TY - JOUR
T1 - PAX8-PPARγ rearrangement in thyroid tumors
T2 - RT-PCR and immunohistochemical analyses
AU - Nikiforova, Marina N.
AU - Biddinger, Paul W.
AU - Caudill, Christy M.
AU - Kroll, Todd G.
AU - Nikiforov, Yuri E.
N1 - Copyright:
Copyright 2004 Elsevier Science B.V., Amsterdam. All rights reserved.
PY - 2002
Y1 - 2002
N2 - A PAX8-PPARγ rearrangement has been recently identified in follicular thyroid carcinomas, but not in follicular adenomas or other thyroid tumors. We report here the analyses of PAX8-PPARγ in a series of 118 thyroid tumors using a newly developed RT-PCR assay to detect this rearrangement in frozen and paraffin-embedded tissues and using immunostaining with a PPARγ antibody. PAX8-PPARγ was detected by RT-PCR in eight of 15 (53%) follicular carcinomas and two of 25 (8%) follicular adenomas but not in 35 papillary carcinomas (including 12 follicular variants), 12 Hurthle cell carcinomas, 12 Hurthle cell adenomas, two anaplastic carcinomas, one poorly differentiated carcinoma, or 16 hyperplastic nodules. The prevalence was higher in follicular carcinomas from patients with a history of radiation exposure (three of three). Strong, diffuse nuclear immunostaining with the PPARγ antibody correlated with the presence of PAX8-PPARγ detected by RT-PCR. Most sporadic follicular carcinomas positive for PAX8-PPARγ were overtly invasive, whereas tumors lacking the rearrangement were predominantly minimally invasive. The two follicular adenomas positive for PAX8-PPARγ had trabecular growth pattern and thick capsule, but no invasion, and thus may represent "pre-invasive" follicular carcinomas. The absence of PAX8-PPARγ rearrangements in Hurthle cell tumors and papillary thyroid carcinomas highlights the differences in the molecular pathogenesis of these thyroid tumors.
AB - A PAX8-PPARγ rearrangement has been recently identified in follicular thyroid carcinomas, but not in follicular adenomas or other thyroid tumors. We report here the analyses of PAX8-PPARγ in a series of 118 thyroid tumors using a newly developed RT-PCR assay to detect this rearrangement in frozen and paraffin-embedded tissues and using immunostaining with a PPARγ antibody. PAX8-PPARγ was detected by RT-PCR in eight of 15 (53%) follicular carcinomas and two of 25 (8%) follicular adenomas but not in 35 papillary carcinomas (including 12 follicular variants), 12 Hurthle cell carcinomas, 12 Hurthle cell adenomas, two anaplastic carcinomas, one poorly differentiated carcinoma, or 16 hyperplastic nodules. The prevalence was higher in follicular carcinomas from patients with a history of radiation exposure (three of three). Strong, diffuse nuclear immunostaining with the PPARγ antibody correlated with the presence of PAX8-PPARγ detected by RT-PCR. Most sporadic follicular carcinomas positive for PAX8-PPARγ were overtly invasive, whereas tumors lacking the rearrangement were predominantly minimally invasive. The two follicular adenomas positive for PAX8-PPARγ had trabecular growth pattern and thick capsule, but no invasion, and thus may represent "pre-invasive" follicular carcinomas. The absence of PAX8-PPARγ rearrangements in Hurthle cell tumors and papillary thyroid carcinomas highlights the differences in the molecular pathogenesis of these thyroid tumors.
KW - Chromosomal rearrangement
KW - Follicular carcinoma
KW - Immunohistochemistry
KW - PAX8-PPARγ
KW - Thyroid cancer
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U2 - 10.1097/00000478-200208000-00006
DO - 10.1097/00000478-200208000-00006
M3 - Article
C2 - 12170088
AN - SCOPUS:0035984201
SN - 0147-5185
VL - 26
SP - 1016
EP - 1023
JO - American Journal of Surgical Pathology
JF - American Journal of Surgical Pathology
IS - 8
ER -