Urushiol V Suppresses Cell Proliferation and Enhances Antitumor Activity of 5-FU in Human Colon Cancer Cells by Downregulating FoxM1

被引:5
作者
Jeong, Ji Hye
Ryu, Jae-Ha [1 ]
机构
[1] Sookmyung Womens Univ, Res Inst Pharmaceut Sci, Seoul 04310, South Korea
基金
新加坡国家研究基金会;
关键词
Urushiol V; FoxM1; Colorectal cancer; 5-FU; Drug resistance; Antitumor; RHUS-VERNICIFLUA STOKES; THYMIDYLATE SYNTHASE; TRANSCRIPTION FACTOR; 5-FLUOROURACIL RESISTANCE; COLORECTAL-CANCER; CERVICAL-CANCER; EXPRESSION; PROGRESSION; INVASION; AMPK;
D O I
10.4062/biomolther.2022.008
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
Colorectal cancer (CRC) is one of the most common malignant tumor. 5-FU is commonly used for the treatment of CRC. However, the development of drug resistance in tumor chemotherapy can seriously reduce therapeutic efficacy of 5-FU. Recent data show that FoxM1 is associated with 5-FU resistance in CRC. FoxM1 plays a critical role in the carcinogenesis and drug resistance of several malignancies. It has been reported that urushiol V isolated from the cortex of Rhus verniciflua Stokes is cytotoxic to several types of cancer cells. However, the underlying molecular mechanisms for its antitumor activity and its potential to attenuate the chemotherapeutic resistance in CRC cells remain unknown. Here, we found that urushiol V could inhibit the cell proliferation and induced S-phase arrest of SW480 colon cancer cells. It inhibited protein expression level of FoxM1 through activation of AMPK. We also investigated the combined effect of urushiol V and 5-FU. The combination treatment reduced FoxM1 expression and consequently reduced cell growth and colony formation in 5-FU resistant colon cancer cells (SW480/5-FUR). Taken together, these result suggest that urushiol V from Rhus verniciflua Stokes can suppress cell proliferation by inhibiting FoxM1 and enhance the antitumor capacity of 5-FU. Therefore, urushiol V may be a potential bioactive compound for CRC therapy.
引用
收藏
页码:257 / 264
页数:8
相关论文
共 50 条
  • [1] Annexin A1 is involved in resistance to 5-FU in colon cancer cells
    Onozawa, Hisashi
    Saito, Motonobu
    Saito, Katsuharu
    Kanke, Yasuyuki
    Watanabe, Yohei
    Hayase, Suguru
    Sakamoto, Wataru
    Ishigame, Teruhide
    Momma, Tomoyuki
    Ohki, Shinji
    Takenoshita, Seiichi
    ONCOLOGY REPORTS, 2017, 37 (01) : 235 - 240
  • [2] Knockdown of FOXM1 suppresses cell growth and metastasis in human laryngeal cancer via the AKT signaling pathway
    Yan, J.
    Hou, J.
    Yan, Y.
    Ren, X-Y
    Luo, H-N
    Wang, Z-G
    Zheng, G-X
    EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES, 2020, 24 (12) : 6786 - 6793
  • [3] FOXM1/NCAPH activates glycolysis to promote colon adenocarcinoma stemness and 5-FU resistance
    Lei, Yuehua
    Wang, Dengchao
    Chen, Wenxing
    Tian, Xiaojun
    Wei, Jian
    ANTI-CANCER DRUGS, 2023, 34 (08) : 929 - 938
  • [4] Epigenetically modulated FOXM1 suppresses dendritic cell maturation in pancreatic cancer and colon cancer
    Zhou, Zhongshi
    Chen, Hongdan
    Xie, Rui
    Wang, Hongjie
    Li, Senlin
    Xu, Qianqian
    Xu, Na
    Cheng, Qi
    Qian, Ying
    Huang, Rongrong
    Shao, Zekun
    Xiang, Ming
    MOLECULAR ONCOLOGY, 2019, 13 (04) : 873 - 893
  • [5] miR-342-3p suppresses proliferation, migration and invasion by targeting FOXM1 in human cervical cancer
    Li, Xu-ri
    Chu, Hui-jun
    Lv, Teng
    Wang, Lei
    Kong, Shou-fang
    Dai, Shu-zhen
    FEBS LETTERS, 2014, 588 (17): : 3298 - 3307
  • [6] miR-877-5p Suppresses Gastric Cancer Cell Proliferation Through Targeting FOXM1
    Wu, Kun
    Yu, Zhu
    Tang, Zhenyong
    Wei, Weiyuan
    Xie, Dongyi
    Xie, Yubo
    Xiao, Qiang
    ONCOTARGETS AND THERAPY, 2020, 13 : 4731 - 4742
  • [7] miR-320 enhances the sensitivity of human colon cancer cells to chemoradiotherapy in vitro by targeting FOXM1
    Wan, Lu-Ying
    Deng, Jun
    Xiang, Xiao-Jun
    Zhang, Ling
    Yu, Feng
    Chen, Jun
    Sun, Zhe
    Feng, Miao
    Xiong, Jian-Ping
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2015, 457 (02) : 125 - 132
  • [8] FOXM1 modulates 5-FU resistance in colorectal cancer through regulating TYMS expression
    Varghese, Vidhya
    Magnani, Luca
    Harada-Shoji, Narumi
    Mauri, Francesco
    Szydlo, Richard M.
    Yao, Shang
    Lam, Eric W. -F.
    Kenny, Laura M.
    SCIENTIFIC REPORTS, 2019, 9 (1)
  • [9] Short hairpin RNA- mediated gene knockdown of FOXM1 inhibits the proliferation and metastasis of human colon cancer cells through reversal of epithelial-to-mesenchymal transformation
    Yang, KanKan
    Jiang, LinHua
    Hu, You
    Yu, Jing
    Chen, HenFeng
    Yao, YiZhou
    Zhu, XinGuo
    JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2015, 34
  • [10] Overcoming 5-Fu resistance in human non-small cell lung cancer cells by the combination of 5-Fu and cisplatin through the inhibition of glucose metabolism
    Zhao, Jun-gang
    Ren, Kai-ming
    Tang, Jun
    TUMOR BIOLOGY, 2014, 35 (12) : 12305 - 12315