Effects of electroporation on anticancer activity of 5-FU and newly synthesized zinc(II) complex in chemotherapy-resistance human brain tumor cells

Autor: Sevgi Irtegun Kandemir, Yusuf Alan, Nevin Turan, Kenan Buldurun, Mehmet Esref Alkis
Přispěvatelé: Dicle Üniversitesi, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyoloji Ana Bilim Dalı, Kandemir, Sevgi İrtegün
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Cancer Research
Electrochemotherapy
antineoplastic metal complex
Zn(II) complex
IC50
fluorescence microscopy
Anticancer activity
fluorouracil
zinc 4 (2 hydroxybenzylideneamino)pyrimidin 2(1h) one
Cytotoxic T cell
Cytotoxicity
cancer resistance
antineoplastic agent
MTT assay
T98G cell line
Chemistry
Brain Neoplasms
Electroporation
drug cytotoxicity
Hematology
General Medicine
unclassified drug
Oncology
U-118MG cell line
cytotoxic agent
polymerization
skin fibroblast
brain tumor
electroporation
zinc derivative
5-Fluorouracil
Spectral techniques
chemistry.chemical_element
Antineoplastic Agents
Zinc
antineoplastic activity
chemistry
Article
Dermal fibroblast
Cell Line
Tumor

Humans
controlled study
human
cell viability
drug resistance
human cell
glioblastoma
tumor cell line
Molecular biology
cell proliferation
Cell culture
Drug Resistance
Neoplasm

Zinc Compounds
drug synthesis
pathology
Popis: Zn(II) complex of Schiff base derived from the condensation of 4-aminopyrimidine-2(1H)-one with salicylaldehyde was prepared and characterized by various physico‐chemical and spectral methods for structure determination. The cytotoxic activity of the Zn(II) complex was investigated in comparison with 5-fluorouracil (5-FU) against two different human brain tumor cell lines (T98G and U118), while primer human dermal fibroblast cells (HDF) was used as control for biocompatibility. Then, the effectiveness of electroporation (EP) on cytotoxic activities of these compounds has been examined. The cytotoxicities of the 5-FU and new Zn(II) complex, alone or in combination with electroporation, were determined by MTT assay. The Zn(II) complex showed good cytotoxicity against T98G and U118 brain tumor cell lines with IC50 = 282.47 and 297.91 μM respectively, while it was safe on HDF healthy cells with IC50 = 826.72 μM. The 5-FU exhibited less cytotoxicity compared to the Zn(II) complex against T98G (IC50 = 382.35 μM) and U118 (IC50 = 396.56 μM) tumor cell lines. The combined application of Zn (II) + EP decreased the IC50 value by 5.96-fold in T98G cells and 4.76-fold in U118 cells. EP showed a similar effect in its combined application with 5-FU, resulting in a decrease of the IC50 value of 4.22-fold in the T98G cells and 3.84-fold in the U118 cells. In a conclusion, the Zn(II) complex exhibited an anticancer potential against both brain tumor cell lines (T98G and U118) and EP greatly increased the cytotoxicity of Zn(II) complex and 5-FU on these chemotherapy-resistant cells.
Databáze: OpenAIRE