Sun Ke, Xu Dechao, Mei Changlin
Department of Nephrology, Kidney Institute, Changzheng Hospital, Second Military Medical University, No. 415 Fengyang Road, Shanghai, 200003, China.
Int Urol Nephrol. 2019 Jan;51(1):93-100. doi: 10.1007/s11255-018-1951-5. Epub 2018 Aug 14.
Autosomal dominant polycystic kidney disease (ADPKD) is considered as a tumor-like disease because there are many biological similarities between ADPKD and cancer. However, the commonalities between them are provocative, particularly under the conditions of recent clinical studies. In this paper, we review clinical studies about the association between cancer and ADPKD, and compare the biological characteristics between them, with focusing on cell proliferation, differentiation, migration, apoptosis, and polarity. With detailed literature reviewing, we believe that ADPKD patients have a higher risk of tumorigenesis and thus highly recommend being aware of tumorigenesis during follow-up in patients with ADPKD.
常染色体显性多囊肾病(ADPKD)被认为是一种肿瘤样疾病,因为ADPKD与癌症之间存在许多生物学相似性。然而,它们之间的共性具有启发性,特别是在近期临床研究的背景下。在本文中,我们回顾了关于癌症与ADPKD关联的临床研究,并比较了它们之间的生物学特性,重点关注细胞增殖、分化、迁移、凋亡和极性。通过详细的文献综述,我们认为ADPKD患者具有更高的肿瘤发生风险,因此强烈建议在ADPKD患者的随访过程中关注肿瘤发生情况。