Expression pattern of RAGE and IGF-1 in the human fetal ovary and ovarian serous carcinoma (CROSBI ID 216244)
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Poljičanin, Ana ; Filipović, Natalija ; Vukušić Pušić, Tanja ; Šoljić, Violeta ; Čarić, Ana ; Saraga-Babić, Mirna ; Vukojević, Katarina
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Expression pattern of RAGE and IGF-1 in the human fetal ovary and ovarian serous carcinoma
The expression pattern of RAGE and IGF-1 proteins in different ovarian cell lineages was histologically analyzed in 6 fetal, 9 adult human ovaries, and 9 serous ovarian carcinomas (OSC) using immunohistochemical methods. Mild expression of IGF-1 in ovarian surface epithelium (Ose) and oocytes in the 15-week human ovaries increased to moderate or strong in the stromal cells, oocytes and follicular cells in week 22. Occasional mild RAGE expression was observed in Ose during week 15, while strong expression characterized primordial follicles in week 22. In the reproductive human ovary, IGF-1 was mildly to moderately expressed in all ovarian cell lineages except in theca cells of the tertiary follicle where IGF-1 was negative. RAGE was strongly positive in the granulosa cells and some theca cells of the tertiary follicle, while negative to mildly positive in all cells of the secondary follicle. In the postmenopausal human ovary IGF-1 and RAGE were mildly expressed in Ose and stroma. In OSC, cells were strongly positive to IGF-1 and RAGE, except for some negative stromal cells. Different levels of IGF-1 and RAGE co- expression characterized fetal ovarian cells during development. In reproductive ovaries, IGF-1 and RAGE were co-localized in the granulosa and theca interna cells of tertiary follicles, while in postmenopausal ovaries and OSC, IGF-1 and RAGE were co-localized in Ose and OSC cells respectively. Our results indicate that intracellular levels of IGF-1 and RAGE protein might regulate the final destiny of the ovarian cell populations prior and during folliculogenesis, possibly controlling the metastatic potential of OSC as well.
RAGE; IGF-1; Human fetus; Ovary; Serous ovarian carcinoma
S.I.: Immunomarkers in human developing and pediatric neoplastic tissues.
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