M. Patey et al., Immunohistochemical study of thrombospondin and its receptors alpha root beta 3 and CD36 in normal thyroid and in thyroid tumours, J CLIN PATH, 52(12), 1999, pp. 895-900
Citations number
42
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Aim-To describe the pattern of distribution of thrombospondin (TSP1) and it
s receptors, alpha root beta 3 integrin and CD36, in normal human thyroid t
issue and to compare their expression in different benign and malignant thy
roid conditions.
Methods-Immunohistochemistry was used to study TSP1 and its receptors in 40
surgical thyroidectomy specimens (normal parenchyma, 7; follicular adenoma
, 4; multinodular goitre, 13; papillary carcinoma, 6; follicular carcinoma,
8; anaplastic carcinoma, 2).
Results-In the normal thyroid parenchyma, there was weak expression of TSP1
limited to the vessels with no staining of the extracellular matrix. In go
itres, the expression of TSP1 was more pronounced in areas of fibrosis, wit
h staining of alpha root beta 3 on thyrocytes located in the vicinity. In t
hyroid adenomas, expression of TSP1 was slightly enhanced compared with nor
mal tissue, located in the basement membrane of vessels. In papillary carci
nomas, TSP1 was abundant in the desmoplastic stroma with a cytoplasmic dist
ribution of alpha root beta 3 integrin in thyrocytes. In follicular carcino
mas, TSP1 was less abundant in the extracellular matrix, limited to the ves
sels of the stroma with a weaker expression of alpha root beta 3 on thyrocy
tes than in papillary carcinomas. In anaplastic carcinomas, TSP1 was only p
resent in the numerous capillaries of the stroma, with a marked positivity
for alpha root beta 3 in one case. No immunostaining of thyrocytes is obser
ved with CD36.
Conclusions-These results suggest the importance of the interaction between
alpha root beta 3 integrin and TSP1 during remodelling of the matrix in fi
brous goitres with areas of early sclerosis comparable with wound healing.
In papillary carcinomas, the overexpression of TSP1 restricted to the strom
a suggests protective effects against tumour progression.