Inflammation and NF-κB Signaling in Prostate Cancer: Mechanisms and Clinical Implications

被引:87
作者
Staal, Jens [1 ,2 ]
Beyaert, Rudi [1 ,2 ]
机构
[1] VIB, Unit Mol Signal Transduct Inflammat, VIB UGent Ctr Inflammat Res, B-9052 Ghent, Belgium
[2] Univ Ghent, Dept Biomed Mol Biol, B-9000 Ghent, Belgium
关键词
prostate; cancer; androgen; castration; inflammation; NF-kappa B; cytokines; protein kinase C; signaling; clinical; KINASE-C-EPSILON; ANDROGEN-DEPRIVATION THERAPY; PROTEIN-COUPLED RECEPTOR; TRANSCRIPTION FACTOR; TUMOR-GROWTH; TNF-ALPHA; REGULATING INFLAMMATION; INHIBITOR SOTRASTAURIN; CELL-PROLIFERATION; FEMALE PROSTATE;
D O I
10.3390/cells7090122
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Prostate cancer is a highly prevalent form of cancer that is usually slow-developing and benign. Due to its high prevalence, it is, however, still the second most common cause of death by cancer in men in the West. The higher prevalence of prostate cancer in the West might be due to elevated inflammation from metabolic syndrome or associated comorbidities. NF-kappa B activation and many other signals associated with inflammation are known to contribute to prostate cancer malignancy. Inflammatory signals have also been associated with the development of castration resistance and resistance against other androgen depletion strategies, which is a major therapeutic challenge. Here, we review the role of inflammation and its link with androgen signaling in prostate cancer. We further describe the role of NF-kappa in prostate cancer cell survival and proliferation, major NF-kappa B signaling pathways in prostate cancer, and the crosstalk between NF-kappa B and androgen receptor signaling. Several NF-kappa B-induced risk factors in prostate cancer and their potential for therapeutic targeting in the clinic are described. A better understanding of the inflammatory mechanisms that control the development of prostate cancer and resistance to androgen-deprivation therapy will eventually lead to novel treatment options for patients.
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页数:20
相关论文
共 194 条
[1]   Limiting inflammation-the negative regulation of NF-κB and the NLRP3 inflammasome [J].
Afonina, Inna S. ;
Zhong, Zhenyu ;
Karin, Michael ;
Beyaert, Rudi .
NATURE IMMUNOLOGY, 2017, 18 (08) :861-869
[2]   Expression of Id proteins is regulated by the Bcl-3 proto-oncogene in prostate cancer [J].
Ahlqvist, K. ;
Saamarthy, K. ;
Khaja, A. S. Syed ;
Bjartell, A. ;
Massoumi, R. .
ONCOGENE, 2013, 32 (12) :1601-1608
[3]   Oncogenic Role of Tumor Viruses in Humans [J].
Akram, Nimrah ;
Imran, Muhammad ;
Noreen, Mamoona ;
Ahmed, Fayyaz ;
Atif, Muhammad ;
Fatima, Zareen ;
Waqar, Ahmed Bilal .
VIRAL IMMUNOLOGY, 2017, 30 (01) :20-27
[4]   Thrombotic characteristics of extracellular vesicles derived from prostate cancer cells [J].
Al Saleh, Hassan A. ;
Haas-Neill, Sandor ;
Al-Hashimi, Ali ;
Kapoor, Anil ;
Shayegan, Bobby ;
Austin, Richard C. ;
Al-Nedawi, Khalid .
PROSTATE, 2018, 78 (13) :953-961
[5]   IκBζ is a regulator of the senescence-associated secretory phenotype in DNA damage- and oncogene-induced senescence [J].
Alexander, Eva ;
Hildebrand, Dominic G. ;
Kriebs, Anna ;
Obermayer, Kerstin ;
Manz, Marianne ;
Rothfuss, Oliver ;
Schulze-Osthoff, Klaus ;
Essmann, Frank .
JOURNAL OF CELL SCIENCE, 2013, 126 (16) :3738-3745
[6]   B-cell-derived lymphotoxin promotes castration-resistant prostate cancer [J].
Ammirante, Massimo ;
Luo, Jun-Li ;
Grivennikov, Sergei ;
Nedospasov, Sergei ;
Karin, Michael .
NATURE, 2010, 464 (7286) :302-U187
[7]  
[Anonymous], JAMA
[8]   Interleukin-8 is a molecular determinant of androgen independence and progression in prostate cancer [J].
Araki, Shinako ;
Omori, Yohei ;
Lyn, Dominic ;
Singh, Rajendra K. ;
Meinbach, David M. ;
Sandman, Yekutiel ;
Lokeshwar, Vinata B. ;
Lokeshwar, Bal L. .
CANCER RESEARCH, 2007, 67 (14) :6854-6862
[9]  
Aultman B., 2014, TSQ: Transgender Studies Quarterly, V1, P61, DOI DOI 10.1215/23289252-2399614
[10]   NF-B and androgen receptor variant 7 induce expression of SRD5A isoforms and confer 5ARI resistance [J].
Austin, David C. ;
Strand, Douglas W. ;
Love, Harold L. ;
Franco, Omar E. ;
Grabowska, Magdalena M. ;
Miller, Nicole L. ;
Hameed, Omar ;
Clark, Peter E. ;
Matusik, Robert J. ;
Jin, Ren J. ;
Hayward, Simon W. .
PROSTATE, 2016, 76 (11) :1004-1018