Pencik Jan, Wiebringhaus Robert, Susani Martin, Culig Zoran, Kenner Lukas
Ludwig Boltzmann Institute for Cancer Research, Medical University of Vienna, Austria; Clinical Institute of Pathology, Medical University of Vienna, Austria.
Clinical Institute of Pathology, Medical University of Vienna, Austria.
Swiss Med Wkly. 2015 Dec 21;145:w14215. doi: 10.4414/smw.2015.14215. eCollection 2015.
Prostate cancer is one of the most prevalent forms of cancer in men worldwide. It remains a clinical challenge to identify lethal metastatic prostate cancers, which escape standard therapeutic intervention. Aberrant interleukin-6 (IL-6) / signal transducer and activator of transcription-3 (STAT3) signalling and loss of p53 occur during prostate cancer progression to metastatic disease. The abnormality of the IL-6/STAT3/p53 axis is frequently accompanied by other genetic alterations; however, its potential role as an important mediator of oncogenic reprogramming, invasion and metastatic transformation remains unknown. The failure of anti-IL-6 treatments is still unexplained and may be due to an incomplete understanding of the mechanism of the in vivo role of IL-6/STAT3 in prostate cancer. The identification of the alternative reading frame protein (ARF) / murine double minute protein (MDM2) / p53 tumour suppressor pathway potentially involving the IL-6/STAT3 axis as a restricting factor in prostate cancer deficient in the tumour suppressor phosphatase and tensin homologue (PTEN) opened new avenues to currently available therapies. This review summarises the current knowledge on the role of crucial pathways driving prostate cancer progression as well as metastatic disease and discusses the potential use of novel specific target molecules and how it can be exploited to avoid overtreatment and increase quality of life.
前列腺癌是全球男性中最常见的癌症形式之一。识别致命的转移性前列腺癌仍然是一项临床挑战,这类癌症会逃避标准的治疗干预。在前列腺癌发展为转移性疾病的过程中,会出现异常的白细胞介素-6(IL-6)/信号转导和转录激活因子3(STAT3)信号传导以及p53缺失。IL-6/STAT3/p53轴的异常常常伴随着其他基因改变;然而,其作为致癌重编程、侵袭和转移转化重要介质的潜在作用仍不清楚。抗IL-6治疗的失败原因仍未得到解释,可能是由于对IL-6/STAT3在前列腺癌体内作用机制的理解不完整。识别出替代阅读框蛋白(ARF)/鼠双微体蛋白(MDM2)/p53肿瘤抑制途径可能涉及IL-6/STAT3轴,作为肿瘤抑制因子磷酸酶和张力蛋白同源物(PTEN)缺陷型前列腺癌的限制因素,为当前可用的治疗方法开辟了新途径。本综述总结了目前关于驱动前列腺癌进展以及转移性疾病的关键途径作用的知识,并讨论了新型特异性靶分子的潜在用途以及如何利用它来避免过度治疗并提高生活质量。