Cribriform morular thyroid carcinoma: Clinicopathological and molecular basis for both a preventive and therapeutic approach for a rare tumor (Review)

• Published in: Oncology reports Vol. 52; no. 3; p. 1
• Main Authors: Cameselle-García, Soledad, Abdulkader-Nallib, Ihab, Sánchez-Ares, María, Cameselle-Teijeiro, José Manuel
• Format: Journal Article
• Language: English
• Published: Greece Spandidos Publications 01.09.2024; Spandidos Publications UK Ltd; D.A. Spandidos
• Subjects: Adenomatous Polyposis Coli - genetics; Adenomatous Polyposis Coli - pathology; Adjuvant treatment; beta Catenin - genetics; beta Catenin - metabolism; Cancer; Carcinoma; Colorectal cancer; Estrogen; Estrogens; Female; Gene mutations; Genes; Genetic disorders; Health aspects; Humans; Metastasis; Mortality; Mutation; Polyps; Progesterone; Review; Spain; Telomerase; Thyroid cancer; Thyroid diseases; Thyroid Neoplasms - genetics; Thyroid Neoplasms - pathology; Transcription factors; Tumor proteins; Tumors; Wnt Signaling Pathway; Spain; United States > US; cribriform morular thyroid carcinoma; Wnt/β‑catenin signaling pathway; APC; familial adenomatous polyposis; estrogen receptors; β‑catenin
• ISSN: 1021-335X; 1791-2431; 1791-2431
• DOI: 10.3892/or.2024.8778

Cribriform morular thyroid carcinoma (CMTC) has been included within the group of thyroid tumors of uncertain histogenesis in the recent World Health Organization classification of endocrine tumors. Most CMTCs occur in young euthyroid women with multiple (and bilateral) thyroid nodules in cases associated with familial adenomatous polyposis (FAP) or as single nodules in sporadic cases. CMTC generally behaves indolently, while aggressiveness and mortality are associated with high‑grade CMTC. This tumor histologically displays a distinctive combination of growth patterns with morular structures. Strong diffuse nuclear and cytoplasmic immunostaining for β‑catenin is the hallmark of CMTC. Tumor cells are also positive for thyroid transcription factor‑1 and for estrogen and progesterone receptors, but negative for thyroglobulin and calcitonin. It is possible that the CMTC phenotype could result from blockage in the terminal/follicular differentiation of follicular cells (or their precursor cells) secondary to the permanent activation of the Wnt/β‑catenin pathway. In CMTC, the activation of the Wnt/β‑catenin pathway is the central pathogenetic event, which in FAP‑associated cases results from germline mutations of the APC regulator of WNT signaling pathway ( ) gene, and in sporadic cases from somatic inactivating mutations in the and genes. Estrogens appear to play a tumor‑promoting role by stimulating both the PI3K/AKT/mTOR and the RAS/RAF/MAPK signaling pathways. Additional somatic mutations (i.e. RET rearrangements, or KRAS, phosphatidylinositol‑4,5‑bisphosphate 3‑kinase catalytic subunit α, telomerase reverse transcriptase or tumor protein 53 mutations) may further potentiate the development and progression of CMTC. While hemithyroidectomy would be the treatment of choice for sporadic cases without high‑risk data, total thyroidectomy would be indicated in FAP‑associated cases. There is insufficient clinical data to propose therapies targeting the Wnt/β‑catenin pathway, but multikinase or selective inhibitors could be used in a manner analogous to that of conventional thyroid tumors. It is also unknown whether adjuvant antiestrogenic therapy could be useful in the subgroup of women undergoing surgery with high‑risk CMTC, as well as when there is tumor recurrence and/or metastasis.