Onosma mutabilis-mediated silver nanoparticles target lung cancer cell viability and migration: in vitro evidence from A549 model Pelin Eroglu, Selda Doğan Çalhan, Hamide Doğan Drug Development and Industrial Pharmacy, 2026 ObjectiveSilver nanoparticles (AgNPs) are widely utilized in anti-migratory applications due to their beneficial physicochemical and biological properties. This study aimed to evaluate the in vitro cytotoxic and anti-migratory effects of AgNPs synthesized using the above-ground parts (stems, flowers, and leaves) of Onosma mutabilis (O. mutabilis).SignificanceGreen-synthesized AgNPs derived from O. mutabilis exhibit notable cytotoxic and anti-migratory effects on A549 cells, offering dual-functional potential. Their biocompatibility and capacity for targeted release in acidic tumor microenvironments make them promising candidates for sustainable cancer therapies.MethodsAgNPs were green-synthesized using aqueous plant extracts and characterized by ultraviolet-visible spectroscopy (UV-Vis spectroscopy), X-ray diffraction (XRD), fourier transform infrared (FTIR), and scanning electron microscopy (SEM). Cytotoxicity against A549 cells was assessed via the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay and anti-migratory effects were examined using a scratch assay.ResultsUV–Vis spectroscopy confirmed the formation of AgNPs synthesised from O. mutabilis extracts by showing a characteristic absorption band around 420–480 nm. XRD analysis revealed their crystalline structure, while SEM demonstrated predominantly spherical morphology. MTT assay indicated that the AgNPs, especially those derived from the flower extract, significantly reduced A549 cell viability in a dose- and time-dependent manner, with an IC50 value of 5.28 µg/mL. In addition, wound healing assays confirmed their strong anti-migratory activity.ConclusionThese findings suggest that green-synthesised AgNPs induce cytotoxic and anti-migratory effects, highlighting their potential as therapeutic agents against A549 lung cancer cells.
Extraction-Dependent Immunomodulatory and Angiogenesis-Related Molecular Responses of Nigella sativa Oil in Adipose-Derived Mesenchymal Stem Cells Badel Ince, Gokturk Avsar, Cagatay Han Turkseven, Pelin Eroglu, Gamze Ayar, Murat Eser Akyurek Folia Biologica Czech Republic, 2026 Nigella sativa black cumin oil (BCO) exhibits well-documented anti-inflammatory and antioxidant properties; however, the impact of extraction-related compositional variation on its cellular and molecular effects in stem cell systems remains insufficiently characterized. This study investigated the effects of cold-pressed (CP) and supercritical CO 2 (ScCO 2 )-extracted BCO on the viability, inflammatory response and angiogenic potential of adipose-derived mesenchymal stem cells (ASCs). The oil composition and antioxidant activity were assessed using GC/MS and DPPH assays, respectively. ASCs were treated with different volumes of BCO, and cell viability was evaluated at 24, 48 and 72 h using the MTT assay. Anti-inflammatory effects were evaluated by real-time PCR analysis of IL6 and IL10 mRNA expression, while angiogenesis-related molecular responses were evaluated based on VEGF mRNA expression. Both CP and ScCO 2 -extracted BCO significantly increased ASC viability in a volume-dependent manner, with the highest viability consistently observed at 100 µl (P < 0.05). Treatment with 50 µl and 100 µl of either oil significantly reduced IL6 expression and concomitantly increased IL10 expression at 24 and 48 h (P < 0.05). VEGF expression was also significantly up-regulated at these time points, with ScCO 2 -extracted BCO inducing a more pronounced and sustained angiogenic response (P < 0.05). These findings indicate that BCO enhances ASC viability and molecular responses in a volume-dependent manner, while differences associated with extraction-related compositional variation may modulate inflammation- and angiogenesis-related molecular signalling in ASCs.
Evaluation of phytochemical profiling, antioxidant and antimicrobial activities of Cionura erecta latex: the first report of the therapeutic potential of a natural exudate Selda Dogan Calhan, Pelin Eroglu, Zehra Oksuz, Ece Cobanoglu, Ozlem Nekuk, Mustafa Gundogan, Nefise Ozlen Sahin Natural Product Research, 2026 This study provides the first detailed evaluation of C. erecta latex, an uncharacterised exudate of the Apocynaceae family, focusing on its phytochemical composition and bioactivity. HPLC analysis revealed nine phenolic compounds, mainly sinapic acid (4876.2 µg/g), ferulic acid (902.6 µg/g), and epicatechin (386.5 µg/g). Although the total phenolic content was relatively low (2.27 ± 4.2 mg GAE/g), DPPH assay indicated moderate antioxidant activity (IC50 = 114 µg/mL), suggesting contributions from other bioactive constituents. Volatile profiling via HS-SPME-GC-MS and solvent-assisted GC–MS identified compounds such as p-cymene (14.05%), 2-hexanol (12.52%), and kaur-16-ene (72.06%). The latex exhibited antimicrobial activity against bacteria and yeasts, with MIC values ranging from 62.5 to 250 µg/mL, showing higher effectiveness against Acinetobacter baumannii, Candida parapsilosis, and Candida glabrata. Overall, the findings highlight C. erecta latex as a phenol- and terpenoid-rich natural product with promising antioxidant and antimicrobial potential, supporting its traditional dermatological use and future pharmaceutical relevance.
Hemp Seed Oils in Stem Cell Therapy: Cold Pressed vs. Supercritical CO2 Extraction? Badel Ince, Gokturk Avsar, Cagatay Han Turkseven, Pelin Eroglu, Gamze Ayar, Murat Eser Akyurek Bratislava Medical Journal, 2025 Objective This study aims to evaluate the effects of hemp seed oil (HSO) on adipose-derived stem cells (ASCs) to enhance tissue repair, regulate inflammation, and promote angiogenesis. Background HSO, rich in bioactive compounds, was obtained via cold press (CP) and supercritical carbon dioxide (ScCO2) methods to assess its effects on cytokines and vascular endothelial growth factor (VEGF) in ASCs. Methods Chemical composition were assessed via gas chromatography-mass spectrometry (GC–MS) and antioxidant activity was determined by measuring the % radical scavenging activity (RSA) with 1,1-diphenyl-2-picrylhydrazyl (DPPH). ASCs were treated with HSO and, cell viability was measured at 24, 48, and 72 h using the methyl thiazolyl tetrazolium (MTT). Gene expression of interleukin-6 (IL-6), interleukin-10 (IL-10), and VEGF was quantified by real-time PCR. Results The CP-fixed HSO had higher linoleic (48.48%) and oleic acid (29.33%) content than ScCO2-extracted HSO. Phenolic content and antioxidant activity were greater in CP-fixed HSO [57.85 mgGAE (mgGallic Acid Equivalent)/g, 68.8%] than in ScCO2-extracted HSO (58.5 mgGAE/g, 19.9%). Cell viability increased significantly with 75 and 100 µL of CP-fixed HSO at 48 and 72 h (p < 0.05). CP-fixed HSO up-regulated IL-10 and reduced IL-6 at 24 and 48 h (p < 0.05), while also increasing VEGF with 50 and 100 µL at 24 and 48 h (p < 0.05). ScCO2-extracted HSO primarily up-regulated IL-10 but had limited effects on IL-6 and VEGF. Conclusions CP-fixed HSO had superior phenolic content, antioxidant activity, and enhanced ASC viability, anti-inflammatory effects, and angiogenesis, suggesting strong therapeutic potential for stem cell use.
Comparison of classical and flowcytometric osmotic fragility and flowcytometric eosin-5-maleimide binding tests in diagnosis of hereditary spherocytosis Cemil Gülüm, Pelin Eroğlu, Gülhan Temel, Anıl Tombak, Selma Ünal Turkish Journal of Biochemistry, 2025 Objectives Hereditary spherocytosis (HS) is the most common congenital hemolytic anemia in Northern Europe and North America. Damaged or deficient proteins in the erythrocyte membrane cause the condition, leading to a decrease in the surface area and volume of erythrocytes. Specialists traditionally use the osmotic fragility test (C-OF) for diagnosis. Researchers have developed new methods for flow cytometry-based tests that are the eosin-5-maleimide binding (EMA) and osmotic fragility (FC-OF) tests. In this study, we aimed to determine and compare the power of discrimination of FC-OF, EMA, and C-OF tests. Another purpose is to investigate the effect of incubation. Methods We performed both real-time and incubated C-OF, EMA, and FC-OF on 20 patients diagnosed with HS and 30 healthy controls. We diagnosed HS based on family history, spherocytes, and clinical and lab findings. Results We found that the success of all tests in the classification was statistically significant (p<0.001). The discriminatory power of C-OF was not different from that of EMA and FC-OF. FC-OF discriminated better than EMA. Incubation increased C-OF performance and decreased EMA and FC-OF performance. Conclusions We think FC-OF should be preferred. Because it has higher discrimination power, specificity, and sensitivity. It gives faster results, costs less, and needs less labor. The lack of flow cytometer devices in every center is the biggest handicap of FC-OF and EMA. But we think that the FC-OF method can be adapted to hemogram devices available in every center in the future.
Investigation of biological activities of silver nanoparticles synthesis from the root extract of endemic Onosma mutabilis (O. mutabilis) Plant Pelin Eroğlu, Fidan Valiyeva Spectroscopy Letters, 2025 Plant-mediated silver nanoparticles (AgNPs) synthesis appears to be reliable and environmentally friendly, requiring less energy, and cost. Various components present in its natural products can function as strong reducing and capping substrates, ensuring the stability of the resulting NPs. This study synthesized AgNPs with root extracts of O. mutabilis. The effect of many different synthesis parameters (such as silver ion concentration, temperature and reaction pH) of the obtained root extract on the synthesis of AgNPs was also examined. Furthermore, AgNPs were characterized using UV-Vis spectroscopy, Fourier-transformed infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), particle size measurement (Malvern Mastersizer) and energy dispersive X-ray analysis (EDX). The surface plasmon resonance band features of AgNPs were determined in the ultraviolet-visible absorbance spectrum at 410 nm. Total phenolic compound (TPC) determination was analyzed using the Folin-Ciocalteu method, and TPC in AgNPs extracts was determined as 295 ± 0.02 mg GAEs/gr extract. The antioxidant activity of the AgNPs was examined using the 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) free radical scavenging activity method. The synthesized AgNPs exhibited strong antioxidant activity. The antidiabetic activity was determined by measuring alpha-amylase inhibition by spectrophotometric method. α-amylase inhibition values were determined to be highest at 31%. The study was further elaborated for determining AgNPs antibacterial using MIC. The biosynthesized AgNPs showed effective antibacterial activity against the Acinetobacter baumannii (A.baumannii) bacteria.Suggests that green biosynthesized AgNPs can constitute an effective antioxidant, antidiabetic and antibacterial agent.
Assessment and comparison of phytochemical constituents and biological activities of endemic Odonterrhena floribunda (Brassicaceae) from Türkiye Yasemin Salık, Pelin Eroglu, Gökhan Zengin, Rıza Binzet International Journal of Environmental Health Research, 2025 This study aimed to evaluate the phenolic profile, antioxidant, antibacterial, and antidiabetic properties of ethanolic and methanolic extracts of the different parts of the endemic Odontarrhena floribunda. The antioxidant activities of O. floribunda were determined with 1,1-diphenyl-1-picrylhydrazyl (DPPH) and the copper-reducing antioxidant capacity (CUPRAC) assays. The strongest antioxidant activity was recorded in methanolic root extract (IC50:1.68±0.25 μg/mL) for DPPH and ethanolic root (λ450:0.68±0.20) extract for CUPRAC. Antibacterial activities of the extracts were displayed by the Resazurin Microplate Method (REMA). All plant extracts analyzed demonstrated stronger effects on Acinetobacter baumannii (ATCC 02026) than those of the standard compound. The in vitro α-amylase and α-glucosidase inhibitory of the plant extract were assessed using the Iodine method. Except for the methanol leaf extract, all other extracts showed strong α-glucosidase inhibitory activity (0.88-2.13 mmolTE/g). These results show that this endemic O. floribunda is a potential natural antioxidant, antibacterial, and enzyme inhibitor source.
The relationship between the urokinase-type plasminogen activator gene Pro141Leu polymorphism and patients with prostate cancer Cemil Gülüm, Pelin Eroğlu, Rojda Tanrıverdi, Murat Bozlu Revista Da Associacao Medica Brasileira, 2025 SUMMARY OBJECTIVE: Although many genes associated with prostate cancer have been identified, there are still many cases of prostate cancer whose genetics have not been identified. The urokinase-type plasminogen activator gene is thought to play a key role in cancer invasion and metastasis. The Pro141Leu polymorphism may be involved in the development of prostate cancer, although genetic evidence is lacking. METHODS: We used the real time polymerase chain reaction based TaqMan assay to investigate whether the urokinase-type plasminogen activator gene Pro141Leu polymorphism is associated with prostate cancer patients and healthy controls. urokinase-type plasminogen activator, urokinase-type plasminogen activator receptor, and prostate-specific antigen antigens were assayed by the enzyme-linked immunosorbent assay method. RESULTS: We found no significant differences between the cancer and control populations in terms of genotype distribution (CC, CT, and TT). Furthermore, we found no association between the urokinase-type plasminogen activator gene Pro141Leu polymorphism and cancer risk in prostate cancer patients. CONCLUSION: This is the first study to investigate the association between the rs2227564 polymorphism and prostate cancer. Although the urokinase-type plasminogen activator gene Pro141Leu polymorphism has been reported to be a risk factor for some cancers, our findings suggest that the urokinase-type plasminogen activator gene Pro141Leu polymorphism is not an important genetic risk factor for prostate cancer.
Investigation of the Effect of Tamoxifen on hERG1 Potassium Channel Gene Expression in MCF-7 Cell Line P. Eroglu, F. Sogut, D. Yetkin, S. Yalin, U. Comelekoglu, S. N. Yilmaz, S. Erdoğan Russian Journal of Bioorganic Chemistry, 2024 Abstract Objective: Tamoxifen (TAM) is a nonstreroidal antiestrogenic pharmaceutical agent extensively employed in the therapeutic management of breast cancer. Alterations in the expression patterns of diverse ion channels have been implicated in the pathophysiology of breast cancer. The principal objective of this investigation was to elucidate the impact of TAM on the expression of the hERG1 potassium channel in the MCF-7 cell line. Methods: Cytotoxicity induced by TAM across various concentrations was assessed through the utilization of the MTT method. The patch clamp method was employed for electrophysiological analyses. The gene expression of the hERG1 potassium channel was quantified utilizing RT-qPCR. Results: The electrophysiological findings revealed reduction in potassium channel currents, reaching maximal inhibition at a TAM concentration of 5 μM. Concurrently, hERG1 potassium channel gene expression exhibited a decrease at the 5 μM TAM concentration. Despite statistical analysis, no statistically significant values were identified in both potassium channel currents and gene expression analyses when compared to the control group. Our results demonstrate that the blocking effect of TAM on potassium channel currents in the MCF-7 cell line was not determined. Conclusions: Further investigations are warranted to elucidate comprehensively the role of TAM in modulating hERG1 in breast cancer.
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Oxidative stress and antioxidant enzyme activities in patients with cutaneous leishmaniasis in endemic region of Hatay (ANTIOCH) Asian Journal of Chemistry, 2007
Cadmium induced changes in lipid peroxidation and antioxidant status in brain of ovariectomized rats Asian Journal of Chemistry, 2006
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