Fucoidan Inhibits Prostate Cancer Growth Through Modulation of Different Cell Deaths

被引:0
|
作者
Tutuncu, M. [1 ]
Sanlav, G. [1 ]
Aktas, S. [1 ]
Yilmaz, O. [2 ]
Altun, Z. S. [1 ]
机构
[1] Dokuz Eylul Univ, Inst Oncol, Dept Basic Oncol, Izmir, Turkiye
[2] Dokuz Eylul Univ, Inst Hlth Sci, Dept Anim Sci, Izmir, Turkiye
关键词
Cell death; docetaxel; fucoidan; xenograft prostate cancer model; DOCETAXEL; APOPTOSIS; AUTOPHAGY;
D O I
10.4103/njcp.njcp_512_23
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background:Docetaxel (DOC) is the main chemotherapeutic agent for the treatment of advanced metastatic prostate cancer. Docetaxel shows anticancer effects by preventing the depolymerization of microtubules in the cell, therefore preventing cell division. However, the low survival effect of docetaxel has prompted researchers to search for novel therapeutic agents. Fucoidan (FUC) is a sulfated polysaccharide derived from brown algae. It has many bioactivities which makes fucoidan a promising anticancer agent. In this study, the potential anti-tumorigenic and preventive effects of fucoidan with or without docetaxel in prostate cancer were investigated by analyzing different cell death modalities.Methods:The in-vivo six groups (n = 8) were conducted; preventive (Pt), docetaxel treated after preventive (Pt-D), control, fucoidan (FUC), docetaxel (DOC), and FUC and DOC (FUC+DOC) combination. Apoptotic, necroptotic, and autophagic cell death-related protein expressions were assessed in tumor tissues by using immunohistochemical staining. Oxidative stress-related lipid peroxidation, glutathione peroxidase, and glutathione levels were also determined in tumor tissues.Results:Although apoptotic, necroptotic, and autophagic cell deaths were significantly induced in agent-treated groups compared to the control. Apoptotic cell death was more significantly induced in FUC and FUC+DOC-treated groups. Necroptotic cell death was increased considerably by inducing MLKL protein expression in all treatment groups. In the FUC, Pt, and DOC groups, LC3A/B expressions were significantly increased. DOC, FUC+DOC, and Pt-D treatments caused a significant increase in Beclin-1 expression. Oxidative stress-related MDA, GPX, and GSH levels significantly decreased with FUC treatment. The anti-tumorigenic effects of FUC and DOC were also demonstrated through tumor size reduction.Conclusion:According to the findings of this study, FUC inhibited tumor growth temporally and dimensionally, especially in preventive applications. FUC and FUC+DOC combinations in both treatment groups showed anti-tumorigenic effects. The results of this study suggest that fucoidan is a promising anticancer agent against prostate cancer. FUC can be considered as a preventive or treatment agent in prostate cancer therapy with DOC. Further studies are needed to fully elucidate the mechanism of action of fucoidan in metastatic prostate cancer.
引用
收藏
页码:827 / 836
页数:10
相关论文
共 50 条
  • [41] Inhibition of lewis lung cancer cell growth and migration by fucoidan
    Han, Yong-seok
    Lee, Jun Hee
    Chang, Hun Soo
    Lee, Sang Hun
    MOLECULAR & CELLULAR TOXICOLOGY, 2014, 10 (03) : 269 - 276
  • [42] Trichomonas Vaginalis Inhibits HeLa Cell Growth Through Modulation of Critical Molecules for Cell Proliferation and Apoptosis
    Zhu, Ziwen
    Zhao, Lei
    Brittingham, Andrew
    Bai, Qian
    Wakefield, Mark R.
    Fang, Yujiang
    ANTICANCER RESEARCH, 2018, 38 (09) : 5079 - 5086
  • [43] Modulation of prostate cancer growth in bone microenvironments
    Edlund, M
    Sung, SY
    Chung, LWK
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2004, 91 (04) : 686 - 705
  • [44] Androgens Promote Prostate Cancer Cell Growth through Induction of Autophagy
    Shi, Yan
    Han, Jenny J.
    Tennakoon, Jayantha B.
    Mehta, Fabiola F.
    Merchant, Fatima A.
    Burns, Alan R.
    Howe, Matthew K.
    McDonnell, Donald P.
    Frigo, Daniel E.
    MOLECULAR ENDOCRINOLOGY, 2013, 27 (02) : 280 - 295
  • [45] Chinese red yeast rice extract inhibits androgen-dependent and independent prostate cancer cell growth but by different mechanisms
    Hong, Mee Young
    Seeram, Navindra
    Zhang, Yanjun
    Heber, David
    FASEB JOURNAL, 2007, 21 (05): : A364 - A364
  • [46] Gossypol inhibits the growth of MAT-LyLu prostate cancer cells by modulation of TGFβ/Akt signaling
    Jiang, Jiahua
    Ye, Weiping
    Lin, Young C.
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2009, 24 (01) : 69 - 75
  • [47] Bortezomib inhibits cell proliferation in prostate cancer
    Zheng, Ren-Ping
    Wang, Wei
    Wei, Chuan-Dong
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2015, 10 (03) : 1219 - 1223
  • [48] Kartogenin Inhibits Prostate Cancer Cell Growth Through Smad2 Activation and Decreases Androgen Receptor Nuclear Localization
    Takai, Manabu
    Kawakami, Kyojiro
    Fujita, Yasunori
    Kato, Taku
    Kato, Daiki
    Iinuma, Koji
    Koie, Takuya
    Ito, Masafumi
    Mizutani, Kosuke
    ANTICANCER RESEARCH, 2021, 41 (10) : 4753 - 4759
  • [49] Vitamin E plus C inhibits survivin and human prostate cancer cell growth
    Meikle, AW
    Campbell, LD
    Gunawardena, K
    JOURNAL OF INVESTIGATIVE MEDICINE, 2004, 52 (01) : S99 - S100
  • [50] Phosphoglycerate mutase 1 knockdown inhibits prostate cancer cell growth, migration, and invasion
    Wen, Yao-An
    Zhou, Bo-Wei
    Lv, Dao-Jun
    Shu, Fang-Peng
    Song, Xian-Lu
    Huang, Bin
    Wang, Chong
    Zhao, Shan-Chao
    ASIAN JOURNAL OF ANDROLOGY, 2018, 20 (02) : 178 - 183