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Inflammation and prostate cancer: the role of interleukin 6 ( IL ‐6)
Author(s) -
Nguyen Daniel P.,
Li Jinyi,
Tewari Ashutosh K.
Publication year - 2014
Publication title -
bju international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.773
H-Index - 148
eISSN - 1464-410X
pISSN - 1464-4096
DOI - 10.1111/bju.12452
Subject(s) - prostate cancer , cancer research , janus kinase , stat protein , mapk/erk pathway , stat3 , signal transduction , biology , jak stat signaling pathway , medicine , cancer , tyrosine kinase , immunology , microbiology and biotechnology
Environmental and genetic aspects are reflected in the development of prostate cancer. In this context, there is growing evidence that chronic inflammation is involved in the regulation of cellular events in prostate carcinogenesis, including disruption of the immune response and regulation of the tumour microenvironment. One of the best surrogates of chronic inflammation in prostate cancer is interleukin 6 ( IL ‐6). Serum IL ‐6 levels are elevated in patients with untreated metastatic or castration‐resistant prostate cancer ( CRPC ) and correlate negatively with tumour survival and response to chemotherapy. Via multiple signal pathways including the J anus tyrosine family kinase ( JAK )‐signal transducer and activator of transcription ( STAT ) pathway, the extracellular signal‐regulated kinase 1 and 2 ( ERK 1/2)‐mitogen activated protein kinase ( MAPK ) pathway, and the phosphoinositide 3‐kinase ( PI 3‐ K ) pathway, IL ‐6 is able to promote prostate cancer cell proliferation and inhibit apoptosis in vitro and in vivo . IL ‐6 is associated with aggressive prostate cancer phenotype and may be involved in the metastatic process through regulation of epithelial–mesenchymal transition ( EMT ) and homing of cancer cells to the bone. A substantial body of evidence suggests that IL ‐6 plays a major role in the transition from hormone‐dependent to CRPC , most notably through accessory activation of the androgen receptor. Collectively, these data have stimulated the development of agents targeting IL ‐6 signalling pathways. A chimeric anti‐ IL ‐6 monoclonal antibody has been tested in clinical trials, with mixed results.