Downregulation of LRRC8A protects human ovarian and alveolar carcinoma cells against Cisplatin-induced expression of p53, MDM2, p21Waf1/Cip1, and Caspase-9/-3 activation

被引:50
|
作者
Sorensen, Belinda Halling [1 ]
Nielsen, Dorthe [1 ]
Thorsteinsdottir, Unnur Arna [1 ]
Hoffmann, Else Kay [1 ]
Lambert, Ian Henry [1 ]
机构
[1] Univ Copenhagen, Dept Biol, Sect Cell Biol & Physiol, August Krogh Bldg, Copenhagen, Denmark
来源
关键词
platinum drugs; multidrug resistance; organic anion channels; transcription factors; taurine; apoptosis; SENSITIVE CHLORIDE CHANNELS; LUNG ADENOCARCINOMA CELLS; CANCER-CELLS; ANION CHANNEL; TUMOR-CELLS; MOLECULAR-IDENTIFICATION; MULTIDRUG-RESISTANCE; ESSENTIAL COMPONENT; VOLUME; MECHANISMS;
D O I
10.1152/ajpcell.00256.2015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The leucine-rich repeat containing 8A (LRRC8A) protein is an essential component of the volume-sensitive organic anion channel (VSOAC), and using pharmacological anion channel inhibitors (NS3728, DIDS) and LRRC8A siRNA we have investigated its role in development of Cisplatin resistance in human ovarian (A2780) and alveolar (A549) carcinoma cells. In Cisplatin-sensitive cells Cisplatin treatment increases p53-protein level as well as downstream signaling, e. g., expression of p21(Waf1/Cip1), Bax, Noxa, MDM2, and activation of Caspase-9/-3. In contrast, Cisplatin-resistant cells do not enter apoptosis, i.e., their p53 and downstream signaling are reduced and caspase activity unaltered following Cisplatin exposure. Reduced LRRC8A expression and VSOAC activity are previously shown to correlate with Cisplatin resistance, and here we demonstrate that pharmacological inhibition and transient knockdown of LRRC8A reduce the protein level of p53, MDM2, and p21(Waf1/Cip1) as well as Caspase-9/-3 activation in Cisplatin-sensitive cells. Cisplatin resistance is accompanied by reduction in total LRRC8A expression (A2780) or LRRC8A expression in the plasma membrane (A549). Activation of Caspase-3 dependent apoptosis by TNF alpha-exposure or hyperosmotic cell shrinkage is almost unaffected by pharmacological anion channel inhibition. Our data indicate 1) that expression/activity of LRRC8A is essential for Cisplatin-induced increase in p53 protein level and its downstream signaling, i.e., Caspase-9/-3 activation, expression of p21(Waf1/Cip1) and MDM2; and 2) that downregulation of LRRC8A-dependent osmolyte transporters contributes to acquirement of Cisplatin resistance in ovarian and lung carcinoma cells. Activation of LRRC8A-containing channels is upstream to apoptotic volume decrease as hypertonic cell shrinkage induces apoptosis independent of the presence of LRRC8A.
引用
收藏
页码:C857 / C873
页数:17
相关论文
共 50 条
  • [21] Analysis of p53 Mutations and the Expression of p53 and p21WAF1/CIP1 Protein in 15 Cases of Sebaceous Carcinoma of the Eyelid
    Kiyosaki, Kunihiro
    Nakada, Chisato
    Hijiya, Naoki
    Tsukamoto, Yoshiyuki
    Matsuura, Keiko
    Nakatsuka, Kazuo
    Daa, Tsutomu
    Yokoyama, Shigeo
    Imaizumi, Masamoto
    Moriyama, Masatsugu
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2010, 51 (01) : 7 - 11
  • [22] p21WAF1/CIP1 expression in colorectal carcinoma correlates with advanced disease stage and p53 mutations
    Viale, G
    Pellegrini, C
    Mazzarol, G
    Maisonneuve, P
    Silverman, ML
    Bosari, S
    JOURNAL OF PATHOLOGY, 1999, 187 (03): : 302 - 307
  • [23] P21WAF1/Cip1 gene expression in primary human hepatocellular carcinoma and its relationship with P53 gene mutation
    Sun Baohua
    Wu Zhongbi
    Ruan Youbing
    Yang Mulan
    Liu Bing
    Journal of Tongji Medical University, 1999, 19 (1) : 1 - 5
  • [25] p21WAF1/CIP1 promotes p53 protein degradation by facilitating p53-Wip1 and p53-Mdm2 interaction
    Lee, Jihyun
    Kim, Jongdoo
    Kim, Eun Mi
    Kim, Ukjin
    Kang, A-Ram
    Park, Jong Kuk
    Um, Hong-Duck
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2021, 543 : 23 - 28
  • [26] Immunoreactivity of p53, Mdm2, p21WAF1/CIP1, Bcl-2, and Bax in soft tissue sarcomas -: Correlation with histologic grade
    Sabah, Muna
    Cummins, Robert
    Leader, Mary
    Kay, Elaine
    APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY, 2007, 15 (01) : 64 - 69
  • [27] Immunoreactivity of p53, Mdm2, p21WAF1/CIP1 Bcl-2 and Bax in soft tissue sarcomas:: Correlation with histologic grade
    Sabah, M.
    Cummins, R.
    Leader, M.
    Kay, E.
    JOURNAL OF PATHOLOGY, 2006, 210 : 23 - 23
  • [28] Enhancement of drug-induced apoptosis by anti sense oligodeoxynucleotides targeted against Mdm2 and p21WAF1/CIP1
    Sato, N
    Mizumoto, K
    Maehara, N
    Kusumoto, M
    Nishio, S
    Urashima, T
    Ogawa, T
    Tanaka, M
    ANTICANCER RESEARCH, 2000, 20 (2A) : 837 - 842
  • [29] Expression of p53 and p21waf1/cip1 in gastric carcinoma:: lack of inter-relationship or correlation with prognosis
    Kaye, PV
    Radebold, K
    Isaacs, S
    Dent, DM
    EUROPEAN JOURNAL OF SURGICAL ONCOLOGY, 2000, 26 (01): : 39 - 43
  • [30] p53, WAF1/CIP1 and mdm2 expression in skin lesions associated with human papillomavirus and human immunodeficiency virus
    Arany, I
    Yen, A
    Tyring, SK
    ANTICANCER RESEARCH, 1997, 17 (2B) : 1281 - 1285