Syringic acid induces cancer cell death in the presence of Cu (II) ions via pro-oxidant activity

被引:2
|
作者
Rashedinia, Marzieh [1 ,2 ]
Nasrollahi, Azita [2 ]
Shafaghat, Marzieh [2 ]
Momeni, Shahrzad [2 ]
Iranpak, Forough [3 ,4 ]
Saberzadeh, Jamileh [3 ]
Arabsolghar, Rita [3 ,5 ]
Sabahi, Zahra [1 ]
机构
[1] Shiraz Univ Med Sci, Med Plants Proc Res Ctr, Shiraz, Iran
[2] Shiraz Univ Med Sci, Fac Pharm, Dept Pharmacol & Toxicol, Shiraz, Iran
[3] Shiraz Univ Med Sci, Diagnost Lab Sci & Technol Res Ctr, Sch Paramed Sci, Shiraz, Iran
[4] Islamic Azad Univ Shiraz, Dept Biochem, Shiraz, Iran
[5] Shiraz Univ Med Sci, Sch Paramed Sci, Dept Med Lab Sci, Shiraz, Iran
关键词
Syringic acid; Copper; Iron; Cancer cell; Pro-oxidant; Autophagy; OXIDATIVE STRESS; HYDROGEN-PEROXIDE; DNA PROTECTION; COPPER; MECHANISM; AUTOPHAGY; ANTIOXIDANT; POLYPHENOLS; APOPTOSIS; TOXICITY;
D O I
10.4103/2221-1691.345519
中图分类号
R188.11 [热带医学];
学科分类号
摘要
Objective: To investigate the effects of syringic acid on HEK 293 and HepG2 cells in the absence and presence of exogenous Cu (II) and Fe (II) ions. Methods: The antiproliferative effects of syringic acid on HEK 293 and HepG2 cells in the absence and presence of exogenous Cu (II) and Fe (II) ions were examined by MTT assay. Additionally, colony-forming, reactive oxidative species (ROS) generation, apoptosis induction, autophagy, mitochondrial membrane potential, and mitochondrial mass were investigated. Results: At 24 and 72 h, no significant differences were observed in the viability of HepG2 cells between the control and syringic acid + Fe (II) groups. However, exposure of HepG2 cells to syringic acid + Cu (II) for 72 h reduced the cell viability significantly. Furthermore, ROS formation, induction of apoptosis, and autophagic vacuoles were significantly increased in HepG2 cells without marked changes in mitochondrial membrane potential and mitochondrial mass. Moreover, syringic acid + Cu (II) reduced the plating efficiency and surviving fraction significantly. Conclusions: The combination of syringic acid with Cu (II) was toxic to cancer cells and showed pro-oxidant activity. In addition, this combination induced autophagy in cancer cells with less cytotoxic effects on normal cells, which is a potential candidate for the development of novel therapeutics towards cancer.
引用
收藏
页码:270 / 278
页数:9
相关论文
共 44 条
  • [21] The pro-inflammatory oxidant hypochlorous acid induces Bax-dependent mitochondrial permeabilisation and cell death through AIF-/EndoG-dependent pathways
    Whiteman, Matthew
    Chu, Siew Hwa
    Siau, Jia Ling
    Rose, Peter
    Sabapathy, Kanaga
    Schantz, Jan-Thorsten
    Cheung, Nam Sang
    Spencer, Jeremy P. E.
    Armstrong, Jeffrey S.
    CELLULAR SIGNALLING, 2007, 19 (04) : 705 - 714
  • [22] Simulating hypoxia-induced acidic environment in cancer cells facilitates mobilization and redox-cycling of genomic copper by daidzein leading to pro-oxidant cell death: implications for the sensitization of resistant hypoxic cancer cells to therapeutic challenges
    Ullah, Mohammad F.
    Ahmad, Aamir
    Bhat, Showket H.
    Khan, Husain Y.
    Zubair, Haseeb
    Sarkar, Fazlul H.
    Hadi, Sheikh M.
    BIOMETALS, 2016, 29 (02) : 299 - 310
  • [23] Simulating hypoxia-induced acidic environment in cancer cells facilitates mobilization and redox-cycling of genomic copper by daidzein leading to pro-oxidant cell death: implications for the sensitization of resistant hypoxic cancer cells to therapeutic challenges
    Mohammad F. Ullah
    Aamir Ahmad
    Showket H. Bhat
    Husain Y. Khan
    Haseeb Zubair
    Fazlul H. Sarkar
    Sheikh M. Hadi
    BioMetals, 2016, 29 : 299 - 310
  • [24] Gambogic acid inhibits thioredoxin activity and induces ROS-mediated cell death in castration-resistant prostate cancer
    Pan, Hong
    Jansson, Keith H.
    Beshiri, Michael L.
    Yin, JuanJuan
    Fang, Lei
    Agarwal, Supreet
    Nguyen, Holly
    Corey, Eva
    Zhang, Ying
    Liu, Jie
    Fan, HuiTing
    Lin, HongSheng
    Kelly, Kathleen
    ONCOTARGET, 2017, 8 (44) : 77181 - 77194
  • [25] The n3-polyunsaturated fatty acid docosahexaenoic acid induces immunogenic cell death in human cancer cell lines via pre-apoptotic calreticulin exposure
    Romina Molinari
    Donatella D’Eliseo
    Laura Manzi
    Lello Zolla
    Francesca Velotti
    Nicolò Merendino
    Cancer Immunology, Immunotherapy, 2011, 60 : 1503 - 1507
  • [26] The n3-polyunsaturated fatty acid docosahexaenoic acid induces immunogenic cell death in human cancer cell lines via pre-apoptotic calreticulin exposure
    Molinari, Romina
    D'Eliseo, Donatella
    Manzi, Laura
    Zolla, Lello
    Velotti, Francesca
    Merendino, Nicolo
    CANCER IMMUNOLOGY IMMUNOTHERAPY, 2011, 60 (10) : 1503 - 1507
  • [27] Binuclear Cu(II) complex based on N-acetylanthranilic acid induces significant cytotoxic effect on three cancer cell lines
    Aly, Aref A. M.
    Zidan, Amna S. A.
    Ibrahim, Ahmed B. M.
    Mosbah, Hanan K.
    Mayer, Peter
    Saber, Saber H.
    JOURNAL OF MOLECULAR STRUCTURE, 2022, 1249
  • [28] Binuclear Cu(II) complex based on N-acetylanthranilic acid induces significant cytotoxic effect on three cancer cell lines
    Aly, Aref A.M.
    Zidan, Amna S.A.
    Ibrahim, Ahmed B.M.
    Mosbah, Hanan K.
    Mayer, Peter
    Saber, Saber H.
    Journal of Molecular Structure, 2022, 1249
  • [29] Pllans-II Induces Cell Death in Cervical Cancer Squamous Epithelial Cells via Unfolded Protein Accumulation and Endoplasmic Reticulum Stress
    Montoya-Gomez, Alejandro
    Rivera Franco, Nelson
    Ives Montealegre-Sanchez, Leonel
    Manuel Solano-Redondo, Luis
    Castillo, Andres
    Mosquera-Escudero, Mildrey
    Jimenez-Charris, Eliecer
    MOLECULES, 2022, 27 (19):
  • [30] Glutathione Depleting a Chemoselective Novel Pro-oxidant Nano Metal-Organic Framework Induced G2/M Arrest and ROS-Mediated Apoptotic Cell Death in a Human Triple-Negative Breast Cancer Cell Line
    Karim, Suhana
    Halder, Satyajit
    Mukherjee, Somali
    Debnath, Utsab
    Misra, Anup Kumar
    Jana, Kuladip
    Das, Debasis
    ACS APPLIED MATERIALS & INTERFACES, 2023, 15 (22) : 26442 - 26456