Transcription Factors GATA-4 and GATA-6 and a GATA Family Cofactor, FOG-2, Are Expressed in Human Ovary and Sex Cord-Derived Ovarian Tumors*

Autor: Ilkka Ketola, Ralf Bützow, Olli Ritvos, Mika Laitinen, David B. Wilson, Mikko Anttonen, Markku Heikinheimo
Rok vydání: 2000
Předmět:
Endocrinology
Diabetes and Metabolism

Clinical Biochemistry
Biochemistry
0302 clinical medicine
Endocrinology
GATA6 Transcription Factor
RNA
Neoplasm

Cloning
Molecular

Cells
Cultured

In Situ Hybridization
Ovarian Neoplasms
0303 health sciences
Reverse Transcriptase Polymerase Chain Reaction
Theca Cell
Zinc Fingers
Middle Aged
Immunohistochemistry
3. Good health
DNA-Binding Proteins
Gene Expression Regulation
Neoplastic

Blotting
Southern

medicine.anatomical_structure
Theca
030220 oncology & carcinogenesis
embryonic structures
Female
Folliculogenesis
DNA Probes
Adult
endocrine system
medicine.medical_specialty
Ovary
In situ hybridization
Biology
03 medical and health sciences
Corpus Luteum
Internal medicine
medicine
Humans
Sex Cord-Gonadal Stromal Tumors
Ovarian follicle
Aged
030304 developmental biology
Granulosa Cells
urogenital system
Biochemistry (medical)
Antral follicle
GATA4 Transcription Factor
Cell culture
Transcription Factors
Zdroj: The Journal of Clinical Endocrinology & Metabolism. 85:3476-3483
ISSN: 1945-7197
0021-972X
Popis: Previous studies have implicated transcription factors GATA-4 and GATA-6 in the regulation of murine ovarian development and function. In rodents, GATA-4 is expressed in granulosa cells of primary and early antral follicles, whereas GATA-6 is expressed in granulosa cells of late antral follicles and luteal glands. Both transcription factors can be detected in lesser amounts in theca cells and interstitial cells. We have now examined the expression of GATA-4 and GATA-6 in human ovaries, human granulosa-luteal (GL) cells and sex cord-derived tumors. We show by in situ hybridization and immunohistochemistry that GATA-4 and GATA-6 messenger RNA (mRNA) and GATA-4 protein are present in granulosa and theca cells in both preantral and antral follicles. Both human ovarian tissue samples and freshly isolated GL cells derived from preovulatory follicles of gonadotropin-treated women express GATA-4, GATA-6, and FOG-2 transcripts, and GATA-6 mRNA expression in GL cell cultures is stimulated by human CG and 8-bromo-cAMP. The vast majority of granulosa and theca cell tumors examined expressed GATA-4 and GATA-6. We also found that mRNA for FOG-2, a recently discovered regulator of GATA-4, is coexpressed with GATA-4 in human ovary samples, normal granulosa cells, and in sex cord-derived tumors. Our results demonstrate that GATA-4, GATA-6, and FOG-2 are expressed in human ovary and in granulosa and theca cell tumors. Our findings support a role for GATA-binding proteins in human ovarian folliculogenesis. Moreover, these data suggest that GATA factors may contribute to the phenotypes of sex cord-derived ovarian tumors.
Databáze: OpenAIRE