Adult ovarian granulosa cell tumor transcriptomics: prevalence of FOXL2 target genes misregulation gives insights into the pathogenic mechanism of the p.Cys134Trp somatic mutation

• Published in: Oncogene Vol. 32; no. 22; pp. 2739 - 2746
• Main Authors: Benayoun, B A, Anttonen, M, L’Hôte, D, Bailly-Bechet, M, Andersson, N, Heikinheimo, M, Veitia, R A
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 30.05.2013; Nature Publishing Group; Nature Publishing Group [1987-....]
• Subjects: 631/208/212/2019; 692/420/2489/144/68; 692/699/67/1517/1709; Adult; Aged; Apoptosis; Biochemistry, Molecular Biology; Cancer; Cell Biology; Cell cycle; Cell death; Cell Line, Tumor; Cell Proliferation; Development and progression; Female; Forkhead Box Protein L2; Forkhead Transcription Factors - genetics; Gene Expression Profiling; Gene mutations; Genetic aspects; Genetic transformation; Granulosa Cell Tumor - genetics; Granulosa Cells - metabolism; Granulosa Cells - pathology; Health aspects; HeLa Cells; Human Genetics; Humans; Internal Medicine; Life Sciences; Medicine; Medicine & Public Health; Middle Aged; Mutation; Oncology; original-article; Ovarian cancer; Ovarian Neoplasms - genetics; Ovaries; Ovary - pathology; Pathogenesis; Prevalence studies (Epidemiology); Risk factors; Transcriptome - genetics; Transcriptomics; Tumors; Finland; ovary; FOXL2; ovarian granulosa cell tumor; transcriptome
• ISSN: 0950-9232; 1476-5594
• DOI: 10.1038/onc.2012.298

Ovarian granulosa cell tumors (OGCT) are the most frequent kind of sex cord-stromal tumors, and represent ∼2–5% of all ovarian malignancies. OGCTs exist as two entities, juvenile and adult types, with specific clinical and pathological characteristics. The molecular pathogenesis of these tumors has just begun to be unraveled. Indeed, recent studies have indicated that mutation and/or misregulation of the key ovarian transcription factor FOXL2 has a role in OGCT formation, although the mechanisms remain unclear. To better understand the molecular characteristics of OGCT, we studied the transcriptomic profiles of ten human adult-type OGCT samples, as well as ethnically matched granulosa cell (GC) controls. We find that the OGCT samples analyzed herein exhibit several hallmarks of cancer, including increased expression of genes linked to cell proliferation, but decreased expression of those conferring sensitivity to cell death. Moreover, genes differentially expressed in OGCTs are significantly enriched for known FOXL2 target genes, consistently with the prevalence of FOXL2 somatic mutation in these tumors. Expression of these targets is altered in a way expected to promote malignant transformation, for instance, through induction of genes associated with faster cell cycling and downregulation of genes associated with cell death. Over time, such defects may be responsible at least partly for the malignant transformation of healthy GCs into OGCT. These insights into the molecular pathogenesis of OGCTs may open the way to new efforts in the development of more targeted therapeutic strategies for OGCT patients.