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Published on: August 23, 2019
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.
Abstract:
Medullary thyroid cancer (MTC) is a rare malignancy that arises from calcitonin-producing C-cells. Curative treatment for patients with metastatic MTC is challenging. Identifying the mechanisms by which cancer cells inhibit the activity of immune cells provides an opportunity to develop new therapies that restore anticancer activity. Little is known about the immunological phenomena underlying MTC. Here, we examined the expression profile of 395 genes associated with MTC. The study included 51 patients diagnosed with MTC at a single center. Bioinformatical analysis revealed that CD276 expression in MTC cells was at least three-fold higher than that in normal tissue. The expression of CD276 showed a weak but statistically significant positive correlation with tumor diameter, but we did not find a significant association between CD276 expression and other histopathological clinical factors, or the response to initial therapy. A search of published data identified the monoclonal antibody (inhibitor) enoblituzumab as a potential drug for patients diagnosed with MTC overexpressing CD276.
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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