Identification of Nephrogenic Therapeutic Biomarkers of Wilms Tumor Using Machine Learning

Hanxiang Liu1, Chaozhi Tang2, Yi Yang1

  • 1Pediatric Urology, Shengjing Hospital of China Medical University, Shenyang 110001, China.

Journal of Oncology
|August 23, 2021
PubMed

Insights

Researchers identified eight key genes in Wilms tumor, developing a risk model to predict prognosis. This discovery aids in personalized treatment strategies for pediatric kidney cancer, improving outcomes for high-risk patients.

Area of Science:

  • Pediatric Oncology
  • Molecular Biology
  • Genomics

Background:

  • Wilms tumor is the leading childhood kidney cancer, with over 90% survival.
  • Certain subgroups, like those with bilateral or recurrent disease, have poorer outcomes.
  • Identifying novel biomarkers and therapies is crucial for improving treatment efficacy.

Purpose of the Study:

  • To identify novel, renal-specific, differentially expressed genes in Wilms tumors.
  • To develop a prognostic risk model for predicting patient outcomes.
  • To explore potential therapeutic strategies based on identified gene signatures.

Main Methods:

  • Utilized Therapeutically Applicable Research to Generate Effective Treatments (TREATS) and Gene Expression Omnibus (GEO) RNA microarray datasets.
  • Identified eight differentially expressed genes in Wilms tumors from 33 adult tumor samples.
  • Constructed a risk model using survival forest and multivariate Cox regression analysis.

Main Results:

  • Eight differentially expressed genes were identified as renal-specific in Wilms tumors.
  • The developed risk model effectively predicts prognosis, with the risk score being an independent prognostic factor.
  • High-risk patients showed increased sensitivity to immunotherapy and chemotherapy.

Conclusions:

  • The identified gene signature and risk model offer valuable tools for prognostic prediction in Wilms tumor.
  • Findings suggest potential for developing personalized and precise treatment strategies.
  • Further research into these genes may uncover new therapeutic targets for challenging Wilms tumor cases.

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