Addition of docosahexaenoic acid synergistically enhances the efficacy of apatinib for triple-negative breast cancer therapy

被引:12
作者
Ma, Yingjie [1 ]
Yu, Junxian [2 ]
Li, Qin [1 ]
Su, Qiang [1 ]
Cao, Bangwei [1 ]
机构
[1] Capital Med Univ, Beijing Friendship Hosp, Canc Ctr, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Friendship Hosp, Dept Pharm, Beijing, Peoples R China
基金
北京市自然科学基金;
关键词
Akt; breast tumor; targeted molecular therapy; apatinib; docosahexaenoic acid; ENDOTHELIAL-GROWTH-FACTOR; POLYUNSATURATED FATTY-ACIDS; CELL-PROLIFERATION; PHASE-II; INHIBITOR APATINIB; FACTOR RECEPTOR-2; TUMOR-GROWTH; ANGIOGENESIS; APOPTOSIS; COMBINATION;
D O I
10.1080/09168451.2019.1709789
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The current study aimed to investigate the antitumor and antiangiogenesis effects of apatinib in triple-negative breast cancer in vitro and also whether the combination of docosahexaenoic acid (DHA) and apatinib is more effective than apatinib monotherapy. The cell counting kit-8 assay was used to measure cell proliferation. Flow cytometry was utilized to determine the cell apoptosis rate. A wound healing assay was utilized to assess cell migration. Western blot analysis was carried out to determine the effects of apatinib and DHA on Bcl-2, BAX, cleaved caspase-3, caspase-3, phosphorylated protein kinase B (p-Akt), and Akt expression. DHA in combination with apatinib showed enhanced inhibitory effects on cell proliferation and migration compared with apatinib or DHA monotherapy. Meanwhile, DHA combined with apatinib strongly increased the cell apoptosis percentage. DHA was observed to enhance the antitumor and antiangiogenesis effects of apatinib via further downregulation of p-Akt expression.
引用
收藏
页码:743 / 756
页数:14
相关论文
共 50 条
[21]   Novel therapy for locally advanced triple-negative breast cancer [J].
Yamada, Atsuko ;
Osada, Shinji ;
Tanahashi, Toshiyuki ;
Matsui, Satoshi ;
Sasaki, Yoshiyuki ;
Tanaka, Yoshihiro ;
Okumura, Naoki ;
Matsuhashi, Nobuhisa ;
Takahashi, Takao ;
Yamaguchi, Kazuya ;
Yoshida, Kazuhiro .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2015, 47 (04) :1266-1272
[22]   A case report of low-dose apatinib in the treatment of advanced triple-negative breast cancer [J].
Lv, Ye ;
Zhang, Huiqiang ;
Zhao, Yanjiao ;
Zhang, Haixia ;
Wang, Tao .
TRANSLATIONAL BREAST CANCER RESEARCH, 2024, 5
[23]   A review of current progress in triple-negative breast cancer therapy [J].
Shen, Meiying ;
Pan, Huawen ;
Chen, Yuxia ;
Xu, Yu Hang ;
Yang, Weixiong ;
Wu, Zhaojun .
OPEN MEDICINE, 2020, 15 (01) :1143-1149
[24]   Anticancer Effects of Nervonic Acid in Triple-Negative Breast Cancer [J].
Kawai, Akiho ;
Ono, Fumiaki ;
Satou, Takao ;
Itoh, Tatsuki .
JOURNAL OF OLEO SCIENCE, 2025, 74 (04) :409-421
[25]   A fatty acid-binding protein 7/RXRβ pathway enhances survival and proliferation in triple-negative breast cancer [J].
Liu, Rong-Zong ;
Graham, Kathryn ;
Glubrecht, Darryl D. ;
Lai, Raymond ;
Mackey, John R. ;
Godbout, Roseline .
JOURNAL OF PATHOLOGY, 2012, 228 (03) :310-321
[26]   Metastatic Triple-negative Breast Cancer [J].
Rakha, E. A. ;
Chan, S. .
CLINICAL ONCOLOGY, 2011, 23 (09) :587-600
[27]   Efficacy of Sequential Capecitabine on Adjuvant Chemotherapy of Triple-Negative Breast Cancer [J].
Xi, Xun ;
Huang, Xingwei ;
Yuan, Huozhong ;
Ni, Jun ;
Yang, Fulan .
JOURNAL OF HEALTHCARE ENGINEERING, 2022, 2022
[28]   Efficacy and safety of anlotinib for triple-negative breast cancer with brain metastases [J].
Liu, Zeyu ;
Li, Ming ;
Zhao, Ziyi ;
Liu, Aina ;
Sun, Ping .
FRONTIERS IN ONCOLOGY, 2024, 14
[29]   PRKCQ inhibition enhances chemosensitivity of triple-negative breast cancer by regulating Bim [J].
Jessica H. Byerly ;
Elisa R. Port ;
Hanna Y. Irie .
Breast Cancer Research, 22
[30]   PRKCQ inhibition enhances chemosensitivity of triple-negative breast cancer by regulating Bim [J].
Byerly, Jessica H. ;
Port, Elisa R. ;
Irie, Hanna Y. .
BREAST CANCER RESEARCH, 2020, 22 (01)