2006 Fiscal Year Final Research Report Summary
Molecular pathology of the functional differentiation of the pituitary adenoma
Project/Area Number |
16390110
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Human pathology
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Research Institution | Tokai University |
Principal Investigator |
OSAMURA Yoshiyuki Tokai University, School of Medicine, Professor, 医学部, 教授 (10100992)
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Co-Investigator(Kenkyū-buntansha) |
UMEMURA Shinobu Tokai University, School of Medicine, Associate Professor, 医学部, 助教授 (20276794)
TAKEKOSHI Susumu Tokai University, School of Medicine, Associate Professor, 医学部, 助教授 (70216878)
KAJIWARA Hiroshi Tokai University, School of Medicine, Assistant Professor, 医学部, 講師 (20317754)
KIMURA Minoru Tokai University, School of Medicine, Professor, 医学部, 教授 (10146706)
TERAMOTO Akira Nippon Medical School, School of Medicine, Professor, 医学部, 教授 (60231445)
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Project Period (FY) |
2004 – 2006
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Keywords | Pituitary / αSU / FOXL2 / Adenoma |
Research Abstract |
[AIM] Many transcription factors play important roles in function and differentiation of the human pituitary adenomas. Forkhead box transcription factor L2, Fox12, is expressed during mouse pituitary development and co-localizes with expression of the glycoprotein hormone a subunit (aGSU). In addition, FOXL2 regulates expression of the aGSU gene in cell culture. To elucidate the functional role of FOXL2 in human pituitary, we detected the localization and expression of FOXL2 in normal human pituitaries and various types of its adenomas. [MATERIALS AND METHODS] The human pituitary adenomas were obtained by trans-sphenoidal surgery from 66 patients. Two normal adult pituitaries were obtained from the autopsies of non-endocrine cases. The localization of FOXL2 and pituitary hormones in these pituitary patients was studied by immunohistochemical staining. The quantitative analysis of FOXL2 protein was detected by using immunoblotting. [RESULTS AND DISCUSSION] FOXL2 was localized immunohistochemically in many of gonadotropin producing adenomas (Gn-omas), and in about 20% of normal pituitaries that also co-expressed aGSU. These results are consistent with the idea that FOXL2 plays a role in αGSU expression in human pituitary adenomas. Future studies with gain and loss of function animal models will be important to assess the function of FOXL2 in establishing and maintaining differentiated αGSU expressing cells.
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Research Products
(12 results)