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Updated: Apr 21, 2026

Spontaneous Murine Model of Anaplastic Thyroid Cancer
Published on: February 3, 2023
Personalized therapy in patients with anaplastic thyroid cancer: targeting genetic and epigenetic alterations
1Laboratory of Human Thyroid Cancers Preclinical and Translational Research, Division of Cancer Biology and Angiogenesis, Department of Pathology, Center for Vascular Biology Research, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, Massachusetts 02215.
Context:
Anaplastic thyroid cancer (ATC) is the most lethal of all thyroid cancers and one of the most aggressive human carcinomas. In the search for effective treatment options, research toward targeted, personalized therapies is proving to be a path with great potential. As we gain a deeper understanding of the genetic (eg, BRAF(V600E), PIK3CA, TP53, hTERT mutations, etc) and epigenetic (eg, histone methylation, histone de-acetylation, microRNA regulatory circuits, etc) alterations driving ATC, we are able to find targets when developing novel therapies to improve the lives of patients. Beyond development, we can look into the effectiveness of already approved targeted therapies (eg, anti-BRAF(V600E) selective inhibitors, tyrosine kinase inhibitors, histone deacetylase inhibitors, inhibitors of DNA methylation, etc) to potentially test in ATC after learning the molecular mechanisms that aid in tumor progression.
Design:
We performed a literature analysis in Medline through the PubMed web site for studies published between 2003 and 2014 using the following main keywords: anaplastic thyroid cancer, genetic and epigenetic alterations.
Objective:
Here, we outlined the common pathways that are altered in ATC, including the BRAF(V600E)/ERK1/2-MEK1/2 and PI3K-AKT pathways. We then examined the current research looking into personalized, potential targeted therapies in ATC, mentioning those that have been tentatively advanced into clinical trials and those with the potential to reach that stage. We also reviewed side effects of the current and potential targeted therapies used in patients with advanced thyroid cancer.
Conclusions:
DNA and RNA next-generation sequencing analysis will be fundamental to unraveling a precise medicine and therapy in patients with ATC. Indeed, given the deep biological heterogeneity/complexity and high histological grade of this malignancy and its tumor microenvironment, personalized therapeutic approaches possibly based on the use of combinatorial targeted therapy will provide a rational approach when finding the optimal way to improve treatments for patients with ATC.
Insights
Anaplastic thyroid cancer (ATC) research focuses on genetic and epigenetic alterations to develop personalized targeted therapies. Understanding these molecular drivers is key to improving treatment strategies for this aggressive cancer.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Anaplastic thyroid cancer (ATC) is a highly lethal and aggressive carcinoma.
- Understanding genetic (e.g., BRAF(V600E), PIK3CA) and epigenetic alterations is crucial for developing targeted therapies.
- Research explores personalized medicine approaches for ATC treatment.
Purpose of the Study:
- To outline common altered pathways in ATC, including BRAF/ERK and PI3K-AKT.
- To examine current research on personalized targeted therapies for ATC.
- To review potential and current targeted therapies and their side effects.
Main Methods:
- Literature analysis of Medline via PubMed (2003-2014).
- Keywords: anaplastic thyroid cancer, genetic and epigenetic alterations.
- Review of common molecular pathways and targeted therapies.
Main Results:
- Identified BRAF(V600E)/ERK1/2-MEK1/2 and PI3K-AKT as commonly altered pathways.
- Examined targeted therapies, including those in clinical trials and with future potential.
- Reviewed side effects of current and potential targeted therapies for advanced thyroid cancer.
Conclusions:
- Next-generation sequencing (DNA and RNA) is fundamental for precise medicine in ATC.
- Personalized therapeutic approaches, potentially using combinatorial targeted therapy, are rational for improving ATC treatment.
- Addressing the biological heterogeneity and complexity of ATC is essential for effective therapy.
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