INTESTINAL CANCERS & DISEASES Dysregulated CRTC1 Activity Is a Novel Component of PGE2 Signaling that Contributes to Colon Cancer Growth Researchers provide evidence of enhanced CRTC1 (CREB-regulated transcription co-activator 1) protein content and transcriptional activity in mouse models of sporadic or colitis-associated colon cancer azoxymethane/dextran sulfate sodium, and in human colorectal tumors specimens compared with adjacent normal mucosa. [Oncogene] Abstract Intestinal-Specific Activatable Myb Initiates Colon Tumorigenesis in Mice Investigators generated the first intestinal-specific, inducible transgenic model; a MybER transgene encoding a tamoxifen-inducible fusion protein between Myb and the estrogen receptor-α ligand-binding domain driven by the intestinal-specific promoter, Gpa33. [Oncogene] Abstract DNMT1-Associated Long Non-Coding RNAs Regulate Global Gene Expression and DNA Methylation in Colon Cancer Researchers tested if long non-coding (lnc)RNAs could associate with DNA methyltransferases to regulate DNA methylation and gene expression. Using RIP-seq, scientists identified a subset of lncRNAs that interact with the DNA methyltransferase DNMT1 in a colon cancer cell line, HCT116. [Hum Mol Genet] Abstract Enhanced Anti-Colon Cancer Immune Responses with Modified eEF2-Derived Peptides Scientists indicated that modifications of a segment of peptides from wild type eukaryotic elongation factor-2 (eEF2)-derived immunogenic peptides was able to further enhance its capacity of inducing antigen-specific cytotoxic T lymphocytes against colon cancer cells. [Cancer Lett] Abstract Hsa-miR-19a Is Associated with Lymph Metastasis and Mediates the TNF-α Induced Epithelial-to-Mesenchymal Transition in Colorectal Cancer The authors reported that high expression of microRNA-19a (miR-19a) was associated with lymph node metastasis and played an important role in TNF-α-induced epithelial-to-mesenchymal transition in colorectal cancer cells. [Sci Rep] Full Abstract Glial Cell Line-Derived Neurotrophic Factor (GDNF) Promotes Barrier Maturation and Wound Healing in Intestinal Epithelial Cells In Vitro Scientists showed that enterocytes represent an additional source of GDNF synthesis. GDNF contributed to wound healing in a cAMP/PKA-dependent manner and promoted barrier maturation in immature enterocytes cells by inactivation of p38MAPK signaling. [Am J Physiol Gastrointest Liver Physiol] Abstract Loss of Histone Deacetylase Hdac1 Disrupts Metabolic Processes in Intestinal Epithelial Cells Scientists showed that Hdac1 depletion in cellulo leads to increased histone acetylation after metabolic stresses, and to metabolic disturbances resulting in impaired responses to oxidative stresses, AMPK kinase activation and mitochondrial biogenesis. [FEBS Lett] Abstract INTESTINAL STEM CELL & ORGANOID RESEARCH A Mouse Model of Targeted Musashi1 Expression in Whole Intestinal Epithelium Suggests Regulatory Roles in Cell Cycle and Stemness The authors generated a mouse model, referred to as v-Msi, overexpressing Musashi1 specifically in the entire intestinal epithelium. Compared with wild type litters, v-Msi1 mice exhibited increased intestinal crypt size accompanied by enhanced proliferation. Comparative transcriptomics by RNA-seq revealed Musashi1’s association with gut stem cell signature, cell cycle, DNA replication and drug metabolism. [Stem Cells] Abstract Ttk69 Acts as a Master Repressor of Enteroendocrine Cell Specification in Drosophila Intestinal Stem Cell Lineages Scientists identified Ttk69, a BTB domain-containing transcriptional repressor, as a master repressor of enteroendocrine cell specification in the intestinal stem cell lineages. [Development] Abstract |