Gold nanocages (AuNCs) are comparatively novel nanostructures, as many of their characteristics are still to be exploited. The purpose of present study was to systematically investigate the toxicological effects of AuNCs on human keratinocyte cell line (HaCaT) utilizing Dark Field (DF)/Bright Field (BF) imaging and flow cytometry cell cycle techniques. We have applied surface modification, concentration, and incubation time of AuNCs as variables to investigate their effect on the cellular imaging and cell cycle response of HaCaT cells. The results indicate that the AuNCs interact with HaCaT cells in accordance to their surface charge and concentration. Cellular uptake is evident from DF images which lead to the cell cycle perturbations and apoptosis in HaCaT cells. AuNCs cause a prominent G2/M phase arrest after 24 h of incubation. To the best of our knowledge toxicological effects of AuNCs on cell cycle of HaCaT cell line in vitro are not reported previously.
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http://dx.doi.org/10.1016/j.fct.2016.08.014 | DOI Listing |
Cell Biol Toxicol
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Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, No. 36 Sanhao Street, Heping District, Shenyang , Liaoning Province, China.
NFKB1, a core transcription factor critical in various biological process (BP), is increasingly studied for its role in tumors. This research combines literature reviews, meta-analyses, and bioinformatics to systematically explore NFKB1's involvement in tumor initiation and progression. A unique focus is placed on the NFKB1-94 ATTG promoter polymorphism, highlighting its association with cancer risk across diverse genetic models and ethnic groups, alongside comprehensive analysis of pan-cancer expression patterns and drug sensitivity.
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View Article and Find Full Text PDFNucleosides Nucleotides Nucleic Acids
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Division of Hematology, Department of Internal Medicine, Medical Faculty, Tekirdağ Namık Kemal University, Tekirdağ, Turkey.
Breast cancer is the most common malignancy that affects women. MicroRNAs (miRNAs) play an essential role in cancer therapy and regulate many biological processes such as cisplatin resistance. The study's objective was to determine whether miR-182 dysregulation was the cause of cisplatin resistance in TNBC cell line MDA-MB-231.
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MOE Key Laboratory of Biosystems Homeostasis and Protection, College of Life Sciences, Zhejiang University, No.866 Yuhangtang Road, 310058, Hangzhou, China.
Meiosis in mammalian oocytes is interrupted by a prolonged arrest at the germinal vesicle stage, during which oocytes have to repair DNA lesions to ensure genome integrity or otherwise undergo apoptosis. The FIRRM/FLIP-FIGNL1 complex dissociates RAD51 from the joint DNA molecules in both homologous recombination (HR) and DNA replication. However, as a type of non-meiotic, non-replicative cells, whether this RAD51-dismantling mechanism regulates genome integrity in oocytes remains elusive.
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January 2025
Department of Pathology and Genomic Medicine, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
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