
Oncotarget
Gene Alterations in Thyroid Cancer Mediate Resistance to BRAF Inhibition & Anaplastic Transformation
Jan 29, 2024
In this podcast, researchers Mark Lee and Luc GT Morris discuss genetic alterations in thyroid cancer that mediate resistance to BRAF inhibition and anaplastic transformation. They explore the limited response to standard therapy in advanced-stage thyroid cancers. They also talk about the potential efficacy of dual-target therapies and the combination of targeted therapy with immunotherapy.
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Quick takeaways
- Thyroid tumors with the BRAF V600E mutation show resistance to BRAF inhibitors and can transition to an alternative cell state, leading to tumor dedifferentiation.
- Genetic alterations in pathways such as PI3K/AKT/MTOR, MAP/ERK, MET, NF2, NRAS, RAZA1, SWI/SNF chromatin remodeling complex, ARID2, PBRM1, and JAK/STAP contribute to resistance to BRAF blockade and may drive tumor dedifferentiation in thyroid cancer.
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Resistance mechanisms in thyroid cancer
Some thyroid cancers exhibit resistance to standard therapy and limited response to BRAF inhibitors. The BRAF V600E mutation is often found in these tumors, but their response to BRAF inhibitors is short-lived due to compensatory resistance mechanisms. Resistance can occur through the transition to an alternative cell state, leading to tumor de-differentiation. Non-genetic alterations in various pathways such as PI3K/AKT/MTOR, MAP/ERK, MET, NF2, NRAS, RAZA1, SWI/SNF chromatin remodeling complex, ARID2, PBRM1, and JAK/STAP contribute to resistance to BRAF blockade and may drive tumor de-differentiation.
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