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DOI 10.1007/s12022-006-0009-x

Медицинская библиотека · Endocrine pathology · 2006

Expression of prolactin receptor and prolactin in normal and malignant thyroid: a tissue microarray study.

Costa Patrícia, Catarino Ana Luísa, Silva Fernanda, Sobrinho Luís G, Bugalho Maria João

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

There is increasing evidence involving prolactin (PRL) and its receptor (PRLR) in the development of different cancers. The aim of the present study was to investigate the expression of PRLR and PRL in human thyroid tissues.

DESIGN AND

METHODS

Using tissue microarray (TMA) by immunohistochemical staining, we examined the expression level of PRLR and PRL in 314 specimens from 71 thyroid cancer patients and 15 normal thyroid samples.

RESULTS

Expression of the PRLR was observed in 93.3% of normal thyroid samples and in 76.1% of all thyroid cancers, while expression of PRL was observed in only 10% of medullary thyroid carcinomas and not at all in the other specimens, whether normal or neoplastic. Moreover, results suggested an overexpression of PRLR in 70% of medullary thyroid carcinomas, whereas 53.3% of poorly differentiated thyroid carcinomas showed a negative pattern of staining (p = 0.014 vs normal).

CONCLUSIONS

Present data revealed, for the first time, a widespread expression of PRLR in normal and neoplastic human thyroid tissues as well as a scarce expression of PRL, observed only in a few medullary thyroid carcinomas. Whether the overexpression of PRLR observed in medullary thyroid carcinomas or the underexpression of PRLR observed in poorly differentiated thyroid carcinomas play a contributory role in the oncogenesis of these tumors remains to be determined.

Для цитирования: Costa Patrícia, Catarino Ana Luísa, Silva Fernanda, Sobrinho Luís G, Bugalho Maria João. Expression of prolactin receptor and prolactin in normal and malignant thyroid: a tissue microarray study.. Endocrine pathology. 2006. DOI: 10.1007/s12022-006-0009-x.

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