Synergistic effect between celecoxib and luteolin is dependent on estrogen receptor in human breast cancer cells

被引:29
作者
Jeon, Ye Won [1 ]
Ahn, Young Ee [2 ]
Chung, Won Sang [2 ]
Choi, Hyun Joo [3 ]
Suh, Young Jin [1 ]
机构
[1] Catholic Univ Korea, St Vincents Hosp, Dept Surg, Coll Med, Suwon 442723, Kyounggi Do, South Korea
[2] Catholic Univ Korea, St Vincents Hosp, Dept Radiol, Coll Med, Suwon 442723, Kyounggi Do, South Korea
[3] Catholic Univ Korea, St Vincents Hosp, Dept Pathol, Coll Med, Suwon 442723, Kyounggi Do, South Korea
关键词
Breast neoplasms; Celecoxib; Luteolin; Apoptosis; Estrogen; Receptors; ACTIVATED PROTEIN-KINASE; INDUCED APOPTOSIS; CYCLOOXYGENASE-2; INHIBITOR; DOWN-REGULATION; MESSENGER-RNA; EXPRESSION; PATHWAY; TARGET; COX-2; MODEL;
D O I
10.1007/s13277-015-3322-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The anti-cancer effects of celecoxib and luteolin are well known. Although our previous study demonstrated that the combination of celecoxib and luteolin synergistically inhibits breast tumor growth compared with each of the treatments alone, we did not uncover the molecular mechanisms of these effects. The aims of our present study were to compare the effects of a celecoxib and luteolin combination treatment in four different human breast cell lines and to determine the mechanisms of action in vitro and in vivo. The synergistic effects of a celecoxib and luteolin combination treatment yielded significantly greater cell growth inhibition in all four breast cancer cell lines compared with the single agents alone. In particular, combined celecoxib and luteolin treatment significantly decreased the growth of MDA-MB-231 cancer cells in vivo compared with either agent alone. The celecoxib and luteolin combination treatment induced synergistic effects via Akt inactivation and extracellular signal-regulated kinase (ERK) signaling inhibition in MCF-7 and MCF7/HER18 cells and via Akt inactivation and ERK signaling activation in MDA-MB-231 and SkBr3 cells. These results demonstrate the synergistic anti-tumor effect of the celecoxib and luteolin combination treatment in different four breast cancer cell lines, thus introducing the possibility of this combination as a new treatment modality.
引用
收藏
页码:6349 / 6359
页数:11
相关论文
共 50 条
  • [21] Sulforaphane-induced metabolomic responses with epigenetic changes in estrogen receptor positive breast cancer cells
    Cao, Shuyuan
    Wang, Li
    Zhang, Zhan
    Chen, Feng
    Wu, Qian
    Li, Lei
    FEBS OPEN BIO, 2018, 8 (12): : 2022 - 2034
  • [22] Effect of estrogen on telomerase activity in human breast cancer cells
    Gao Jinbo
    Chen Daoda
    Tian Yuan
    Zhang Jinhui
    Cai Kailin
    Current Medical Science, 2003, 23 (3) : 286 - 287
  • [23] Effect of Estrogen on Telomerase Activity in Human Breast Cancer Cells
    高金波
    陈道达
    田元
    张锦辉
    蔡开琳
    华中科技大学学报(医学英德文版), 2003, (03) : 286 - 287
  • [24] Estrogen, Progesterone, and HER-2 Receptor Immunostaining in Cytology: The Effect of Varied Fixation on Human Breast Cancer Cells
    Maleki, Sara
    Dorokhova, Olena
    Sunkara, Jaya
    Schlesinger, Kathie
    Suhrland, Mark
    Oktay, Maja H.
    DIAGNOSTIC CYTOPATHOLOGY, 2013, 41 (10) : 864 - 870
  • [25] Interaction of celecoxib with different anti-cancer drugs is antagonistic in breast but not in other cancer cells
    El-Awady, Raafat A.
    Saleh, Ekram M.
    Ezz, Marwa
    Elsayed, Abeer M.
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 2011, 255 (03) : 271 - 286
  • [26] The effect of celecoxib on tumor growth in ovarian cancer cells and a genetically engineered mouse model of serous ovarian cancer
    Suri, Anuj
    Sheng, Xiugui
    Schuler, Kevin M.
    Zhong, Yan
    Han, Xiaoyun
    Jones, Hannah M.
    Gehrig, Paola A.
    Zhou, Chunxiao
    Bae-Jump, Victoria L.
    ONCOTARGET, 2016, 7 (26) : 39582 - 39594
  • [27] Effect of Estrogen on Heteronemin-Induced Anti-proliferative Effect in Breast Cancer Cells With Different Estrogen Receptor Status
    Yang, Yu-Chen S. H.
    Li, Zi-Lin
    Huang, Tung-Yung
    Su, Kuan-Wei
    Lin, Chi-Yu
    Huang, Chi-Hung
    Chen, Han-Yu
    Lu, Mei-Chin
    Huang, Haw-Ming
    Lee, Sheng-Yang
    Whang-Peng, Jaqueline
    Lin, Hung-Yun
    Davis, Paul J.
    Wang, Kuan
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2021, 9
  • [28] Estrogen stimulated migration and invasion of estrogen receptor-negative breast cancer cells involves an ezrin-dependent crosstalk between G protein-coupled receptor 30 and estrogen receptor beta signaling
    Zhou, Kewen
    Sun, Peng
    Zhang, Yaxing
    You, Xinchao
    Li, Ping
    Wang, Tinghuai
    STEROIDS, 2016, 111 : 113 - 120
  • [29] Silencing estrogen receptor α in breast cancer cells
    Zhou, Qun
    Davidson, Nancy E.
    CANCER BIOLOGY & THERAPY, 2006, 5 (07) : 848 - 849
  • [30] Resveratrol enhances the chemopreventive effect of celecoxib in chemically induced breast cancer in rats
    Kiskova, Terezia
    Jendzelovsky, Rastislav
    Rentsen, Erdenetsetsek
    Maier-Salamon, Alexandra
    Kokosova, Natalia
    Papcova, Zuzana
    Mikes, Jaromir
    Orendas, Peter
    Bojkova, Bianka
    Kubatka, Peter
    Svoboda, Martin
    Kajo, Karol
    Fedorocko, Peter
    Jaeger, Walter
    Ekmekcioglu, Cem
    Kassayova, Monika
    Thalhammer, Theresia
    EUROPEAN JOURNAL OF CANCER PREVENTION, 2014, 23 (06) : 506 - 513