Comparative Cytotoxicity of Artemisinin and Cisplatin and Their Interactions with Chlorogenic Acids in MCF7 Breast Cancer Cells

被引:71
|
作者
Suberu, John O. [2 ]
Romero-Canelon, Isolda [3 ]
Sullivan, Neil [4 ]
Lapkin, Alexei A. [2 ]
Barker, Guy C. [1 ]
机构
[1] Univ Warwick, Sch Life Sci, Coventry CV4 7AL, W Midlands, England
[2] Univ Cambridge, Cambridge CB2 3RA, England
[3] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
[4] SensaPharm Ltd, Biosci Ctr 123I, Sunderland SR5 2TA, England
基金
英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会;
关键词
antagonism; Artemisia tea; artemisinin; chlorogenic acid; cisplatin; synergy; ANNUA TEA INFUSION; IN-VITRO; ANTIMALARIAL ACTIVITY; CAFFEIC ACID; HERBAL TEA; QING-HAO; ARTESUNATE; POLYPHENOLS; RESISTANCE; INHIBITION;
D O I
10.1002/cmdc.201402285
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In parts of Africa and Asia, self-medication with a hot water infusion of Artemisia annua (Artemisia tea) is a common practice for a number of ailments including malaria and cancer. In our earlier work, such an extract showed better potency than artemisinin alone against both chloroquine-sensitive and -resistant parasites. In this study, in vitro tests of the infusion in MCF7 cells showed high IC50 values (>200M). The combination of artemisinin and 3-caffeoylquinic acid (3CA), two major components in the extract, was strongly antagonistic and gave a near total loss of cytotoxicity for artemisinin. We observed that the interaction of 3CAs with another cytotoxic compound, cisplatin, showed potentiation of activity by 2.5-fold. The chelation of cellular iron by 3CA is hypothesized as a possible explanation for the loss of artemisinin activity.
引用
收藏
页码:2791 / 2797
页数:7
相关论文
共 50 条
  • [31] COMPARATIVE LOCALIZATION OF RECEPTORS FOR PLASMIN AND FOR UROKINASE ON MCF7 CELLS
    ZHANG, S
    LAURENT, M
    LOPEZALEMANY, R
    MAZAR, A
    HENKIN, J
    RONNE, E
    BURTIN, P
    EXPERIMENTAL CELL RESEARCH, 1993, 207 (02) : 290 - 299
  • [32] Christia vespertilionis extract induced antiproliferation and apoptosis in breast cancer (MCF7) cells
    Ismail, Noor Zafirah
    Adebayo, Ismail Abiola
    Mohamed, Wan Ahmad Syazani
    Mohamad Zain, Nur Nadhirah
    Arsad, Hasni
    MOLECULAR BIOLOGY REPORTS, 2021, 48 (11) : 7361 - 7370
  • [33] Transcription Regulation Network Analysis of MCF7 Breast Cancer Cells Exposed to Estradiol
    Wu, Jun-Zhao
    Lu, Peng
    Liu, Rong
    Yang, Tie-Jian
    ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2012, 13 (08) : 3681 - 3685
  • [34] Direct and indirect P-glycoprotein transfers in MCF7 breast cancer cells
    Dyson, Janet
    Le Foll, Frank
    Magal, Pierre
    Noussair, Ahmed
    Pasquier, Jennifer
    JOURNAL OF THEORETICAL BIOLOGY, 2019, 461 : 239 - 253
  • [35] The Effect of Menadione and Vitamin D on MCF7 Breast Cancer
    Carlson, Clayton
    Briscoe, Emily
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2024, 300 (03) : S571 - S571
  • [36] Inhibitory effects of probiotic Bacillus coagulans against MCF7 breast cancer cells
    Dolati, Masoumeh
    Tafvizi, Farzaneh
    Salehipour, Masoud
    Movahed, Tahereh Komeili
    Jafari, Parvaneh
    IRANIAN JOURNAL OF MICROBIOLOGY, 2021, 13 (06) : 839 - 847
  • [37] Christia vespertilionis extract induced antiproliferation and apoptosis in breast cancer (MCF7) cells
    Noor Zafirah Ismail
    Ismail Abiola Adebayo
    Wan Ahmad Syazani Mohamed
    Nur Nadhirah Mohamad Zain
    Hasni Arsad
    Molecular Biology Reports, 2021, 48 : 7361 - 7370
  • [38] Adiponectin mediates antiproliferative and apoptotic responses in human MCF7 breast cancer cells
    Dieudonne, Marie-Noelle
    Bussiere, Marianne
    Dos Santos, Esther
    Leneveu, Marie-Christine
    Giudicelli, Yves
    Pecquery, Rene
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 345 (01) : 271 - 279
  • [39] Chronic cadmium exposure decreases the dependency of MCF7 breast cancer cells on ERα
    Mathew Bloomfield
    Maggie C. Louie
    Scientific Reports, 9
  • [40] Azacytidine-induced Chemosensitivity to Doxorubicin in Human Breast Cancer MCF7 Cells
    Khan, Gul Nabi
    Kim, Eun Jin
    Shin, Tae Seop
    Lee, Sang Ho
    ANTICANCER RESEARCH, 2017, 37 (05) : 2355 - 2364