ATF6 activation alters colonic lipid metabolism causing tumor-associated microbial adaptation
Coleman, O. I.; Sorbie, A.; Riva, A.; von Stern, M.; Kuhls, S.; Selegato, D.; Koehler, N.; Wirbel, J.; Kacprowski, T.; Dunkel, A.; Pauling, J. K.; Plagge, J.; Miedel-Cuadra, D.; Wagner, S.; Chadly, I.; Bierwirth, S.; Peng, T.; Metzler, T.; Schafmayer, C.; Hinz, S.; Roeder, C.; Roecken, C.; Zimmermann, M.; Rosenstiel, P.; Steiger, K.; Jesinghaus, M.; Liebisch, G.; Ecker, J.; Schmidt, C.; Zeller, G.; Janssen, K.-P.; Haller, D.
Show abstract
Endoplasmic reticulum unfolded protein responses (UPRER) contribute to cancer development and the activating transcription factor 6 (ATF6) is involved in microbiota-dependent tumorigenesis. Here, we substantiate the clinical relevance of ATF6 in early-onset and late colorectal cancer patient cohorts. Transcriptional analysis in intestinal epithelial cells (IEC) of ATF6 transgenic mice (nATF6IEC) identified bacteria-specific changes in cellular metabolism enriched for fatty acid biosynthesis. Untargeted metabolomics and isotype-labeling confirmed ATF6-related enrichment of long chain fatty acids in colonic tissue of patients, mice and organoid cultures. FASN inhibition and microbiota transfer in germ-free nATF6IEC mice confirmed the causal involvement of ATF6-induced lipid alterations in tumorigenesis. The selective expansion of tumor-relevant microbial taxa was mechanistically linked to long chain fatty acid exposure, using bioorthogonal non-canonical amino acid tagging (BONCAT) and growth analysis of Desulfovibrio isolates. We postulate chronic ATF6 signaling in the epithelium to select for tumor-promoting microbiota by altering lipid metabolism. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=126 SRC="FIGDIR/small/565267v2_ufig1.gif" ALT="Figure 1"> View larger version (31K): org.highwire.dtl.DTLVardef@be3756org.highwire.dtl.DTLVardef@231da4org.highwire.dtl.DTLVardef@16f3aaeorg.highwire.dtl.DTLVardef@1758fe3_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOGraphical Abstract:C_FLOATNO Chronic ATF6 signaling in the colonic epithelium alters lipid metabolism to select a tumor-promoting microbiota C_FIG O_LIBiallelic expression of activated ATF6 (p50 nuclear fragment) in intestinal epithelial cells (nATF6IEC) induces spontaneous colon tumors in SPF but not GF mice C_LIO_LIMechanistically, biallelic SPF nATF6IEC mice alter colonic lipid metabolism, including the upregulation of LCFAs and Fasn C_LIO_LIInhibition of FASN prevents colon tumor formation in mice, and reduces the tumor-promoting potential of the intestinal microbiota (FMT) C_LIO_LIExposure of fl/fl control mouse microbiota to LCFAs ex vivo translationally activates tumor-associated bacteria, including Desulfovibrio fairfieldensis C_LIO_LIHuman CRC patients show ATF6 upregulation, FASN co-occurrence and increased LCFAs in T tissue C_LIO_LIATF6 activity links with CRC-associated microbiota in patients, including Desulfovibrio C_LI Created with BioRender.com nATF6: activated activating transcription factor 6; LCFA: long-chain fatty acids; SAFA: saturated fatty acids; Fasn: fatty acid synthase; C75 i.p.: intraperitoneal injection of the Fasn inhibitor C75.
Matching journals
The top 2 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Accelerated cognitive decline in obese mouse model of Alzheimer's disease is linked to sialic acid-driven immune deregulation 97%
- YAP-Driven Oral Epithelial Stem Cell Malignant Reprogramming at Single Cell Resolution 97%
- Widespread transfer of mobile antibiotic resistance genes within individual gut microbiomes revealed through bacterial Hi-C 97%
Similar papers in this journal
- Epithelial zonation along the mouse and human small intestine defines five discrete metabolic domains 98%
- A biomechanical switch regulates the transition towards homeostasis in esophageal epithelium 97%
- Cyclophilin A regulates protein phase separation and mitigates haematopoietic stem cell aging 97%
Similar papers in this journal
- Identifying cardiac actinin interactomes reveals sarcomere crosstalk with RNA-binding proteins 96%
- Interrogating Metabolic Interactions Between Skeletal Muscle and Liver Circadian Clocks In Vivo 96%
- Distinct Subsets of Multi-Lymphoid Progenitors Support Ontogeny-Related Changes in Human Lymphopoiesis 96%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.