宏观上黄色憎色性肾细胞癌与非黄色憎色性肾细胞癌的临床病理及分子特征比较。

IF 1.9 Q3 PATHOLOGY
Clinical Pathology Pub Date : 2021-12-12 eCollection Date: 2021-01-01 DOI:10.1177/2632010X211064821
Fumiyoshi Kojima, Ibu Matsuzaki, Naoto Kuroda, Yurina Mikasa, Fidele Y Musangile, Ryuta Iwamoto, Yuichi Takahashi, Akiko Matsubara, Yasuo Kohjimoto, Isao Hara, Shin-Ichi Murata
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引用次数: 0

摘要

肾细胞瘤的每一种组织学变异都有独特的颜色。透明细胞肾细胞癌(CCRCC)的淡黄色是由于存在胞浆内脂质和糖原积累。CCRCC的颜色变化与临床病理和代谢变化以及生物学行为有关。我们分析并比较了黄色ChRCC (ChRCC- y)、非黄色ChRCC (ChRCC- n)和CCRCC的脂质代谢的临床、组织病理学、免疫组织化学特征和基因表达谱。在14个chrcc中,我们检索到6个ChRCC-Ys。与ChRCC-N患者相比,ChRCC-Y患者更年轻,且该肿瘤在男性中并不占优势。ChRCC-Ys小于ChRRC-Ns。三个ChRCC-Ys表现出独立的离散小管形成。没有ChRCC-Ns表现出单独的离散小管形成。6例ChRCC-Ys中2例呈相对弥漫性亲脂素阳性。无ChRCC-Ns显示嗜脂素弥漫性阳性。SCD、FDFT1、E2F1在ChRCC-Y中的表达低于在ChRCC-N中的表达。PDGFB在ChRCC-Y中的表达有高于ChRCC-N的趋势。本研究表明,ChRCC-Y不显示脂质和胆固醇代谢的增加,并且ChRCC-Y不具有CCRCC常见的分子改变。在ChRCC-Y中缺乏这种代谢加速可能支持生物惰性行为。此外,我们从不同角度揭示了宏观颜色变化可能与各种临床病理特征以及免疫组织化学和分子变化有关。我们认为需要进一步表征RCC,包括肿瘤异质性,以改善RCC患者的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinicopathological and Molecular Characteristics of Macroscopically Yellowish-Colored Chromophobe Renal Cell Carcinoma Compared to Non-Yellowish-Colored Chromophobe Renal Cell Carcinoma.

Clinicopathological and Molecular Characteristics of Macroscopically Yellowish-Colored Chromophobe Renal Cell Carcinoma Compared to Non-Yellowish-Colored Chromophobe Renal Cell Carcinoma.

Clinicopathological and Molecular Characteristics of Macroscopically Yellowish-Colored Chromophobe Renal Cell Carcinoma Compared to Non-Yellowish-Colored Chromophobe Renal Cell Carcinoma.

Clinicopathological and Molecular Characteristics of Macroscopically Yellowish-Colored Chromophobe Renal Cell Carcinoma Compared to Non-Yellowish-Colored Chromophobe Renal Cell Carcinoma.

Each histological variant of renal cell tumors has a unique color. The yellowish color of clear cell renal cell carcinoma (CCRCC) is explained by the presence of intracytoplasmic lipid and glycogen accumulation. Color changes in CCRCC are correlated with clinicopathological and metabolic changes, as well as biological behavior. We analyzed and compared the clinical, histopathological, and immunohistochemical features and gene expression profiles, in lipid metabolism of yellowish-colored ChRCC (ChRCC-Y), non-yellowish-colored ChRCC (ChRCC-N), and CCRCC. Of 14 ChRCCs, we retrieved 6 ChRCC-Ys. Patients with ChRCC-Y are younger than those with ChRCC-N, and the tumor is not predominant in males. ChRCC-Ys are smaller than ChRRC-Ns. Three ChRCC-Ys exhibited individual discrete tubule formation. No ChRCC-Ns exhibited individual discrete tubule formation. Two of 6 ChRCC-Ys showed relatively diffuse adipophilin positivity. No ChRCC-Ns demonstrated diffuse positivity for adipophilin. The expression of SCD, FDFT1, and E2F1 showed a tendency to be lower in ChRCC-Y than in ChRCC-N. The expression of PDGFB showed a tendency to be higher in ChRCC-Y than in ChRCC-N. This study demonstrated ChRCC-Y did not indicate an increase in lipid and cholesterol metabolism and that ChRCC-Y did not have the common molecular alteration of CCRCC. The absence of such metabolic acceleration in ChRCC-Y might support the biological indolent behavior. Furthermore, we revealed that macroscopic color changes might be correlated with various clinicopathological features and immunohistochemical and molecular changes from different perspectives. We believe further characterization of RCC, including tumor heterogeneity, is needed to improve the management of patients with RCC.

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来源期刊
Clinical Pathology
Clinical Pathology PATHOLOGY-
CiteScore
2.20
自引率
7.70%
发文量
66
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