Topographic modification of the extracellular matrix precedes the onset of bladder cancer

Q1 Medicine Matrix Biology Plus Pub Date : 2024-06-02 DOI:10.1016/j.mbplus.2024.100154
Chiara Venegoni , Filippo Pederzoli , Irene Locatelli , Elisa Alchera , Laura Martinez-Vidal , Alessia Di Coste , Marco Bandini , Andrea Necchi , Francesco Montorsi , Andrea Salonia , Marco Moschini , Jithin Jose , Federico Scarfò , Roberta Lucianò , Massimo Alfano
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Abstract

Background

Non-muscle invasive bladder cancer (NMIBC) patients are affected by a high risk of recurrence. The topography of collagen fibers represents a hallmark of the neoplastic extracellular microenvironment.

Objective

Assess the topographic change associated with different stages of bladder cancer (from neoplastic lesions to bona fide tumor) and whether those changes favour the development of NMIBC.

Design, Setting, and Participants

Seventy-one clinical samples of urothelial carcinoma at different stages were used. Topographic changes preceding tumor onset and progression were evaluated in the rat bladder cancer model induced by nitrosamine (BBN), a bladder-specific carcinogen. The preclinical model of actinic cystitis was also used in combination with BBN. Validated hematoxylin-eosin sections were used to assess the topography of collagen fibrils associated with pre-tumoral steps, NMIBC, and MIBC.

Findings

Linearization of collagen fibers was higher in Cis and Ta vs. dysplastic urothelium, further increased in T1 and greatest in T2 tumors. In the BBN preclinical model, an increase in the linearization of collagen fibers was established since the beginning of inflammation, such as the onset of atypia of a non-univocal nature and dysplasia, and further increased in the presence of the tumor. Linearization of collagen fibers in the model of actinic cystitis was associated with earlier onset of BBN-induced tumor.

Conclusions

The topographic modification of the extracellular microenvironment occurs during the inflammatory processes preceding and favoring the onset of bladder cancer. The topographic reconfiguration of the stroma could represent a marker for identifying and treating the non-neoplastic tissue susceptible to tumor recurrence.

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细胞外基质的拓扑结构改变先于膀胱癌发病
背景非肌层浸润性膀胱癌(NMIBC)患者的复发风险很高。目的评估与膀胱癌不同阶段(从肿瘤病变到真正的肿瘤)相关的地形变化,以及这些变化是否有利于非肌层浸润性膀胱癌的发展。在亚硝胺(BBN)(一种膀胱特异性致癌物质)诱导的大鼠膀胱癌模型中,对肿瘤发生和发展之前的地形变化进行了评估。此外,还将光化性膀胱炎的临床前模型与 BBN 结合使用。通过验证苏木精-伊红切片来评估与瘤前步骤、NMIBC 和 MIBC 相关的胶原纤维的形貌。研究结果Cis 和 Ta 与发育不良的尿路上皮相比,胶原纤维的线性化程度更高,在 T1 肿瘤中进一步增加,而在 T2 肿瘤中最大。在 BBN 临床前模型中,胶原纤维线性化的增加自炎症开始时就已确定,如非灶性不典型性和发育不良的开始,并在肿瘤存在时进一步增加。在光化性膀胱炎模型中,胶原纤维的线性化与 BBN 诱导的肿瘤较早发生有关。基质的地形重构可能是识别和治疗易复发肿瘤的非肿瘤性组织的标志物。
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来源期刊
Matrix Biology Plus
Matrix Biology Plus Medicine-Histology
CiteScore
9.00
自引率
0.00%
发文量
25
审稿时长
105 days
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