Abstract

BackgroundColon cancer is one of the leading causes of cancer deaths in the USA and around the world. Molecular level characters, such as gene expression levels and mutations, may provide profound information for precision treatment apart from pathological indicators. Transcription factors function as critical regulators in all aspects of cell life, but transcription factors-based biomarkers for colon cancer prognosis were still rare and necessary.MethodsWe implemented an innovative process to select the transcription factors variables and evaluate the prognostic prediction power by combining the Cox PH model with the random forest algorithm. We picked five top-ranked transcription factors and built a prediction model by using Cox PH regression. Using Kaplan-Meier analysis, we validated our predictive model on four independent publicly available datasets (GSE39582, GSE17536, GSE37892, and GSE17537) from the GEO database, consisting of 925 colon cancer patients.ResultsA five-transcription-factors based predictive model for colon cancer prognosis has been developed by using TCGA colon cancer patient data. Five transcription factors identified for the predictive model is HOXC9, ZNF556, HEYL, HOXC4 and HOXC6. The prediction power of the model is validated with four GEO datasets consisting of 1584 patient samples. Kaplan-Meier curve and log-rank tests were conducted on both training and validation datasets, the difference of overall survival time between predicted low and high-risk groups can be clearly observed. Gene set enrichment analysis was performed to further investigate the difference between low and high-risk groups in the gene pathway level. The biological meaning was interpreted. Overall, our results prove our prediction model has a strong prediction power on colon cancer prognosis.ConclusionsTranscription factors can be used to construct colon cancer prognostic signatures with strong prediction power. The variable selection process used in this study has the potential to be implemented in the prognostic signature discovery of other cancer types. Our five TF-based predictive model would help with understanding the hidden relationship between colon cancer patient survival and transcription factor activities. It will also provide more insights into the precision treatment of colon cancer patients from a genomic information perspective.

Highlights

  • Colon cancer is one of the leading causes of cancer deaths in the USA and around the world

  • The goal of our study is to identify the fundamental transcript factors, which are associated with clinical outcomes of colon cancer patients, by implementing an innovative cancer prognosis signature discovery process that combines the random forest algorithm with classic Cox Proportional Hazard (Cox Cox proportional hazard (PH)) method

  • The univariate Cox PH regression was applied to the gene expression profiles for the overlapping 1780 Transcription factor (TF) and the patient clinical data in The Cancer Genome Atlas (TCGA) colon cohort, to identify the TFs, which are associated with the survival of the patients and have the potential using as prognostic markers

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Summary

Introduction

Colon cancer is one of the leading causes of cancer deaths in the USA and around the world. Molecular level characters, such as gene expression levels and mutations, may provide profound information for precision treatment apart from pathological indicators. Colon cancer is the sixth in men and the fifth in women the most common cause of cancer-related death globally [1]. Colon cancer is a complex disease with many risk factors, such as genetics, lifestyles, and dietary habits. Among them, inherited gene mutation, which can pass through family members, is one critical factor to increase one’s colon cancer risk. Colon cancer treatments should be tailored based on the individual’s risk factors and genetic factors

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