# Oxidative Phosphorylation in Silent Pituitary Adenomas: A Multiomics Perspective

**Authors:** Yuan Chen, Qiang Zhao, Xing Wang, Xinling Wang, Yanying Guo

PMC · DOI: 10.1155/ije/8488950 · International Journal of Endocrinology · 2026-01-28

## TL;DR

This study explores how oxidative phosphorylation affects hormone secretion in silent pituitary adenomas using multiomics data and cell line experiments.

## Contribution

The study identifies oxidative phosphorylation as a key pathway in silent pituitary adenomas and validates its role in hormone secretion and tumor behavior.

## Key findings

- Oxidative phosphorylation pathway is enriched in silent pituitary adenomas.
- Electron transfer chain inhibitors restore hormone secretion in pituitary adenoma cell lines.
- MAPK1 and PKM knockdown reduces hormone secretion and apoptosis in cell lines.

## Abstract

Although the World Health Organization has clearly defined silent pituitary adenomas (SPAs) and functional adenomas (non‐SPAs), the detailed biological mechanisms remain unclear. This study conducted a comprehensive analysis of clinical, genomic, transcriptomic, and proteomic differences between SPA and non‐SPA. The results revealed significant differences in mutational profiles, with a notably higher mutation rate of the TCHH gene in non‐SPA samples. Transcriptomic and proteomic analyses identified distinct expression patterns, highlighting the enrichment of the oxidative phosphorylation pathway and other related Gene Ontology terms in SPA samples. To validate these findings, 11 additional pituitary adenoma samples were analyzed, confirming the critical role of oxidative phosphorylation in SPA. Activation of oxidative phosphorylation altered the hormone secretion, and the electron transfer chain inhibitor restored this in both human and rat pituitary adenoma cell lines. Furthermore, a protein–protein interaction network was constructed, revealing key regulatory differences between SPA and non‐SPA, and identifying MAPK1, MAPK3, IDH1, and PKM as key hubs in the network. MAPK1 and PKM knockdown significantly reduced the hormone secretion and apoptosis of both cell lines. These findings suggest that the oxidative phosphorylation pathway plays a pivotal role in the secretory functions of pituitary adenomas. This study offers new insights into the biological mechanisms underlying pituitary adenomas and provides valuable directions for future research, emphasizing the importance of oxidative phosphorylation in tumor behavior and potential therapeutic targets.

## Linked entities

- **Genes:** TCHH (trichohyalin) [NCBI Gene 7062], MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594], MAPK3 (mitogen-activated protein kinase 3) [NCBI Gene 5595], IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417], PKM (pyruvate kinase M1/2) [NCBI Gene 5315]
- **Diseases:** pituitary adenoma (MONDO:0006373)

## Full-text entities

- **Genes:** PKM (pyruvate kinase M1/2) [NCBI Gene 5315] {aka CTHBP, HEL-S-30, OIP3, PK3, PKM2, TCB}, IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}, MAPK3 (mitogen-activated protein kinase 3) [NCBI Gene 5595] {aka ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1}, SFTPA1 (surfactant protein A1) [NCBI Gene 653509] {aka COLEC4, ILD1, PSP-A, PSPA, SFTP1, SFTPA1B}, TCHH (trichohyalin) [NCBI Gene 7062] {aka THH, THL, TRHY, UHS3}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}
- **Diseases:** adenomas (MESH:D000236), tumor (MESH:D009369), Pituitary Adenomas (MESH:D010911)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

32 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12849212/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12849212/full.md

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Source: https://tomesphere.com/paper/PMC12849212