fig2

CDK4/6 and BET inhibitors synergistically suppress pancreatic tumor growth and epithelial-to-mesenchymal transition by regulating the GSK3β-mediated Wnt/β-catenin pathway

Figure 2. Establishment and evaluation of a CDK4/6-based nomogram in PDAC cohorts. (A) Nomogram parameters, including gender, age, tumor size, diabetes, CA199 level, lymphatic metastasis, tumor differentiation, perineural invasion, tumor embolus, distant metastasis, TNM stage, and CDK4/6 expression, were used to predict 1-, 2- and 3-year survival in PDAC patients; (B and C) Time-dependent ROC curves comparing the nomogram, clinical parameters, and TNM stage in the training and validation cohorts. CDK4/6: Cyclin-dependent kinases 4 and 6; PDAC: pancreatic ductal adenocarcinoma; TNM: tumor size, node, and metastasis; ROC: receiver operating characteristic.

Cancer Drug Resistance
ISSN 2578-532X (Online)

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