scholarly journals Inhibin-Activin Receptor Subunit Gene Expression in Ovarian Tumors

2002 ◽  
Vol 87 (3) ◽  
pp. 1395-1401 ◽  
Author(s):  
Peter J. Fuller ◽  
Emma T. Zumpe ◽  
Simon Chu ◽  
Pam Mamers ◽  
Henry G. Burger
1995 ◽  
Vol 5 (6) ◽  
pp. 550-560 ◽  
Author(s):  
Schahram Akbarian ◽  
Molly M. Huntsman ◽  
James J. Kim ◽  
Alireza Tafazzoli ◽  
Steven G. Potkin ◽  
...  

2021 ◽  
Author(s):  
Tsukasa Kochiyama ◽  
Izumi Kawagoe ◽  
Ai Yamaguchi ◽  
Masataka Fukuda ◽  
Masakazu Hayashida

Abstract Background: Gamma-aminobutyric acid type A (GABAA) receptors are thought to play a role in the functioning of the immune system. GABAA receptors have 19 types of subunits, the components of which determine their physiological functions. However, the subunits that are expressed in immune cells during inflammation have not been fully investigated. Recent reports have shown that anesthetic agents may affect the gene expression of GABAA receptors subunits in immune cells. Therefore, we aimed to investigate the changes in GABAA receptor subunit gene expression during macrophage differentiation and propofol administration in order to clarify the relationship between the expression of GABAA receptors and the immunomodulatory effect of propofol.Methods: Human acute monocytic leukemia (THP-1) cells were differentiated into macrophage-like cells (M0 THP-1); subsequently, M0 THP-1 cells were differentiated into inflammatory M1 macrophage-like cells (M1 THP-1). Propofol was administered during the differentiation into M1 THP-1 cells. Using reverse transcriptase polymerase chain reaction, we examined which GABAA receptor subunit genes were expressed and whether there were changes in the gene expression during macrophage differentiation and propofol administration in THP-1 cells.Results: The expression of the α1, α4, β1, β2, γ1, and γ2 subunits increased during differentiation into M0 THP-1 cells. The expression of the α1, α4, β1, β2, γ2, and δ subunits decreased and that of the γ1 subunit increased during differentiation into M1 THP-1 cells. The gene expression of the α1, α4, and β2 subunits increased upon administering propofol during differentiation into M1 THP-1 cells.Conclusions: The gene expression of GABAA receptor subunits changed during macrophage differentiation in THP-1 cells. The expressions of α1 and α4 increased following propofol administration during the differentiation into M1 THP-1 cells, which may indicate that the GABAA receptor is involved in the immunosuppressive effects of propofol. This study can help in the choice of anesthetic agents for proinflammatory conditions such as highly-invasive surgery.


1993 ◽  
Vol 16 (12) ◽  
pp. 1332-1337 ◽  
Author(s):  
Henry J. Kaminski ◽  
Robert A. Fenstermaker ◽  
Fadi W. Abdul-Karim ◽  
Julie Clayman ◽  
Robert L. Ruff

2021 ◽  
Vol 81 (1) ◽  
pp. 43-57
Author(s):  
Mona Faraz ◽  
Nastaran Kosarmadar ◽  
Mahmoud Rezaei ◽  
Meysam Zare ◽  
Mohammad Javan ◽  
...  

2004 ◽  
Vol 22 (20) ◽  
pp. 4127-4134 ◽  
Author(s):  
Stephen S. Roberts ◽  
Motomi Mori ◽  
Patrick Pattee ◽  
Jodi Lapidus ◽  
Ravi Mathews ◽  
...  

Purpose Neuroblastoma (NB) is a common childhood malignancy characterized by heterogeneous clinical behavior. The purpose of this study was to identify potential NB biomarkers that may improve outcome prediction. Patients and Methods The suppression subtractive hybridization (SSH) technique was used to identify the genes differentially expressed between NB and control tissue. RNA isolated from 235 primary NB tumor samples obtained from the Children's Cancer Group was evaluated for expression of the candidate markers using quantitative reverse transcriptase polymerase chain reaction (Taqman assays). The association between the mRNA expression levels in the identified candidate genes and clinical outcome was evaluated. Results SSH analysis identified differential expression of members of the GABAergic gene family in NB. Lower levels of gamma-aminobutyric acid (GABA) receptor–associated protein (GABARAP) gene expression predict decreased survival among all patients. GABAA δ receptor subunit gene expression was predictive of a poor outcome among Evans stage IV-S patients. An index of five coexpressed GABAA receptor subunits was identified (GABAA profile [GAP score]). Patients with a higher GAP score (> −1) had a survival advantage. Multivariate analysis showed that GABARAP and GABAA α2 receptor subunit gene expression levels and GAP score remained predictors of clinical outcome after accounting for current prognostic indicators. Conclusion Dysregulation of the GABAergic system may constitute a fundamental event in the development of NB, and assessment of GABAergic system gene expression could provide improved patient stratification and potential new therapies.


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