Molecular analysis of minimally invasive follicular carcinomas by gene profiling

Carrie C. Lubitz, Lisa A. Gallagher, David J. Finley, Baixin Zhu, Thomas J. Fahey, Bhuvanesh Singh, John M. Monchik, Martha A. Zeiger, Electron Kebebew

Research output: Contribution to journalArticlepeer-review

33 Scopus citations


Background. While the majority of minimally invasive follicular thyroid carcinoma (MIFTC) behave like follicular adenomas, some recur or metastasize. These studies were conducted to determine if molecular profiling can enhance our understanding of MIFTC and to perhaps offer a better classification schema. Methods. Microarray analysis was performed on 27 follicular neoplasms. Thirteen follicular adenomas (FAs) were compared with 7 widely invasive follicular thyroid carcinomas (WIFTCs) to generate a list of differentially expressed genes. Next, 7 MIFTCs were analyzed along with the other samples in a cluster analysis. The MIFTCs were then compared directly against both the adenoma and WIFTC groups to investigate genetic relatedness. Results. FAs and WIFTCs have distinct genetic profiles, with 401 differentially expressed genes. The 7 MIFTCs were added to the analysis. Six of 7 of the MIFTCs were grouped with the adenomas, 4 of which created their own subgroup. When analyzed directly, MIFTCs had 223 differently expressed genes, compared with FAs, and 365, compared with WIFTCs. Conclusions. Molecular profiling illustrates that the majority of MIFTCs comprise a subclass of follicular neoplasms, and, while most MIFTCs are genetically similar to adenomas, our patient data suggest that these tumors may deserve greater suspicion of malignant potential. Gene profiling can provide insight into the molecular pathogenesis of MIFTC.

Original languageEnglish (US)
Pages (from-to)1042-1049
Number of pages8
Issue number6
StatePublished - Dec 2005

ASJC Scopus subject areas

  • Surgery


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