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HOXD9 prioritization within developmental regulator-related genes suggests stage-adjusted prognostic relevance in hepatocellular carcinoma

  
@article{TCR120229,
	author = {Junling Zhu and Xujie Tang and Qianru Zhu and Sen Jiang},
	title = {HOXD9 prioritization within developmental regulator-related genes suggests stage-adjusted prognostic relevance in hepatocellular carcinoma},
	journal = {Translational Cancer Research},
	volume = {15},
	number = {7},
	year = {2026},
	keywords = {},
	abstract = {Background: Prognostic stratification in hepatocellular carcinoma (HCC) remains difficult because standard staging systems do not fully capture the biological heterogeneity of the disease. We hypothesized that developmental regulators could provide a biologically relevant framework for prioritizing prognostic markers.Methods: RNA sequencing (RNA-seq) and clinical data from The Cancer Genome Atlas liver hepatocellular carcinoma (TCGA-LIHC) cohort were analyzed. Tumor vs. normal differential expression analysis was performed using differential expression analysis for sequence count data 2 (DESeq2). Developmental regulator-related candidate genes were prioritized through a stepwise framework integrating differential expression, clinicopathological association, Kaplan-Meier survival analysis, and Cox regression. A main prognostic model was constructed from the final independent factors and evaluated using a nomogram, calibration analysis, and time-dependent receiver operating characteristic (ROC) analysis. The incremental prognostic value of HOXD9 beyond pathologic stage was assessed using the likelihood ratio test, Harrell’s concordance index (C-index), bootstrap-based delta C-index analysis, and time-dependent area under the curve (AUC) comparison. External validation was performed in the LIRI-JP (Liver Cancer-RIKEN, Japan) cohort.Results: Among the screened developmental regulator-related genes, HOXD9 and MESP2 showed the most consistent signals across differential expression, clinicopathological association, and survival analyses. In multivariable Cox regression in the TCGA-LIHC cohort, only pathologic stage [hazard ratio (HR) =1.565, 95% confidence interval (CI): 1.266–1.935; P},
	issn = {2219-6803},	url = {https://tcr.amegroups.org/article/view/120229}
}