Inoue Chihiro, Saito Ryoko, Nakanishi Wataru, Kumata Hiroyuki, Eba Shunsuke, Fujishima Fumiyoshi, Watanabe Mika, Sasano Hironobu
Department of Anatomic Pathology, Tohoku University Graduate School of Medicine.
Department of Surgery, Tohoku University Graduate School of Medicine.
Tohoku J Exp Med. 2019 Feb;247(2):119-127. doi: 10.1620/tjem.247.119.
Epithelioid angiomyolipoma (EAML) has been known as a potentially malignant tumor which occasionally recur and/or metastasize to other organs, and clinically and pathologically recognized as distinct entity. However, the mechanisms of recurrence and/or metastasis (recurrence/metastasis) has still remained unknown. Here, we report two cases of renal EAML associated with recurrence/metastasis, and three cases of EAML in kidney or liver without recurrence/metastasis. According to the previous histological predictive models of EAML, the primary tumor was classified as low risk group in one of the cases with recurrence/metastasis in spite of its malignant behavior. Therefore, we considered that further investigation about the mechanisms of recurrence/metastasis in EAML is required for a malignancy prediction. We focused on some cell-cycle modulators, including mouse double minute 2 homolog (MDM2), which is ubiquitin ligase well-known to promote malignant behaviors by p53 ubiquitination and degradation, and also other cellular processes including genomic instability and epithelial-mesenchymal transition in p53-independent manners in various human malignancies. Immunohistochemical evaluation revealed that MDM2 protein expression increased stepwise throughout every steps of metastasis/recurrence in both cases, although it was negative in primary tumors. In conclusion, this is the first study demonstrating that MDM2 could play an important role in the molecular mechanisms of recurrence/metastasis of EAML. Further analyses focusing on MDM2 pathway could contribute to the identification of novel prognostic factors and/or therapeutic targets in EAML patients.
上皮样血管平滑肌脂肪瘤(EAML)被认为是一种具有潜在恶性的肿瘤,偶尔会复发和/或转移至其他器官,在临床和病理上被视为一种独特的实体。然而,其复发和/或转移的机制仍不清楚。在此,我们报告2例伴有复发/转移的肾EAML病例,以及3例无复发/转移的肾或肝EAML病例。根据先前的EAML组织学预测模型,尽管其中1例伴有复发/转移的病例具有恶性行为,但其原发肿瘤仍被归类为低风险组。因此,我们认为需要进一步研究EAML复发/转移的机制以进行恶性预测。我们关注了一些细胞周期调节因子,包括小鼠双微体2同源物(MDM2),它是一种泛素连接酶,通过使p53泛素化和降解来促进恶性行为,并且在各种人类恶性肿瘤中还以不依赖p53的方式参与包括基因组不稳定和上皮-间质转化在内的其他细胞过程。免疫组织化学评估显示,在这2例病例中,尽管原发肿瘤中MDM2蛋白表达为阴性,但在转移/复发的各个阶段中其表达均呈逐步增加。总之,这是第一项表明MDM2可能在EAML复发/转移的分子机制中发挥重要作用的研究。进一步针对MDM2通路的分析可能有助于识别EAML患者新的预后因素和/或治疗靶点。