Paracetamol Induces Apoptosis, Reduces Colony Formation, and Increases PTPRO Gene Expression in Human Embryonic Kidney HEK 293 Cells
    
Yazarlar (4)
Dr. Öğr. Üyesi Ayşe Nur COŞKUN DEMİRKALP Kırşehir Ahi Evran Üniversitesi, Türkiye
Akın Tekcan
Amasya University, Türkiye
Mustafa Çakır
Erciyes University, Türkiye
Hamiyet Altuntaş
Erciyes Üniversitesi, Türkiye
Makale Türü Açık Erişim Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY (Q2)
Dergi ISSN 1095-6670 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili Türkçe Basım Tarihi 08-2025
Cilt / Sayı / Sayfa 39 / 8 / 1–10 DOI 10.1002/jbt.70366
Makale Linki https://doi.org/10.1002/jbt.70366
Özet
Paracetamol (acetaminophen) is a widely used analgesic and antipyretic drug. Although many studies are available showing that paracetamol causes hepatic damage, few studies exist on renal damage. Protein tyrosine phosphatase receptor type O (PTPRO) protein has tyrosine phosphatase activity and plays a role in the regulation of the renal glomerular pressure/filtration rate relationship in podocyte structure. The PTPRO gene also exhibits characteristics of a candidate tumor suppressor gene. In this study, apoptosis, cell cycle, colony formation, and PTPRO gene expression of the human embryonic kidney (HEK 293) cells were assessed by treating with paracetamol at different concentrations for 24 and 26 h in at least three independent trials. Paracetamol induced dose‐dependent apoptosis at all concentrations (5, 10, 15, 20, and 30 mM) for both 24 and 26 h (p < 0.05–p < 0.001). Paracetamol …
Anahtar Kelimeler
acetaminophen (paracetamol) | apoptosis | cell cycle | colony formation | HEK 293 cells | PTPRO | renal cancer