Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2008) 16 OC2.5

ECE2008 Oral Communications Thyroid (9 abstracts)

Fetal cell microchimerism in papillary thyroid cancer: a possible role in tumor damage and tissue repair

Valentina Cirello 1 , Maria Paola Recalcati 2 , Marina Muzza 1 , Stefania Rossi 3 , Michela Perrino 1 , Paolo Beck-Peccoz 1 , Palma Finelli 2 & Laura Fugazzola 1


1Department of Medical Sciences and Endocrine Unit, University of Milan and Ospedale Maggiore IRCCS, Milan, Italy; 2Department of Biology and Genetics for Medical Sciences and Laboratory of Medical Cytogenetics and Molecular Genetics, University of Milan and Instituto Auxologico IRCCS, Milan, Italy; 3Pathology Unit, University of Milan & H San Paolo, Milano, Italy.

Fetal cells enter the maternal circulation during pregnancy and can persist in the maternal blood or tissues for decades, creating a physiological microchimerism. Since papillary thyroid cancer (PTC) is more frequent in female gender and it is the second more frequent tumor during pregnancy, the role of persisting microchimeric cells has been investigated. Tumour tissue specimens were obtained from 62 women with PTC, 41 of whom had at least one male child before the diagnosis of PTC. Male cells were identified by PCR ELISA studies on a male specific gene, the sex-determining region Y (SRY) and were further characterized by FISH. Male DNA was detected in the pathological tissue of the 17% of women who had a male pregnancy before the diagnosis. By FISH analyses, the total number of microchimeric male cells was significantly higher in neoplastic tissues than in normal sections. By immunoFISH, a technique combining FISH and immunohystochemistry in the same section, male cells expressing thyroglobulin were found in tumor and normal tissues, while male microchimeric cells stained with the CD45 common leukocyte antigen were detected only in pathological sections. Microchimeric cells negative for both markers were detected in tumour and in normal tissues, but they were significantly more frequent in tumoral samples.

In conclusion, the present study shows for the first time the presence of fetal cell microchimerism in women affected with PTC. CD45+ male cells found in the neoplastic tissues might be committed to destroy the tumoral cells, while Tg+ cells could have a repair function. Finally, microchimeric cells negative either for CD45 and for Tg could have staminal properties able to transdifferentiate in different cellular types. The whole of the results obtained suggests a protective role of microchimerism in thyroid cancer, though a possible role in carcinogenesis of persistent microchimeric cells cannot be excluded.

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