A Hypoxia Molecular Signature-Based Prognostic Model for Endometrial Cancer Patients.
Yang JiaoRui GengZihang ZhongSenmiao NiWen LiuZhiqiang HeShilin GanQinghao HuangJinHui LiuJianling BaiPublished in: International journal of molecular sciences (2023)
Endometrial cancer has the highest incidence of uterine corpus cancer, the sixth most typical cancer in women until 2020. High recurrence rate and frequent adverse events were reported in either standard chemotherapy or combined therapy. Hence, developing precise diagnostic and prognostic approaches for endometrial cancer was on demand. Four hypoxia-related genes were screened for the EC prognostic model by the univariate, LASSO, and multivariate Cox regression analysis from the TCGA dataset. QT-PCR and functional annotation analysis were performed. Associations between predicted risk and immunotherapy and chemotherapy responses were investigated by evaluating expressions of immune checkpoint inhibitors, infiltrated immune cells, m6a regulators, and drug sensitivity. The ROC curve and calibration plot indicated a fair predictability of our prognostic nomogram model. NR3C1 amplification, along with IL-6 and SRPX suppressions, were detected in tumor. High stromal score and enriched infiltrated aDCs and B cells in the high-risk group supported the hypothesis of immune-deserted tumor. Hypoxia-related molecular subtypes of EC were then identified via the gene signature. Cluster 2 patients showed a significant sensitivity to Vinblastine. In summary, our hypoxia signature model accurately predicted the survival outcome of EC patients and assessed translational and transcriptional dysregulations to explore targets for precise medical treatment.
Keyphrases
- endometrial cancer
- end stage renal disease
- newly diagnosed
- chronic kidney disease
- peritoneal dialysis
- endothelial cells
- gene expression
- healthcare
- emergency department
- squamous cell carcinoma
- type diabetes
- stem cells
- single molecule
- papillary thyroid
- genome wide
- risk factors
- polycystic ovary syndrome
- high resolution
- skeletal muscle
- locally advanced
- mesenchymal stem cells
- patient reported
- atomic force microscopy
- replacement therapy
- genome wide identification