@article{2995261, title = "Insulin-like growth factor-1 isoform mRNA expression in women with endometriosis: Eutopic endometrium versus endometriotic cyst", author = "Milingos, D. and Katopodis, H. and Milingos, S. and Protopapas, A. and Creatsas, G. and Michalas, S. and Antsaklis, A. and Koutsilieris, M.", journal = "Annals of the New York Academy of Sciences", year = "2006", volume = "1092", pages = "434-439", publisher = "Blackwell Publishing Inc.", issn = "0077-8923, 1749-6632", doi = "10.1196/annals.1365.042", keywords = "messenger RNA; somatomedin C; isoprotein; messenger RNA; primer DNA; somatomedin C, comparative study; conference paper; controlled study; correlation analysis; cyst; endometriosis; endometrium; endometrium tumor; female; fibrosis; gene expression; human; human tissue; laparoscopy; pathogenesis; protein expression; protein synthesis; article; case control study; cyst; endometriosis; endometrium; gene expression regulation; genetics; metabolism; polymerase chain reaction, Case-Control Studies; Cysts; DNA Primers; Endometriosis; Endometrium; Female; Gene Expression Regulation; Humans; Insulin-Like Growth Factor I; Polymerase Chain Reaction; Protein Isoforms; RNA, Messenger", abstract = "Pathogenesis of endometriosis involves growth factors, which are synthesized locally. Insulin-like growth factor-1 (IGF-1) prevents apoptosis and has mitogenic action on endometrial cells. The IGF-1 gene undergoes alternative splicing and results in three isoforms (IGF-1Ea, IGF-1Eb, and IGF-1Ec or MGF). We analyzed the mRNA expression of IGF-1 isoforms in tissue samples of eutopic endometrium and endometriotic cyst obtained during laparoscopy from women with endometriosis. We documented that all three IGF-1 isoforms are expressed in both eutopic endometrium and ovarian endometrioma. Furthermore,we documented a significant decrease in all IGF-1 isoform expression in endometriotic cyst compared to endometrium of women with endometriosis. The reduction may correlate with the disease status and presence of fibrotic inactive tissue found in late stages of the disease. © 2006 New York Academy of Sciences." }