Department of Urology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Division of Diagnostic Pathology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Int J Mol Sci. 2022 May 5;23(9):5154. doi: 10.3390/ijms23095154.
To evaluate biological characteristics and transitions of upper tract urothelial carcinoma (UTUC) through metachronous bladder tumors after radical nephroureterectomy (RNU), we conducted immunohistochemical (IHC) staining of tumor specimens of UTUC tumor origin, non-muscle-invasive bladder cancer (NMIBC) and MIBC progressed after intravesical recurrence (IVR), and bladder primary MIBC. Fibroblast growth factor receptor 3 (FGFR3), p53, cytokeratin 5/6 (CK5/6), and CK20 were stained to examine expression rates. After expression assessment with heatmap clustering, the overexpression of four biomarkers from UTUC origin to metachronous MIBC progression was analyzed with clinicopathological variables. We found that high CK20 and low CK5/6 expression were both observed in UTUC tumor origin and subsequent NMIBC after RNU. By investigating molecular expression in the IVR specimen, we observed that low pT stage bladder recurrence occupied the majority of CK20 high CK5/6 low expression, but would change to CK20 low CK5/6 high expression as it progressed to MIBC. UTUC metachronous MIBC has different characteristics compared with bladder primary MIBC, which comprises favorable biological features such as high FGFR3 expression, and follows favorable prognosis compared to those without FGFR3 expression. The present study demonstrated that the biological characteristics of UTUC tumor origin shifts from luminal to basal-like features with progression to MIBC, but FGFR3 expression taken over from UTUC origin may comprise a favorable entity compared to primary MIBC.
为了评估根治性肾输尿管切除术(RNU)后顺行膀胱癌发生的上尿路上皮癌(UTUC)的生物学特征和转移,我们对 UTUC 肿瘤起源、非肌肉浸润性膀胱癌(NMIBC)和肌层浸润性膀胱癌(MIBC)进行了免疫组织化学(IHC)染色肿瘤标本经膀胱内复发(IVR)后复发和膀胱原发性 MIBC。检测了成纤维细胞生长因子受体 3(FGFR3)、p53、细胞角蛋白 5/6(CK5/6)和 CK20 的表达率。在用热图聚类进行表达评估后,分析了从 UTUC 起源到顺行 MIBC 进展的四个生物标志物的过度表达与临床病理变量的关系。我们发现 UTUC 肿瘤起源和 RNU 后随后发生的 NMIBC 中均观察到 CK20 高和 CK5/6 低表达。通过研究 IVR 标本中的分子表达,我们观察到低 pT 期膀胱复发主要占据 CK20 高 CK5/6 低表达,但随着进展为 MIBC,它会变为 CK20 低 CK5/6 高表达。与原发性膀胱 MIBC 相比,UTUC 顺行 MIBC 具有不同的特征,包括 FGFR3 表达较高的有利生物学特征,并且与 FGFR3 无表达相比,预后较好。本研究表明,UTUC 肿瘤起源的生物学特征从腔型向基底样特征转变,进展为 MIBC,但 FGFR3 表达可能取代 UTUC 起源,构成比原发性 MIBC 更有利的实体。