Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Via Albertoni-15, 40138 Bologna, Italy.
Oncology Unit, Macerata Hospital, 62100 Macerata, Italy.
Int J Mol Sci. 2021 Dec 16;22(24):13519. doi: 10.3390/ijms222413519.
Prostate cancer is still one of the main causes of cancer-related death in the male population, regardless of the advancements in the treatment scenario. The genetic knowledge on prostate cancer is widely increasing, allowing researchers to identify novel promising molecular targets and treatment approaches. Genomic profiling has evidenced that DNA damage repair genes' alterations are quite frequent in metastatic, castration resistant prostate cancer and specific therapies can interfere with this pathway, showing promising activity in this setting. Microsatellite instability is gaining attention as it seems to represent a predictive factor of the response to immunotherapy. Furthermore, the PTEN-PI3K-AKT pathway is another possible treatment target being investigated. In this review, we explore the current knowledge on these frequent genomic alterations of metastatic prostate cancer, their possible therapeutic repercussions and the promising future treatments under evaluation.
前列腺癌仍然是男性人群中癌症相关死亡的主要原因之一,尽管在治疗方案方面取得了进展。前列腺癌的遗传知识正在广泛增加,这使得研究人员能够识别新的有前途的分子靶点和治疗方法。基因组分析表明,转移性去势抵抗性前列腺癌中 DNA 损伤修复基因的改变相当频繁,特定的治疗方法可以干扰该途径,在这种情况下显示出有希望的活性。微卫星不稳定性越来越受到关注,因为它似乎是对免疫治疗反应的预测因素。此外,PTEN-PI3K-AKT 途径也是另一个正在研究的可能的治疗靶点。在这篇综述中,我们探讨了转移性前列腺癌中这些常见基因组改变的最新知识,以及它们可能的治疗影响和正在评估的有前途的未来治疗方法。