoplasms / Receptors, G-Protein-Coupled / Antineoplastic Agents Type of study: Prognostic_studies Limits: Animals Language: En Journal: Sci Transl Med Journal subject: CIENCIA / MEDICINA Year: 2015 Type: Article