Pregled bibliografske jedinice broj: 740111
Immunohistochemical expression of SFRP1 and SFRP3 proteins in normal and malignant reproductive tissues of rats and humans
Immunohistochemical expression of SFRP1 and SFRP3 proteins in normal and malignant reproductive tissues of rats and humans // Applied immunohistochemistry & molecular morphology, 22 (2014), 9; 681-687 doi:10.1097/PAI.0000000000000019 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 740111 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Immunohistochemical expression of SFRP1 and SFRP3
proteins in normal and malignant reproductive tissues
of rats and humans
Autori
Partl Zmijanac, Jasenka ; Fabijanović, Dora ; Škrtić, Anita ; Vranić, Semir ; Nikuševa Martić, Tamara ; Šerman, Ljiljana
Izvornik
Applied immunohistochemistry & molecular morphology (1541-2016) 22
(2014), 9;
681-687
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
SFRP1 ; SFRP3 ; rat ; placenta
Sažetak
Secreted frizzled-related proteins 1 and 3 (SFRP1 and SFRP3) act as Wnt signaling pathway antagonists and play an important role in embryonic development and carcinogenesis. The aim of the present study was to analyze immunohistochemically the distribution of 2 SFRP family proteins, SFRP1 and SFRP3, in an experimental rat model, in normal and intrauterine growth-restricted (IUGR) human placentas, and in a subset of the corresponding human trophoblastic tumors (pure choriocarcinomas and mixed germ cell tumors with choriocarcinoma component). In rats, expression of both SFRP1 and SFRP3 was pronounced in the perimetrium and myometrium, whereas decidual cells showed only occasional positive cytoplasmic staining. The most prominent expression of both proteins was found in blood vessel endothelial cells. Stereological variable of volume density (Vv, mm) showed statistically higher expression of SFRP1 and SFRP3 in human IUGR placentas than in normal pregnancy placentas (P<0.0001). Compared with adjacent normal/benign tissues, reduced expression of SFRP1 and SFRP3 was observed in human trophoblastic tumors (58.5% and 31.25%, respectively), although none of the examined tumors exhibited complete loss of either protein. Our study indicates that increased expression of both SFRP1 and SFRP3 may contribute to the pathogenesis of IUGR placental dysfunction, whereas the loss of these proteins may be involved in the development of human trophoblastic tumors.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb
Profili:
Anita Škrtić
(autor)
Ljiljana Šerman
(autor)
Tamara Nikuševa Martić
(autor)
Jasenka Zmijanac Partl
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE