Related Experiment Video
Updated: Apr 4, 2026

Spontaneous Murine Model of Anaplastic Thyroid Cancer
Published on: February 3, 2023
A case of poorly differentiated thyroid carcinoma harboring an SMARCB1 mutation
Rika Sasaki1, Haruhiko Yamazaki2, Eita Kumagai3
1Department of Surgery, Yokohama City University School of Medicine, Yokohama, Kanagawa Japan.
None:
SWItch/sucrose non-fermentable (SWI/SNF) chromatin-remodeling complexes regulate nucleosome positioning. Its involvement has been suggested in anaplastic thyroid carcinoma and poorly differentiated thyroid carcinoma. We herein report an extremely rare case of poorly differentiated thyroid carcinoma harboring a mutation in SMARCB1, a subunit of the SWI/SNF complex. The patient was a 75‑year‑old woman with bilateral thyroid nodules who had been followed up for 27 years, with cytology classified as Bethesda II. The nodule enlarged rapidly to 7 cm, and computed tomography suggested airway invasion and multiple pulmonary nodules. An open biopsy of the thyroid mass was performed, and the lesion was diagnosed as poorly differentiated thyroid carcinoma. Lenvatinib therapy was initiated at the previous hospital, resulting in tumor shrinkage, and total thyroidectomy was performed 62 days after the initiation of treatment. Five months later, the patient was referred to our hospital for surgical management of pulmonary lesions. Left basal segmentectomy was performed, and histopathological examination confirmed metastasis from poorly differentiated thyroid carcinoma. Lung metastatic tissue was submitted to GenMineTOP, and an SMARCB1 mutation was detected. At the time of this report, 2 years and 7 months had passed since the initial surgery. Lenvatinib therapy was continued, and the disease remained stable. We report a case of poorly differentiated thyroid carcinoma with an SMARCB1 mutation. The accumulation of similar cases and additional immunohistochemical evaluations of past specimens may contribute to the development of targeted therapeutic strategies.
More Related Videos
Related Concept Videos
Loss of Tumor Suppressor Gene Functions
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
Loss of Tumor Suppressor Gene Functions
The Retinoblastoma Gene
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
Targeted Cancer Therapies
There are several types of targeted therapies against...
Cancer-Critical Genes II: Tumor Suppressor Genes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
Cancer-Critical Genes II: Tumor Suppressor Genes

