{"title":"基于氧化右旋糖酐和硫代壳聚糖的水凝胶驱动仿生三阴性乳腺癌3D体外模型,用于癌症进展和治疗研究。","authors":"Unnati Modi, Pooja Makwana, Bindiya Dhimmar, Soundharya Ramu, Mohit Kumar Jolly, Rajesh Vasita","doi":"10.1039/d5tb00812c","DOIUrl":null,"url":null,"abstract":"<p><p>In the advancing field of <i>in vitro</i> cancer modeling, three-dimensional (3D) culture systems are increasingly recognized for their ability to recapitulate critical tumor-specific characteristics. Given the aggressive nature and high mortality associated with triple-negative breast cancer (TNBC), there is a pressing need to develop physiologically relevant 3D <i>in vitro</i> models that effectively simulate key tumor promoting factors (TPFs). This study presents a modified dextran-chitosan (MDC) hydrogel with engineered non-fouling properties that supports the formation of MDA-MB-231-derived 3D tumoroids. The hydrogel facilitated upregulated expression of extracellular matrix markers, including COL1A1 (2.29-fold↑) and FN1 (0.84-fold↑). Cell proliferation within 3D cultures was significantly reduced on days 2 (<i>p</i> < 0.001), 4 (<i>p</i> < 0.0001), and 6 (<i>p</i> < 0.001) compared to 2D cultures. Enhanced hypoxic conditions (based on EF5 adducts' fluorescence; <i>p</i> < 0.0001), epithelial-to-mesenchymal transition (EMT) traits, and stemness marker expression [<i>e.g.</i>, NANOG (3.33-fold↑)] were observed in 3D tumoroids. Additionally, the 3D tumor microenvironment showed elevated activity of key TPFs, including IL6, IL10, TNFA, FGF2, BMP2, and active TGFB (<i>p</i> < 0.0001). The MDC hydrogel, with stiffness mimicking breast tissue (∼11 kPa), also promoted mechanotransducive signalling, evidenced by increased YAP1 expression (2.4-fold↑) and a significantly elevated nuclear-to-cytoplasmic YAP1 ratio (<i>p</i> < 0.0001) relative to 2D cultures on TCPS (∼3 GPa). Whole transcriptome sequencing and gene set enrichment analyses further validated the enhanced tumorigenic phenotype of the 3D model. Moreover, the 3D tumoroids exhibited significant resistance (<i>p</i> < 0.001) to combined doxorubicin-paclitaxel treatment. Thus, the MDC hydrogel-based 3D TNBC model emerges as a robust and scalable platform for anticancer drug screening, evaluating precision medicine and investigating cancer biology.</p>","PeriodicalId":94089,"journal":{"name":"Journal of materials chemistry. B","volume":" ","pages":""},"PeriodicalIF":5.7000,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An oxidized dextran and thiolated chitosan-based hydrogel driven biomimetic triple negative breast cancer 3D <i>in vitro</i> model for cancer progression and therapeutic studies.\",\"authors\":\"Unnati Modi, Pooja Makwana, Bindiya Dhimmar, Soundharya Ramu, Mohit Kumar Jolly, Rajesh Vasita\",\"doi\":\"10.1039/d5tb00812c\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In the advancing field of <i>in vitro</i> cancer modeling, three-dimensional (3D) culture systems are increasingly recognized for their ability to recapitulate critical tumor-specific characteristics. Given the aggressive nature and high mortality associated with triple-negative breast cancer (TNBC), there is a pressing need to develop physiologically relevant 3D <i>in vitro</i> models that effectively simulate key tumor promoting factors (TPFs). This study presents a modified dextran-chitosan (MDC) hydrogel with engineered non-fouling properties that supports the formation of MDA-MB-231-derived 3D tumoroids. The hydrogel facilitated upregulated expression of extracellular matrix markers, including COL1A1 (2.29-fold↑) and FN1 (0.84-fold↑). Cell proliferation within 3D cultures was significantly reduced on days 2 (<i>p</i> < 0.001), 4 (<i>p</i> < 0.0001), and 6 (<i>p</i> < 0.001) compared to 2D cultures. Enhanced hypoxic conditions (based on EF5 adducts' fluorescence; <i>p</i> < 0.0001), epithelial-to-mesenchymal transition (EMT) traits, and stemness marker expression [<i>e.g.</i>, NANOG (3.33-fold↑)] were observed in 3D tumoroids. Additionally, the 3D tumor microenvironment showed elevated activity of key TPFs, including IL6, IL10, TNFA, FGF2, BMP2, and active TGFB (<i>p</i> < 0.0001). The MDC hydrogel, with stiffness mimicking breast tissue (∼11 kPa), also promoted mechanotransducive signalling, evidenced by increased YAP1 expression (2.4-fold↑) and a significantly elevated nuclear-to-cytoplasmic YAP1 ratio (<i>p</i> < 0.0001) relative to 2D cultures on TCPS (∼3 GPa). Whole transcriptome sequencing and gene set enrichment analyses further validated the enhanced tumorigenic phenotype of the 3D model. Moreover, the 3D tumoroids exhibited significant resistance (<i>p</i> < 0.001) to combined doxorubicin-paclitaxel treatment. Thus, the MDC hydrogel-based 3D TNBC model emerges as a robust and scalable platform for anticancer drug screening, evaluating precision medicine and investigating cancer biology.</p>\",\"PeriodicalId\":94089,\"journal\":{\"name\":\"Journal of materials chemistry. B\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":5.7000,\"publicationDate\":\"2025-10-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of materials chemistry. B\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/d5tb00812c\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of materials chemistry. B","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/d5tb00812c","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
An oxidized dextran and thiolated chitosan-based hydrogel driven biomimetic triple negative breast cancer 3D in vitro model for cancer progression and therapeutic studies.
In the advancing field of in vitro cancer modeling, three-dimensional (3D) culture systems are increasingly recognized for their ability to recapitulate critical tumor-specific characteristics. Given the aggressive nature and high mortality associated with triple-negative breast cancer (TNBC), there is a pressing need to develop physiologically relevant 3D in vitro models that effectively simulate key tumor promoting factors (TPFs). This study presents a modified dextran-chitosan (MDC) hydrogel with engineered non-fouling properties that supports the formation of MDA-MB-231-derived 3D tumoroids. The hydrogel facilitated upregulated expression of extracellular matrix markers, including COL1A1 (2.29-fold↑) and FN1 (0.84-fold↑). Cell proliferation within 3D cultures was significantly reduced on days 2 (p < 0.001), 4 (p < 0.0001), and 6 (p < 0.001) compared to 2D cultures. Enhanced hypoxic conditions (based on EF5 adducts' fluorescence; p < 0.0001), epithelial-to-mesenchymal transition (EMT) traits, and stemness marker expression [e.g., NANOG (3.33-fold↑)] were observed in 3D tumoroids. Additionally, the 3D tumor microenvironment showed elevated activity of key TPFs, including IL6, IL10, TNFA, FGF2, BMP2, and active TGFB (p < 0.0001). The MDC hydrogel, with stiffness mimicking breast tissue (∼11 kPa), also promoted mechanotransducive signalling, evidenced by increased YAP1 expression (2.4-fold↑) and a significantly elevated nuclear-to-cytoplasmic YAP1 ratio (p < 0.0001) relative to 2D cultures on TCPS (∼3 GPa). Whole transcriptome sequencing and gene set enrichment analyses further validated the enhanced tumorigenic phenotype of the 3D model. Moreover, the 3D tumoroids exhibited significant resistance (p < 0.001) to combined doxorubicin-paclitaxel treatment. Thus, the MDC hydrogel-based 3D TNBC model emerges as a robust and scalable platform for anticancer drug screening, evaluating precision medicine and investigating cancer biology.