Table 1.
Summary of the various oncogenic and tumour suppressor roles previously ascribed for LGR5 in CRC
Main findings | Models and studies |
---|---|
Oncogenic roles for LGR5 in CRC | |
LGR5 is overexpressed in CRC | Primary human/mouse CRC and adenoma cells23–37 |
LGR5 expression predicts adverse prognosis | Primary human CRC;7,24,26,27,29 Meta-analyses41,42 |
LGR5 knockdown reduces proliferation, growth, migration, clonogenicity, invasion, PGE2-mediated survival and increases apoptosis, chemosensitivity | Human CRC cell lines;34,46–48 Human adenoma cell lines50 |
LGR5 overexpression increases proliferation and chemo-resistance | Human CRC cell lines27 |
LGR5 positivity confers greater clonogenic capacity | Human CRC cell lines and primary human CRC tumours49 |
Tumour suppressor roles for LGR5 in CRC | |
Loss of LGR5 expression during CRC progression | Human CRC cell lines and primary CRC tumours;50,53 Primary human CRC cells52 |
LGR5 expression predicts favourable prognosis | Primary human CRC52 |
LGR5 suppresses Wnt signalling | Mouse small intestine;54,55 Human CRC cell lines;56 Human CRC cell lines and primary human CRC tumours57,58 |
LGR5 knockdown increases invasion, growth, proliferation (including EGF-mediated) and tumourigenicity | Human CRC cell lines;56 Human adenoma cell lines51 |
LGR5 overexpression reduces proliferation | CRC cell lines;56 Human CRC cell lines and primary human CRC tumours57,58 |