SCIENTIFIC EVIDENCE

Fatty acid oxidation drives acetyl-CoA-dependent H3K9ac reprogramming to promote adaptive resistance to BRAF V600E inhibition in thyroid cancer.

Cell death & disease
Wang X, Zhang J, Yuan J, Wen L, Ying T, Xu Z, Zhou Z, Chen S, Zhou Q, Sheng J, Luo C, Teng L, Wang W.

Publication Overview

Key findings, Countstar context, and access to the original paper.
2026
3D Culture
Cancer Research
Organoid Culture
Key Finding
In addition, higher expression of RUNX1 correlates with poorer prognosis in thyroid cancer. The work reveals a metabolic-epigenetic axis underlying adaptive response to BRAFi and identifies RUNX1 as a novel oncogene in thyroid cancer.
Countstar Connection
Cell viability was assessed in the study samples with Countstar Castor S1 within the organoid or 3D-culture workflow.
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