Evaluation of the Effects of Asprosin on Cell Viability and DNA Damage on Human Glioblastoma and Mouse Neuroblastoma Cell Lines

Asprosin is a peptide hormone secreted from white adipose tissue during fasting and plays a role in the regulation of energy metabolism. Its ability to cross the blood–brain barrier and exert effects on the central nervous system has attracted attention regarding neurological disorders and brain tumors. Recent studies suggest that asprosin may also be involved in tumor biology. This study investigated the effects of asprosin on cell viability and DNA damage in human glioblastoma (U87-MG) and mouse neuroblastoma (N2a) cell lines. Cells were treated with 1, 10, and 100 ng/mL asprosin. Cell viability was assessed using the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay, while DNA damage was evaluated by the Comet assay. Data were analyzed using GraphPad Prism 9. One-way analysis of variance (ANOVA) followed by Tukey's post hoc test was used for statistical analysis, and p

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Journal
New Trends in Medicine Sciences
Published
2026-10-29
DOI
https://doi.org/10.56766/ntms.2013146
Primary Topic
Glioma Diagnosis and Treatment
Type
article
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Evaluation of the Effects of Asprosin on Cell Viability and DNA Damage on Human Glioblastoma and Mouse Neuroblastoma Cell Lines

Tuba Keskin, Samet Öz, Suat Tekin, Güldeniz Şekerci et al.
1 links
New Trends in Medicine Sciences
Glioma Diagnosis and Treatment
article

Evaluation of the Effects of Asprosin on Cell Viability and DNA Damage on Human Glioblastoma and Mouse Neuroblastoma Cell Lines

Tuba Keskin, Samet Öz, Suat Tekin, Güldeniz Şekerci, Zeynep Ergüneş
article en

Abstract

Asprosin is a peptide hormone secreted from white adipose tissue during fasting and plays a role in the regulation of energy metabolism. Its ability to cross the blood–brain barrier and exert effects on the central nervous system has attracted attention regarding neurological disorders and brain tumors. Recent studies suggest that asprosin may also be involved in tumor biology. This study investigated the effects of asprosin on cell viability and DNA damage in human glioblastoma (U87-MG) and mouse neuroblastoma (N2a) cell lines. Cells were treated with 1, 10, and 100 ng/mL asprosin. Cell viability was assessed using the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay, while DNA damage was evaluated by the Comet assay. Data were analyzed using GraphPad Prism 9. One-way analysis of variance (ANOVA) followed by Tukey's post hoc test was used for statistical analysis, and p

New Trends in Medicine SciencesVol. 7(3)
Osmaniye Korkut Ata University (TR), Inonu University (TR)
Good health and well-being
Openalex Percentile: Top 12%
Glioma Diagnosis and Treatment
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