Personalized therapy in patients with anaplastic thyroid cancer: targeting genetic and epigenetic alterations

Neal Smith1, Carmelo Nucera

  • 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.

Abstract

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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