The immunotherapy candidate TNFSF4 may help the induction of a promising immunological response in breast carcinomas

Kai Li1,2, Lei Ma3, Ye Sun4

  • 1Department of Thoracic Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, 277 Yanta West Road, Xi'an, 710061, Shaanxi, China.

Scientific Reports
|September 21, 2021
PubMed

Insights

Immune checkpoint blockade shows promise for breast cancer treatment. Targeting Tumor Necrosis Factor Superfamily Member 4 (TNFSF4) may enhance antitumor immunity and improve outcomes across breast cancer subtypes.

Area of Science:

  • Oncology
  • Immunotherapy
  • Molecular Biology

Background:

  • Immune checkpoint blockade (ICB) has improved survival in systemic malignancies.
  • Its efficacy in breast cancer remains largely undetermined.
  • Identifying predictive biomarkers for ICB in breast cancer is crucial.

Purpose of the Study:

  • To explore factors influencing immunotherapy outcomes in breast cancer.
  • To identify and validate potential therapeutic targets for breast cancer immunotherapy.
  • To investigate the role of Tumor Necrosis Factor Superfamily Member 4 (TNFSF4) in breast cancer immunity.

Main Methods:

  • Analysis of public databases for gene expression and survival data.
  • Selection of TNFSF4 based on expression, survival association, and immune prediction.
  • In silico validation of TNFSF4 interactions with immune molecules and T cell signatures.

Main Results:

  • TNFSF4 exhibits oncogenic features in breast carcinoma.
  • TNFSF4 expression is linked to antitumor immunity induction and T cell responses, independent of endocrine status.
  • TNFSF4 blockade demonstrates potential in targeting cancer stem cells, suggesting therapeutic efficacy.

Conclusions:

  • TNFSF4 is a novel target for breast cancer immunotherapy.
  • TNFSF4 blockade may offer a new therapeutic strategy with broad applicability across breast cancer subtypes.
  • This study provides a potential tool for enhancing long-term effectiveness in breast cancer treatment.

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