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首页> 外文期刊>American Journal of Clinical and Experimental Urology >Proinflammatory cytokine interleukin-6 in prostate carcinogenesis
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Proinflammatory cytokine interleukin-6 in prostate carcinogenesis

机译:促炎细胞因子白介素6在前列腺癌发生中的作用

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Interleukin-6 (IL-6) is a multifunctional pro-inflammatory cytokine which is expressed in clinical specimens obtained from patients with prostate cancer and in multiple cell lines. IL-6 expression is regulated in prostate cancer by several oncogenes and tumor suppressors. IL-6 activates in prostate cancer pathways of Janus kinases/signal transducers and activators of transcription (STAT), mitogen-activated protein kinases, and phosphatidylinositol 3-kinase. In several tumor models, proliferative and anti-apoptotic effects were described, although androgen-sensitive prostate cancer cells LNCaP are inhibited by IL-6. IL-6 is also involved in regulation of neuroendocrine differentiation and angiogenesis in prostate cancer. IL-6 activation of the androgen receptor is important for tumor growth and differentiation. IL-6 activation of STAT3 is crucial for maintenance of the tumor progenitor cells phenotype. Suppressors of cytokine signaling inhibit permanent activation of STAT3, however they may have also IL-6-independent effects. Experimental therapies with aim to inhibit IL-6 signaling in prostate cancer were developed with the monoclonal antibody CNTO328. Although progression towards castration resistance was delayed by CNTO328 in a xenograft model, clinical monotherapies in patients with castration therapy-resistant disease with the antibody did not yield a satisfactory response.
机译:白介素6(IL-6)是一种多功能促炎性细胞因子,在前列腺癌患者的临床标本和多种细胞系中表达。 IL-6表达在前列腺癌中受几种癌基因和肿瘤抑制因子的调控。 IL-6在Janus激酶/信号转导子和转录激活子(STAT),有丝分裂原激活的蛋白激酶和磷脂酰肌醇3激酶的前列腺癌途径中激活。在几种肿瘤模型中,尽管雄激素敏感的前列腺癌细胞LNCaP被IL-6抑制,但仍具有增殖和抗凋亡作用。 IL-6也参与前列腺癌的神经内分泌分化和血管生成的调控。雄激素受体的IL-6激活对于肿瘤的生长和分化很重要。 STAT3的IL-6激活对于维持肿瘤祖细胞表型至关重要。细胞因子信号传导抑制剂可抑制STAT3的永久激活,但它们也可能具有IL-6依赖性。用单克隆抗体CNTO328开发了旨在抑制前列腺癌中IL-6信号转导的实验疗法。尽管在异种移植模型中,CNTO328延缓了去势抵抗的进展,但是对于具有抗体的去势疗法耐药性疾病的患者,临床单一疗法并未产生令人满意的应答。

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