Compositions and methods for treating and diagnosing cancer
The present invention relates to compositions and methods for characterizing, diagnosing and treating cancer. In particular, the present invention identifies LGR5 as a protein over-expressed in solid tumor stem cell. The present invention further identifies an interaction between RSPO1 and LGR5 as an alternative pathway for the activation of beta-catenin signaling. In certain embodiments, the present invention provides biomolecules that disrupt functional signaling via a LGR protein, including, in certain embodiments, molecules that inhibit the interaction between one or more RSPO proteins and one or more LGR proteins, such as LGR5. In certain embodiments, the present invention provides methods of treating cancer comprising disrupting functional LGR signaling and inhibiting growth of a solid tumor comprising solid tumor stem cells.
1. An isolated chimeric, humanized, or human monoclonal antibody that (a) disrupts binding of a human R-spondin (RSPO) protein to a leucine-rich repeat-containing G protein-coupled receptor (LGR) protein, and/or (b) disrupts RSPO activation of LGR signaling.
2. The antibody of claim 1 , wherein the LGR protein is LGR5.
3. The antibody of claim 1 , which is an antibody fragment.
4. A cell line producing the antibody of claim 1 .
5. The isolated antibody of claim 1 , wherein said antibody specifically binds to a human RSPO protein selected from the group consisting of: RSPO1, RSPO2, RSPO3, and RSPO4.
6. The isolated antibody of claim 5 , wherein said antibody disrupts binding of the RSPO protein to a LGR protein.
7. The isolated antibody of claim 5 , wherein said antibody disrupts RSPO activation of LGR signaling.