It remains generally accepted that colorectal cancer (CRC) results from the accumulation of genetic events within the epithelial compartment. Unresolved issues include (1) whether the order of these genetic events matter (e.g., APC vs KRAS), (2) whether cancers can initiate from multiple distinct cells of origin, (3) the relationship between the normal colonic stem cell and the cells that function to maintain the tumor and (4) the contribution of the local environment to the neoplastic process. We hypothesize that colonic tumor initiation and progression is highly dependent upon the origin of the cell that incurs the relevant mutagenic events, as well as the regulation of growth and clonal selection of particular progeny that emanate from tumor-initiating cells. We have demonstrated that there are distinct normal colonic progenitor populations marked by expression of two specific cell surface markers, Lrig1 and Lgr5. Although the precise relationship between cells expressing these two markers is unknown, these two bona fide stem cell markers exhibit overlapping, yet distinct, expression patterns in both normal colon and in ApcMin/+ tumors. Of note, Lrig1 is induced by EGFR signaling and acts to negatively regulate EGFR signaling, whereas Lgr5 is a canonical Wnt target of unknown function. We have generated inducible Lrig1-CreERT2 mice, and our collaborator Hans Clevers has provided us with inducible Lgr5-EGFP-IRES-CreERT2 animals that allow for the specific activation of Cre recombinase within distinct colonic stem cell populations. We will use these mice to determine the importance of cell-of-origin in colon cancer initiation and progression. In addition, we have identified a gene, Slc26a3, that is selectively expressed in the differentiated compartment of the colon, and we have generated Slc26a3-CreERT2 mice that will allow us to resolve whether colonic tumors arise from the """"""""top down"""""""" or """"""""bottom up.""""""""

Public Health Relevance

The cell in the colon which gives rise to colorectal cancer is unknown. We have generated novel genetically engineered mice that will allow us to answer this question. These results may allow us to determine whether colon cancer stem cells exist and their relationship to normal colonic stem cells, leading to identification of the colon cancer cell-of-origin and the colon cancer stem cell and offering exciting new therapeutic options.

National Institute of Health (NIH)
National Cancer Institute (NCI)
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Molecular Oncogenesis Study Section (MONC)
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Salnikow, Konstantin
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Vanderbilt University Medical Center
Internal Medicine/Medicine
Schools of Medicine
United States
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Wang, Yang; Shi, Chanjuan; Lu, Yuanyuan et al. (2015) Loss of Lrig1 leads to expansion of Brunner glands followed by duodenal adenomas with gastric metaplasia. Am J Pathol 185:1123-34
Gierut, Jessica J; Lyons, Jesse; Shah, Manasvi S et al. (2015) Oncogenic K-Ras promotes proliferation in quiescent intestinal stem cells. Stem Cell Res 15:165-71
Kondo, Jumpei; Powell, Anne E; Wang, Yang et al. (2015) LRIG1 Regulates Ontogeny of Smooth Muscle-Derived Subsets of Interstitial Cells of Cajal in Mice. Gastroenterology 149:407-19.e8
Gierut, Jessica J; Jacks, Tyler E; Haigis, Kevin M (2014) In vivo delivery of lenti-Cre or adeno-Cre into mice using intranasal instillation. Cold Spring Harb Protoc 2014:307-9
Singh, Bhuminder; Coffey, Robert J (2014) From wavy hair to naked proteins: the role of transforming growth factor alpha in health and disease. Semin Cell Dev Biol 28:12-21
Powell, Anne E; Vlacich, Gregory; Zhao, Zhen-Yang et al. (2014) Inducible loss of one Apc allele in Lrig1-expressing progenitor cells results in multiple distal colonic tumors with features of familial adenomatous polyposis. Am J Physiol Gastrointest Liver Physiol 307:G16-23
Poulin, Emily J; Powell, Anne E; Wang, Yang et al. (2014) Using a new Lrig1 reporter mouse to assess differences between two Lrig1 antibodies in the intestine. Stem Cell Res 13:422-30
Gierut, Jessica J; Jacks, Tyler E; Haigis, Kevin M (2014) Strategies to achieve conditional gene mutation in mice. Cold Spring Harb Protoc 2014:339-49
Gierut, Jessica J; Jacks, Tyler E; Haigis, Kevin M (2014) Whole-mount X-Gal staining of mouse tissues. Cold Spring Harb Protoc 2014:417-9
Gierut, Jessica J; Jacks, Tyler E; Haigis, Kevin M (2014) Producing and concentrating lenti-Cre for mouse infections. Cold Spring Harb Protoc 2014:304-6

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