4.7 Article

Glycolysis related gene expression signature in predicting prognosis of laryngeal squamous cell carcinoma

Journal

BIOENGINEERED
Volume 12, Issue 1, Pages 8738-8752

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/21655979.2021.1980177

Keywords

Laryngeal squamous cell carcinoma; TCGA; GEO; prognosis; gene signature

Funding

  1. National Natural Science Foundation of China [81972529]
  2. Science and Technology Commission of Shanghai Municipality [19411961300]

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Research identified and validated two novel glycolytic gene signatures, DDIT4 and PLOD2, as potential independent risk factors for predicting overall survival in laryngeal squamous cell carcinoma (LSCC). These findings may provide a therapeutic target and survival prediction marker for LSCC patients.
Researches have suggested that aerobic glycolysis can reflect the development and progression of most carcinomas. We aimed to investigate whether glycolysis-related genes (GRGs) are associated with overall survival in laryngeal squamous cell carcinoma (LSCC). Here, we identified differentially expressed GRGs in TCGA dataset and microarray sample of GSE27020 from GEO database. A set of two glycolytic gene signatures, including DDIT4 and PLOD2 was screened through Cox and Lasso regression. The risk score was calculated using the gene expression of the two GRGs. The high-risk group presented a poor prognosis through Kaplan-Meier method. The ROC curve indicated good prediction performance in survival based on the validation of four cohorts. Univariate and multivariate Cox regression analyses suggested that two-gene signature could be an independent risk factor in LSCC. A total of 17 LSCC patients were enrolled to clarify the genetic expression through using reverse transcription-polymerase chain reaction (RT-PCR). A visualized nomogram was then constructed to predict 1-, 3-, and 5-year overall survival. Taken together, two novel glycolytic gene signatures were discovered and validated, providing a potential therapeutic and overall survival (OS)-prediction biomarker for LSCC.

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