Immune Profiling of Medullary Thyroid Cancer-An Opportunity for Immunotherapy

Kinga Hińcza-Nowak1,2, Artur Kowalik1,3, Agnieszka Walczyk2,4

  • 1Department of Molecular Diagnostics, Holycross Cancer Centre, 25-734 Kielce, Poland.

Genes
|October 23, 2021
PubMed

Insights

Medullary thyroid cancer (MTC) cells show significantly higher CD276 expression. This finding suggests enoblituzumab as a potential therapy for MTC patients overexpressing this immune-inhibiting marker.

Area of Science:

  • Oncology
  • Immunology
  • Genetics

Background:

  • Medullary thyroid cancer (MTC) is a rare cancer originating from C-cells, posing treatment challenges, especially in metastatic cases.
  • Understanding immune cell inhibition mechanisms in MTC is crucial for developing novel therapeutic strategies.
  • The immunological landscape of MTC remains largely unexplored.

Purpose of the Study:

  • To investigate the gene expression profile of medullary thyroid cancer.
  • To identify potential therapeutic targets by examining immune cell interactions in MTC.
  • To explore the role of CD276 in MTC pathogenesis and its correlation with clinical factors.

Main Methods:

  • Analysis of gene expression profiles for 395 genes in 51 MTC patients.
  • Bioinformatic analysis to compare gene expression in MTC versus normal tissue.
  • Correlation analysis between CD276 expression and clinical/histopathological factors.

Main Results:

  • CD276 expression was found to be at least three-fold higher in MTC cells compared to normal tissue.
  • A weak but significant positive correlation was observed between CD276 expression and tumor diameter.
  • No significant association was found between CD276 levels and other clinical factors or treatment response.

Conclusions:

  • Elevated CD276 expression in MTC suggests its potential role in immune evasion.
  • The monoclonal antibody enoblituzumab is identified as a potential therapeutic agent for MTC patients with high CD276 expression.
  • Further research into CD276's function could lead to targeted immunotherapies for medullary thyroid cancer.

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