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一种基于算法的技术,用于通过福尔马林固定和石蜡包埋切片的免疫组织化学染色来计数细胞中的线粒体。

An algorithm-based technique for counting mitochondria in cells using immunohistochemical staining of formalin-fixed and paraffin-embedded sections.

机构信息

Division of Biomarker Discovery, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Chiba, Japan.

Department of Pathology, Saitama Cancer Center, Saitama, Japan.

出版信息

J Cancer Res Clin Oncol. 2024 Apr 3;150(4):172. doi: 10.1007/s00432-024-05653-1.

Abstract

PURPOSE

Visualizing mitochondria in cancer cells from human pathological specimens may improve our understanding of cancer biology. However, using immunohistochemistry to evaluate mitochondria remains difficult because almost all cells contain mitochondria and the number of mitochondria per cell may have important effects on mitochondrial function. Herein, we established an objective system (Mito-score) for evaluating mitochondria using machine-based processing of hue, saturation, and value color spaces.

METHODS

The Mito-score was defined as the number of COX4 (mitochondrial inner membrane) immunohistochemistry-positive pixels divided by the number of nuclei per cell. The system was validated using four lung cancer cell lines, normal tissues, and lung cancer tissues (199 cases).

RESULTS

The Mito-score correlated with MitoTracker, a fluorescent dye used to selectively label and visualize mitochondria within cells under a microscope (R = 0.68) and with the number of mitochondria counted using electron microscopy (R = 0.79). Histologically, the Mito-score of small cell carcinoma (57.25) was significantly lower than that of adenocarcinoma (147.5, p < 0.0001), squamous cell carcinoma (120.6, p = 0.0004), and large cell neuroendocrine carcinoma (111.8, p = 0.002).

CONCLUSION

The Mito-score method enables the analysis of the mitochondrial status of human formalin-fixed paraffin-embedded specimens and may provide insights into the metabolic status of cancer.

摘要

目的

从人体病理标本中可视化癌细胞中的线粒体,可以增进我们对癌症生物学的理解。然而,使用免疫组织化学来评估线粒体仍然具有挑战性,因为几乎所有细胞都含有线粒体,并且每个细胞中的线粒体数量可能对线粒体功能具有重要影响。在此,我们建立了一种使用基于机器的色调、饱和度和值颜色空间处理来评估线粒体的客观系统(Mito-score)。

方法

Mito-score 定义为 COX4(线粒体内膜)免疫组织化学阳性像素数除以每个细胞的细胞核数。该系统使用四个肺癌细胞系、正常组织和肺癌组织(199 例)进行了验证。

结果

Mito-score 与 MitoTracker 相关,MitoTracker 是一种荧光染料,用于在显微镜下选择性标记和可视化细胞内的线粒体(R=0.68),并与使用电子显微镜计数的线粒体数量相关(R=0.79)。组织学上,小细胞癌(57.25)的 Mito-score 明显低于腺癌(147.5,p<0.0001)、鳞状细胞癌(120.6,p=0.0004)和大细胞神经内分泌癌(111.8,p=0.002)。

结论

Mito-score 方法能够分析人福尔马林固定石蜡包埋标本中的线粒体状态,并可能深入了解癌症的代谢状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f94/11793318/f9c8e1a3eb4d/432_2024_5653_Fig1_HTML.jpg

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