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NLRP12 has been shown to suppress colorectal tumorigenesis. However, the precise mechansim of NLRP12-mediated regualtion of colorectal cancer is unknown. Results: RNAseq data demonstrate higher expression of oncogenes, matrix degrading enzymes such as matrix metaloproteinases (MMPs), and genes involved in tumor invasion in Nlrp12-/- compared to wild-type tumors. Notably, several of the genes highly induced in Nlrp12-/- tumors are regulated by the Wnt/b-catenin pathway. Conclusion: NLRP12 negatively regualtes the Wnt/b-catenin pathway to suppress colorectal cancer progression and invasion. Overall design: Methods: Colorectal tumors were induced in wild-type and Nlrp12-/- mice with a single injection (i.p.) of azoxymethane followed by 3 cycles of 2.5% dextran sodium sulphate administration for 5 days in each cycle. Tumors were collected 12 weeks post azoxymethane treatment. RNA was isolated from tumors and analyzed by RNAseq.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>RNAseq analysis of gene expression in colorectal tumors of wild-type and Nlrp12-/- mice</name><description>RNAseq analysis of gene expression in colorectal tumors of wild-type and Nlrp12-/- mice</description><dates><last_updated>2025-09-24</last_updated><first_public>2020-10-02</first_public></dates><accession>PRJNA630077</accession><cross_references><GEO>GSE149769</GEO><taxon>10090</taxon></cross_references></HashMap>