@article{4026,
  author = {Haonan Song and Haoyuan Jiang and Weichu Hu and Yan Hai and Yihuan Cai and Hu Li and Yuru Liao and Yi Huang and Xiaogang Lv and Yefei Zhang and Jiping Zhang and Yan Huang and Xiaomei Liang and Hao Huang and Xinhua Lin and Yifeng Wang and Xiao Yi},
  title = {Cervical extracellular matrix hydrogel optimizes tumor heterogeneity of cervical squamous cell carcinoma organoids},
  abstract = {Cervical cancer, primarily squamous cell carcinoma, is the most prevalent gynecologic malignancy. Organoids can mimic tumor development in vitro, but current Matrigel inaccurately replicates the tissue-specific microenvironment. This limitation compromises the accurate representation of tumor heterogeneity. We collected para-cancerous cervical tissues from patients diagnosed with cervical squamous cell carcinoma (CSCC) and prepared uterine cervix extracellular matrix (UCEM) hydrogels. Proteomic analysis of UCEM identified several tissue-specific signaling pathways including human papillomavirus, phosphatidylinositol 3-kinase–AKT, and extracellular matrix receptor. Secreted proteins like FLNA, MYH9, HSPA8, and EEF1A1 were present, indicating UCEM successfully maintained cervical proteins. UCEM provided a tailored microenvironment for CSCC organoids, enabling formation and growth while preserving tumorigenic potential. RNA sequencing showed UCEM-organoids exhibited greater similarity to native CSCC and reflected tumor heterogeneity by exhibiting CSCC-associated signaling pathways including virus protein-cytokine, nuclear factor κB, tumor necrosis factor, and oncogenes EGR1, FPR1, and IFI6. Moreover, UCEM-organoids developed chemotherapy resistance. Our research provides insights into advanced organoid technology through native matrix hydrogels.},
  year = {2024},
  journal = {Science Advances},
  volume = {10},
  pages = {eadl3511},
  month = {2024-05-15},
  url = {https://www.science.org/doi/10.1126/sciadv.adl3511},
  doi = {10.1126/sciadv.adl3511},
}