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Updated: May 23, 2025

An Orthotopic Mouse Model of Anaplastic Thyroid Carcinoma
Published on: April 17, 2013
Targeting Surface Markers in Anaplastic Thyroid Cancer: Future Directions in Ligand-bound Therapy
Janice Pakkianathan1, Samuel Chan1, Joseph Cruz1
1Division of Biochemistry, Center for Health Disparities & Molecular Medicine, Loma Linda University School of Medicine, Loma Linda, CA 92350, USA.
Abstract:
Anaplastic thyroid cancer (ATC) is the rarest and most aggressive form of thyroid cancer, known for its highly variable nature and poor prognosis, primarily due to the lack of effective treatments. While conventional therapies have had limited success, there remains an urgent need for novel therapeutic approaches to combat this disease. ATC tumors are resistant to the standard radioiodine therapy because they lack the sodium/iodide symporter (NIS), which is necessary for iodine uptake. However, recent advances in theranostics targeting cell surface markers have opened new avenues for treating ATC. We used the PubMed database and Google search engine to identify relevant articles using combinations of specific keywords related to the topic of interest, focusing on each surface marker. This review explores multiple surface markers identified in ATC and their promising roles for delivering therapeutic agents into tumors, inducing cell death. Several promising markers, including prostate-specific membrane antigen, vitamin D receptor, IGF-1 receptor, programmed death-ligand 1, epidermal growth factor receptor, and L-type amino acid transporter 1 (LAT-1), have been found in ATC and could serve as effective targets for delivering therapeutic agents to tumors, inducing cell death. Restoring NIS expression is also explored as a potential therapy for ATC. Additionally, boron neutron capture therapy, which utilizes LAT-1 expression, is highlighted as a future therapeutic option due to its ability to selectively target tumor cells while minimizing damage to surrounding healthy tissue. These strategies offer the potential to overcome many of the challenges associated with ATC, improving patient outcomes and overall survival.
Insights
Anaplastic thyroid cancer (ATC) is aggressive, lacking effective treatments. Targeting cell surface markers like LAT-1 offers new theranostic approaches for improved patient outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Theranostics
Background:
- Anaplastic thyroid cancer (ATC) is a rare, aggressive thyroid malignancy with a poor prognosis.
- Conventional therapies show limited efficacy due to ATC's resistance to radioiodine therapy, stemming from a lack of sodium/iodide symporter (NIS) expression.
Purpose of the Study:
- To review novel therapeutic strategies for anaplastic thyroid cancer by exploring cell surface markers as targets.
- To identify potential therapeutic agents and delivery mechanisms for improving ATC treatment outcomes.
Main Methods:
- Literature search of PubMed and Google Scholar using targeted keywords.
- Identification and analysis of relevant studies focusing on ATC surface markers and theranostic approaches.
Main Results:
- Several promising surface markers, including prostate-specific membrane antigen, vitamin D receptor, IGF-1 receptor, PD-L1, EGFR, and LAT-1, are identified in ATC.
- These markers show potential for targeted delivery of therapeutic agents to induce tumor cell death.
- Restoring NIS expression and Boron Neutron Capture Therapy (BNCT) utilizing LAT-1 are explored as future therapeutic avenues.
Conclusions:
- Targeting specific cell surface markers represents a promising strategy for developing effective anaplastic thyroid cancer therapies.
- Theranostic approaches and novel treatments like BNCT offer potential to overcome current treatment limitations and improve patient survival.
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