Matches in SemOpenAlex for { <https://semopenalex.org/work/W3136248097> ?p ?o ?g. }
- W3136248097 endingPage "460" @default.
- W3136248097 startingPage "448" @default.
- W3136248097 abstract "Three-dimensional (3D) biomaterials with physiologically relevant and experimentally tractable biomechanical features are important platforms to advance our understanding of the influence of tissue mechanics in disease progression. Herein, an interpenetrating network (IPN) of collagen and alginate 3D culture system with tunable extracellular microstructure and mechanics is exploited as a tumor stroma proxy to study phenotypic plasticity of colorectal cancer-associated fibroblasts (CAF). In combination with Next Generation Sequencing (NGS) data analysis, we demonstrated that tuning the storage modulus of the IPN hydrogel between 49 and 419 Pa can trigger a reversible switch between an inflammatory (i-state, α-SMAlowIL-6high) and myofibroblastic (m-state, α-SMAhighIL-6low) state in CAF that is dependent on the polymer network confinement effect and ROS-HIF1-α mechanotransduction signaling axis. Secretome from m-state CAF upregulated several epithelial-mesenchymal-transition (EMT) transcripts and induced robust scattering in DLD-1, HCT116, and SW480 human colorectal adenocarcinoma, while the EMT-inducing capacity is muted in i-state CAF, suggestive of an anti-tumorigenic role. Our findings were further validated through Gene Expression Profiling Interactive Analysis (GEPIA), which showed that cytokines secreted at higher levels by i-state CAF are correlated (p < 0.05) with good overall colorectal cancer patient survival. Therefore, 3D network density and spatial cellular confinement are critical biophysical determinants that can profoundly influence CAF states, paracrine signaling, and EMT-inducing potential. The communication between cancer cells and cancer-associated fibroblasts (CAF) contributes to tumor metastasis. CAF represent a diverse population of cellular subsets that can either promote or restrain tumor progression. However, the origin and cause of CAF heterogeneity remain elusive, limiting CAF-directed therapies for clinical use. We studied the dynamic phenotypes of CAF using a 3D physio-mimetic culture platform consisting of an interpenetrating collagen-alginate network. Combined with transcriptomic stratification and correlative analysis using cancer patient dataset, we showed phenotypic interconversion between inflammatory and myofibroblastic states, with anti- and pro-tumorigenic functions, in human colorectal CAF. This multidisciplinary study reveals the functional diversity of colorectal CAF caused by biophysical cues. The finding will influence the development of new CAF biomarkers and cancer therapies." @default.
- W3136248097 created "2021-03-29" @default.
- W3136248097 creator A5022769862 @default.
- W3136248097 creator A5035811659 @default.
- W3136248097 creator A5059974201 @default.
- W3136248097 creator A5076578237 @default.
- W3136248097 creator A5079132263 @default.
- W3136248097 date "2021-09-01" @default.
- W3136248097 modified "2023-10-10" @default.
- W3136248097 title "A 3D physio-mimetic interpenetrating network-based platform to decode the pro and anti-tumorigenic properties of cancer-associated fibroblasts" @default.
- W3136248097 cites W1553351438 @default.
- W3136248097 cites W1940485834 @default.
- W3136248097 cites W1972196680 @default.
- W3136248097 cites W1999133016 @default.
- W3136248097 cites W2000241906 @default.
- W3136248097 cites W2017818722 @default.
- W3136248097 cites W2040670989 @default.
- W3136248097 cites W2058187251 @default.
- W3136248097 cites W2072703892 @default.
- W3136248097 cites W2077462602 @default.
- W3136248097 cites W2088110734 @default.
- W3136248097 cites W2092893236 @default.
- W3136248097 cites W2105699441 @default.
- W3136248097 cites W2109663830 @default.
- W3136248097 cites W2119203258 @default.
- W3136248097 cites W2131673566 @default.
- W3136248097 cites W2134659158 @default.
- W3136248097 cites W2267049176 @default.
- W3136248097 cites W2336782981 @default.
- W3136248097 cites W2338391827 @default.
- W3136248097 cites W2411980485 @default.
- W3136248097 cites W2510973356 @default.
- W3136248097 cites W2512931560 @default.
- W3136248097 cites W2526266802 @default.
- W3136248097 cites W2590146273 @default.
- W3136248097 cites W2590390825 @default.
- W3136248097 cites W2603666401 @default.
- W3136248097 cites W2607129810 @default.
- W3136248097 cites W2726732890 @default.
- W3136248097 cites W2734617308 @default.
- W3136248097 cites W2762514399 @default.
- W3136248097 cites W2765776870 @default.
- W3136248097 cites W2771542157 @default.
- W3136248097 cites W2786031287 @default.
- W3136248097 cites W2786843484 @default.
- W3136248097 cites W2797953889 @default.
- W3136248097 cites W2807387796 @default.
- W3136248097 cites W2902414453 @default.
- W3136248097 cites W2904125616 @default.
- W3136248097 cites W2906067435 @default.
- W3136248097 cites W2907695702 @default.
- W3136248097 cites W2912815018 @default.
- W3136248097 cites W2973099177 @default.
- W3136248097 cites W2974381971 @default.
- W3136248097 cites W3017611767 @default.
- W3136248097 cites W3022615893 @default.
- W3136248097 cites W3076678262 @default.
- W3136248097 cites W3084144173 @default.
- W3136248097 doi "https://doi.org/10.1016/j.actbio.2021.03.037" @default.
- W3136248097 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33766799" @default.
- W3136248097 hasPublicationYear "2021" @default.
- W3136248097 type Work @default.
- W3136248097 sameAs 3136248097 @default.
- W3136248097 citedByCount "16" @default.
- W3136248097 countsByYear W31362480972021 @default.
- W3136248097 countsByYear W31362480972022 @default.
- W3136248097 countsByYear W31362480972023 @default.
- W3136248097 crossrefType "journal-article" @default.
- W3136248097 hasAuthorship W3136248097A5022769862 @default.
- W3136248097 hasAuthorship W3136248097A5035811659 @default.
- W3136248097 hasAuthorship W3136248097A5059974201 @default.
- W3136248097 hasAuthorship W3136248097A5076578237 @default.
- W3136248097 hasAuthorship W3136248097A5079132263 @default.
- W3136248097 hasBestOaLocation W31362480971 @default.
- W3136248097 hasConcept C104317684 @default.
- W3136248097 hasConcept C121608353 @default.
- W3136248097 hasConcept C127561419 @default.
- W3136248097 hasConcept C170493617 @default.
- W3136248097 hasConcept C181104049 @default.
- W3136248097 hasConcept C189165786 @default.
- W3136248097 hasConcept C192562407 @default.
- W3136248097 hasConcept C2779013556 @default.
- W3136248097 hasConcept C2779256057 @default.
- W3136248097 hasConcept C2908647359 @default.
- W3136248097 hasConcept C502942594 @default.
- W3136248097 hasConcept C526805850 @default.
- W3136248097 hasConcept C54355233 @default.
- W3136248097 hasConcept C71924100 @default.
- W3136248097 hasConcept C76419328 @default.
- W3136248097 hasConcept C7876069 @default.
- W3136248097 hasConcept C86803240 @default.
- W3136248097 hasConcept C95444343 @default.
- W3136248097 hasConcept C96232424 @default.
- W3136248097 hasConcept C99454951 @default.
- W3136248097 hasConceptScore W3136248097C104317684 @default.
- W3136248097 hasConceptScore W3136248097C121608353 @default.
- W3136248097 hasConceptScore W3136248097C127561419 @default.
- W3136248097 hasConceptScore W3136248097C170493617 @default.