DNA Damage Response Induced by Etoposide Promotes Steroidogenesis Via GADD45A in Cultured Adrenal Cells
Authors
Affiliations
Glucocorticoid production is regulated by adrenocorticotropic hormone (ACTH) via the cyclic adenosine monophosphate (cAMP)/protein kinase A (PKA) pathway in the adrenal cortex, but the changes in steroidogenesis associated with aging are unknown. In this study, we show that cell-autonomous steroidogenesis is induced by non-ACTH- mediated genotoxic stress in human adrenocortical H295R cells. Low-dose etoposide (EP) was used to induce DNA damage as a genotoxic stress, leading to cellular senescence. We found that steroidogenesis was promoted in cells stained with γH2AX, a marker of DNA damaged cells. Among stress-associated and p53-inducible genes, the expression of GADD45A and steroidogenesis-related genes was significantly upregulated. Immunofluorescence analysis revealed that GADD45A accumulated in the nuclei. Metabolite assay using cultured media showed that EP-treated cells were induced to produce and secrete considerable amounts of glucocorticoid. Knockdown of GADD45A using small interfering RNA markedly inhibited the EP-induced upregulation of steroidogenesis-related gene expression, and glucocorticoid production. A p38MAPK inhibitor, but not a PKA inhibitor, suppressed EP-stimulated steroidogenesis. These results suggest that DNA damage itself promotes steroidogenesis via one or more unprecedented non-ACTH-mediated pathway. Specifically, GADD45A plays a crucial role in the steroidogenic processes triggered by EP-stimulated genotoxic stress. Our study sheds new light on an alternate mechanism of steroidogenesis in the adrenal cortex.
Locking the gates of immortality: targeting alternative lengthening of telomeres (ALT) pathways.
Mishra A, Patel T Med Oncol. 2025; 42(3):78.
PMID: 39964637 DOI: 10.1007/s12032-025-02627-2.
Increased DNA damage in full-grown oocytes is correlated with diminished autophagy activation.
Sun F, Ali N, Londono-Vasquez D, Simintiras C, Qiao H, Ortega M Nat Commun. 2024; 15(1):9463.
PMID: 39487138 PMC: 11530536. DOI: 10.1038/s41467-024-53559-w.
Okudaira N, Akimoto M, Susa T, Akimoto M, Hisaki H, Iizuka M Aging Cell. 2024; 23(9):e14206.
PMID: 38769821 PMC: 11488315. DOI: 10.1111/acel.14206.
Tang M, Yin S, Zeng H, Huang A, Huang Y, Hu Z Cell Death Dis. 2024; 15(1):69.
PMID: 38238314 PMC: 10796917. DOI: 10.1038/s41419-023-06418-3.
Salvato I, Ricciardi L, Dal Col J, Nigro A, Giurato G, Memoli D Front Immunol. 2023; 14:1192028.
PMID: 37483631 PMC: 10360199. DOI: 10.3389/fimmu.2023.1192028.