Functions and Mechanisms of Tumor Necrosis Factor-α and Noncoding RNAs in Bone-Invasive Pituitary Adenomas
| Autor: | Hua Gao, Yazhou Miao, Haibo Zhu, Wei Dong, Jing Guo, Yutao Shen, Ya-Zhuo Zhang, Chuzhong Li |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Adenoma Adult Male Cancer Research RNA Untranslated Adolescent Biology 03 medical and health sciences Young Adult Pituitary adenoma Osteoclast microRNA medicine Humans Gene Regulatory Networks Neoplasm Invasiveness Pituitary Neoplasms Aged Neoplasm Staging Regulation of gene expression Tumor Necrosis Factor-alpha Gene Expression Profiling Cancer Reproducibility of Results Middle Aged medicine.disease Prognosis Magnetic Resonance Imaging Gene expression profiling Gene Expression Regulation Neoplastic 030104 developmental biology medicine.anatomical_structure Oncology Cancer research Immunohistochemistry Tumor necrosis factor alpha Female Transcriptome |
| Zdroj: | Clinical cancer research : an official journal of the American Association for Cancer Research. 24(22) |
| ISSN: | 1557-3265 |
| Popis: | Purpose: To explore the molecular mechanism and prognosis of bone-invasive pituitary adenomas (BIPA). Experimental design: A total of 274 patients with pituitary adenomas were followed up. Transcriptomic microarrays analysis was performed on 10 pituitary adenomas, including five BIPAs and five non-bone-invasive pituitary adenomas (NBIPA). The targeted molecular markers were validated by qRT-PCR, IHC, ELISA, and osteoclast differentiation. Results: Clinical variable analyses revealed a significant correlation between bone invasion and female sex, large tumor volume, non-gross total resection (NGTR), and tumor regrowth. BIPAs had worse progression-free survival (PFS) than did NBIPAs in the NGTR and nonfunctional pituitary adenoma (NFPA) groups. Gene ontology functional and KEGG pathway analyses showed that the biological processes and pathways were primarily immune and inflammatory pathways. Pathway act work showed that osteoclast differentiation pathway was significantly implicated in the pathway network. BIPAs had higher expression of TNFα than that of NBIPAs on IHC. In vitro, TNFα could induce RAW264.7 cells to differentiate into mature osteoclasts, leading to bone destruction. NR_033258, lncRNA SNHG24, miR-181c-5p, and miR-454-3p can regulate TNFα expression. Conclusions: BIPAs had worse PFS than did NBIPAs in the NGTR and NFPA groups. Inflammatory and immune factors play an important role in BIPAs. TNFα can directly induce osteoclast differentiation in BIPAs. NR_033258, lncRNA SNHG24, miR-181c-5p, and miR-454-3p can regulate TNFα expression. TNFα and its related lncRNAs and miRNAs represent potential therapeutic targets for bone-invasive pituitary adenomas in the future. Clin Cancer Res; 24(22); 5757–66. ©2018 AACR. |
| Databáze: | OpenAIRE |
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