TRPM4 channel and cancer

被引:45
作者
Gao, Yahui [1 ]
Liao, Ping [1 ,2 ,3 ]
机构
[1] Natl Neurosci Inst, Calcium Signalling Lab, 11 Jalan Tan Tock Seng, Singapore 308433, Singapore
[2] Duke NUS Med Sch, Singapore, Singapore
[3] Singapore Inst Technol, Hlth & Social Sci, Singapore, Singapore
基金
英国医学研究理事会;
关键词
Migration; Invasion; Proliferation; Ion channels; Calcium; Cancer; PROSTATE-CANCER; MICROARRAY ANALYSIS; CALCIUM-CHANNELS; GENE-EXPRESSION; CELL-MIGRATION; METASTASIS; INVASION; ACTIVATION; TRANSITION; SURVIVAL;
D O I
10.1016/j.canlet.2019.04.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The TRPM4 channel has been extensively studied in cerebral diseases such as stroke, head injury and multiple sclerosis. In the heart, gain-of-function mutations of TRPM4 are a cause of familial cardiac block. Recently, evidence has emerged to support the role of TRPM4 in certain types of cancer, such as prostate cancer and large B cell lymphoma. The expression of TRPM4 could mediate certain behaviors of cancer cells such as migration and invasion. However, the mechanisms are largely unknown. As a nonselective monovalent cation channel, TRPM4 upregulation and activation enhance sodium entry, which leads to depolarization of the membrane potential. The membrane potential is critical in regulating calcium influx, and a disturbed calcium homeostasis is always associated with cancer cell behaviors. Research on TRPM4 channels in cancer is at a very early stage. In this review, we summarize the expression of TRPM4 in various cancers as well as our current understanding of TRPM4 in cancer. The potential mechanisms of the TRPM4 channel in regulating calcium homeostasis in cancer cells are further discussed in detail. Targeting the TRPM4 channel can be a novel way of managing cancer metastasis via disrupting calcium signaling pathways.
引用
收藏
页码:66 / 69
页数:4
相关论文
共 42 条
[1]   TRPM4 Enhances Cell Proliferation Through Up-Regulation of the β-Catenin Signaling Pathway [J].
Armisen, Ricardo ;
Marcelain, Katherine ;
Simon, Felipe ;
Tapia, Julio C. ;
Toro, Jessica ;
Quest, Andrew F. G. ;
Stutzin, Andres .
JOURNAL OF CELLULAR PHYSIOLOGY, 2011, 226 (01) :103-109
[2]   Molecular features of the transition from prostatic intraepithelial neoplasia (PIN) to prostate cancer: Genome-wide gene-expression profiles of prostate cancers and PINs [J].
Ashida, S ;
Nakagawa, H ;
Katagiri, T ;
Furihata, M ;
Iiizumi, M ;
Anazawa, Y ;
Tsunoda, T ;
Takata, R ;
Kasahara, K ;
Miki, T ;
Fujioka, T ;
Shuin, T ;
Nakamura, Y .
CANCER RESEARCH, 2004, 64 (17) :5963-5972
[3]   The calcium-activated nonselective cation channel TRPM4 is essential for the migration but not the maturation of dendritic cells [J].
Barbet, Gaetan ;
Demion, Marie ;
Moura, Ivan C. ;
Serafini, Nicolas ;
Leger, Thibaut ;
Vrtovsnik, Francois ;
Monteiro, Renato C. ;
Guinamard, Romain ;
Kinet, Jean-Pierre ;
Launay, Pierre .
NATURE IMMUNOLOGY, 2008, 9 (10) :1148-1156
[4]   TRPM4 protein expression in prostate cancer: a novel tissue biomarker associated with risk of biochemical recurrence following radical prostatectomy [J].
Berg, Kasper Drimer ;
Soldini, Davide ;
Jung, Maria ;
Dietrich, Dimo ;
Stephan, Carsten ;
Jung, Klaus ;
Dietel, Manfred ;
Vainer, Ben ;
Kristiansen, Glen .
VIRCHOWS ARCHIV, 2016, 468 (03) :345-355
[5]   Evidence for specific TRPM8 expression in human prostate secretory epithelial cells:: functional androgen receptor requirement [J].
Bidaux, G ;
Roudbaraki, M ;
Merle, C ;
Crépin, A ;
Delcourt, P ;
Slomianny, C ;
Thebault, S ;
Bonnal, JL ;
Benahmed, M ;
Cabon, F ;
Mauroy, B ;
Prevarskaya, N .
ENDOCRINE-RELATED CANCER, 2005, 12 (02) :367-382
[6]   Disentangling the role of TRPM4 in hippocampus-dependent plasticity and learning: an electrophysiological, behavioral and FMRI approach [J].
Bovet-Carmona, Marta ;
Menigoz, Aurelie ;
Pinto, Silvia ;
Tambuyzer, Tim ;
Krautwald, Karla ;
Voets, Thomas ;
Aerts, Jean-Marie ;
Angenstein, Frank ;
Vennekens, Rudi ;
Balschun, Detlef .
BRAIN STRUCTURE & FUNCTION, 2018, 223 (08) :3557-3576
[7]   TRPM4 Is a Novel Component of the Adhesome Required for Focal Adhesion Disassembly, Migration and Contractility [J].
Caceres, Monica ;
Ortiz, Liliana ;
Recabarren, Tatiana ;
Romero, Anibal ;
Colombo, Alicia ;
Leiva-Salcedo, Elias ;
Varela, Diego ;
Rivas, Jose ;
Silva, Ian ;
Morales, Diego ;
Campusano, Camilo ;
Almarza, Oscar ;
Simon, Felipe ;
Toledo, Hector ;
Park, Kang-Sik ;
Trimmer, James S. ;
Cerda, Oscar .
PLOS ONE, 2015, 10 (06)
[8]   Potential role of melastatin-related transient receptor potential cation channel subfamily M gene expression in the pathogenesis of urinary bladder cancer [J].
Ceylan, Gulay Gulec ;
Onalan, Ebru Etem ;
Kuloglu, Tuncay ;
Aydog, Gulten ;
Keles, Ibrahim ;
Tonyali, Senol ;
Ceylan, Cavit .
ONCOLOGY LETTERS, 2016, 12 (06) :5235-5239
[9]   Non-Invasive Multimodality Imaging Directly Shows TRPM4 Inhibition Ameliorates Stroke Reperfusion Injury [J].
Chen, Bo ;
Ng, Gandi ;
Gao, Yahui ;
Low, See Wee ;
Sandanaraj, Edwin ;
Ramasamy, Boominathan ;
Sekar, Sakthivel ;
Bhakoo, Kishore ;
Soong, Tuck Wah ;
Nilius, Bernd ;
Tang, Carol ;
Robins, Edward G. ;
Goggi, Julian ;
Liao, Ping .
TRANSLATIONAL STROKE RESEARCH, 2019, 10 (01) :91-103
[10]   Transient receptor potential (TRP) channels, promising potential diagnostic and therapeutic tools for cancer [J].
Chen, Jianpeng ;
Luan, Yi ;
Yu, Ruofei ;
Zhang, Zheng ;
Zhang, Jinbiao ;
Wang, Weibo .
BIOSCIENCE TRENDS, 2014, 8 (01) :1-10