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自噬和核形态计量与食管鳞癌的组织病理学特征相关。

Autophagy and nuclear morphometry are associated with histopathologic features in esophageal squamous cell carcinoma.

机构信息

Graduate Program in Gastroenterology and Hepatology, Faculty of Medical Sciences, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Rio Grande do Sul, Brazil.

Hospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil.

出版信息

J Mol Med (Berl). 2024 Jan;102(1):39-52. doi: 10.1007/s00109-023-02387-4. Epub 2023 Oct 25.

Abstract

Less than 15% of patients with esophageal squamous cell carcinoma (ESCC) survive 5 years after diagnosis. A better understanding of the biology of these tumors and the development of clinical biomarkers is needed. Autophagy is a physiological mechanism involved in the turnover of cellular components that plays a key role in cancer. This study evaluated the differential levels of three key regulators of autophagy (SQSTM1, MAP1LC3B, and BECN1) in patients with ESCC, associating autophagy with histopathologic features, including the grade of differentiation, mitotic rate, inflammation score, and the intensity of tumor-infiltrating lymphocytes. Nuclear morphometry of the tumor parenchyma was also assessed, associating it with autophagy and histopathology. All three markers significantly increased in patients with ESCC compared to the control group. Based on the mean expression of each protein in the control group, 57% of patients with ESCC had high levels of all three markers compared to control patients (14%). The most frequent profiles found in ESCC were BECN/MAP1LC3 and BECN/SQSTM1. According to the TCGA database, we found that the main autophagy genes were upregulated in ESCC. Moreover, high levels of autophagy markers were associated with a poor prognosis. Considering nuclear morphometry, ESCC samples showed a significant reduction in nuclear area, which was strongly negatively correlated with autophagy. Finally, the percentage of normal nuclei was associated with tumor differentiation, while poorly differentiated tumors showed lower SQSTM1 levels. ESCC progression may involve increased autophagy and changes in nuclear structure, associated with clinically relevant histopathological features. KEY MESSAGES: Autophagy markers are co-increased in primary ESCC. Autophagy negatively correlates with nuclear morphometry in ESCC parenchyma. Autophagy and nuclear morphometry are associated with histopathological features. Autophagy is increased in ESCC-TCGA database and associated with poor prognosis.

摘要

食管鳞状细胞癌(ESCC)患者的 5 年生存率不足 15%。需要更好地了解这些肿瘤的生物学特性,并开发临床生物标志物。自噬是参与细胞成分周转的生理机制,在癌症中起着关键作用。本研究评估了 ESCC 患者中三种自噬关键调节因子(SQSTM1、MAP1LC3B 和 BECN1)的差异水平,将自噬与组织病理学特征(包括分化程度、有丝分裂率、炎症评分和肿瘤浸润淋巴细胞强度)相关联。还评估了肿瘤实质的核形态计量学,并将其与自噬和组织病理学相关联。与对照组相比,所有三种标志物在 ESCC 患者中均显著升高。根据对照组中每种蛋白质的平均表达,与对照组患者(14%)相比,57%的 ESCC 患者的三种标志物水平均较高。在 ESCC 中最常见的模式是 BECN/MAP1LC3 和 BECN/SQSTM1。根据 TCGA 数据库,我们发现 ESCC 中主要的自噬基因上调。此外,自噬标志物高水平与预后不良相关。考虑到核形态计量学,ESCC 样本显示核面积显著减小,与自噬呈强烈负相关。最后,正常核的百分比与肿瘤分化相关,而分化程度较低的肿瘤 SQSTM1 水平较低。ESCC 的进展可能涉及自噬增加和核结构改变,与临床相关的组织病理学特征相关。

关键信息

自噬标志物在原发性 ESCC 中共同升高。自噬与 ESCC 实质的核形态计量学呈负相关。自噬和核形态计量学与组织病理学特征相关。ESCC-TCGA 数据库中自噬增加,与预后不良相关。

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