Co-downregulation of GRP78 and GRP94 induces apoptosis and inhibits migration in prostate cancer cells

被引:15
|
作者
Lu, Tong [1 ]
Wang, Yue [2 ]
Xu, Kang [1 ]
Zhou, Zhijun [1 ]
Gong, Juan [1 ]
Zhang, Yingang [1 ]
Gong, Hua [1 ]
Dai, Qiang [1 ]
Yang, Jun [1 ]
Xiong, Biao [1 ]
Song, Ze [1 ]
Yang, Gang [1 ]
机构
[1] First Peoples Hosp Tianmen City, Dept Urol, East 1,Renmin Ave, Tianmen City 431700, Hubei, Peoples R China
[2] Sinopharm Wuhan Plasma Derived Biotherapies Co Lt, 1 Attached 1,Zhengdian Gold Ind Pk Rd, Wuhan 430070, Hubei, Peoples R China
来源
OPEN LIFE SCIENCES | 2019年 / 14卷 / 01期
关键词
GRP78; GRP94; prostate cancer; apoptosis; migration; PROTEIN; METASTASIS; RESISTANCE; MECHANISMS; EXPRESSION; CHAPERONE; GROWTH; ROLES;
D O I
10.1515/biol-2019-0043
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Both glucose-regulated protein 78 kDa (GRP78) and glucose-regulated protein 94 kDa (GRP94) are important molecular chaperones that play critical roles in maintaining tumor survival and progression. This study investigated the effects in prostate cancer cells following the downregulation of GRP78 and GRP94. Methods: RNA interference was used to downregulate GRP78 and GRP94 expression in the prostate cancer cell line, PC-3. The effects on apoptosis and cell migration was examined along with expression of these related proteins. Results: Small interfering RNAs targeting GRP78 and GRP94 successfully downregulated their expression. This resulted in the induction of apoptosis and inhibition of cell migration. Preliminary mechanistic studies indicated that caspase-9 (cleaved) and Bax expression levels were upregulated while Bcl-2 and vimentin expression levels were downregulated. Conclusion: Co-downregulation of GRP78 and GRP94 expression induces apoptosis and inhibits migration in prostate cancer cells.
引用
收藏
页码:384 / 391
页数:8
相关论文
共 50 条
  • [31] ASSOCIATION OF HSP47, GRP78, AND GRP94 WITH PROCOLLAGEN SUPPORTS THE SUCCESSIVE OR COUPLED ACTION OF MOLECULAR CHAPERONES
    FERREIRA, LR
    NORRIS, K
    SMITH, T
    HEBERT, C
    SAUK, JJ
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 1994, 56 (04) : 518 - 526
  • [32] 不同训练状态大鼠心肌GRP78、GRP94和ERP72的表达
    史清钊
    陈怡月
    王智强
    李丁丁
    于海燕
    姚政立
    王蕴红
    [J]. 首都体育学院学报, 2018, 30 (03) : 268 - 271
  • [33] Inhibition of ICMT induces endothelial cell apoptosis through GRP94
    Lu, Qing
    Harrington, Elizabeth O.
    Newton, Julie
    Jankowich, Matthew
    Rounds, Sharon
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2007, 37 (01) : 20 - 30
  • [34] Overexpression of molecular chaperons GRP78 and GRP94 in CD44(h)i/CD24(lo) breast cancer stem cells
    Nami, Babak
    Ghasemi-Dizgah, Armin
    Vaseghi, Akbar
    [J]. BIOIMPACTS, 2016, 6 (02) : 105 - 110
  • [35] Lithium and valproate treatment increase the expression of the molecular chaperones GRP78, GRP94 and calreticulin in primary cultured rat cerebral cortical cells
    Shao, L
    Young, LT
    Wang, JF
    [J]. BIOLOGICAL PSYCHIATRY, 2003, 53 (08) : 141S - 141S
  • [36] Reduction of GRP78 increases expression of ATF4, GRP94, GADD153 in mIMCD3 cells.
    Tse, Jonathan
    Cai, Qi
    Weber, Craig
    Lynch, Ronald M.
    Brooks, Heddwen L.
    [J]. FASEB JOURNAL, 2009, 23
  • [37] GRP78-targeted nanotherapy against castrate-resistant prostate cancer cells expressing membrane GRP78
    Florence Delie
    Patrick Petignat
    Marie Cohen
    [J]. Targeted Oncology, 2013, 8 : 225 - 230
  • [38] Protein C Nagoya, an elongated mutant of protein C, is retained within the endoplasmic reticulum and is associated with GRP78 and GRP94
    Katsumi, A
    Senda, T
    Yamashita, Y
    Yamazaki, T
    Hamaguchi, R
    Kojima, T
    Kobayashi, S
    Saito, H
    [J]. BLOOD, 1996, 87 (10) : 4164 - 4175
  • [39] GRP78和GRP94表达与结直肠癌的侵袭及预后相关
    关心
    张楼乾
    曲渊
    周建农
    [J]. 中华普通外科杂志, 2011, (12)
  • [40] Ultrasensitive Detection of GRP78 in Exosomes and Observation of Migration and Proliferation of Cancer Cells by Application of GRP78-Containing Exosomes
    Tsurusawa, Naoko
    Iha, Kanako
    Sato, Akane
    Tsai, Hsin-Yi
    Sonoda, Hikaru
    Watabe, Satoshi
    Yoshimura, Teruki
    Wu, Deng-Chyang
    Lin, Ming-Wei
    Ito, Etsuro
    [J]. CANCERS, 2022, 14 (16)