独特的细胞类型特异性信号模式定义胆脂瘤。

IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY
Christopher M Welch, Shuze Wang, Joerg Waldhaus
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引用次数: 0

摘要

目的:确定驱动胆脂瘤的细胞类型和信号通路。方法:采用单细胞RNA测序(scRNA-seq)技术鉴定人胆脂瘤标本与先前发表的正常人鼓膜scRNA-seq数据之间的差异。CellChat算法确定了两种组织之间的差异信号通路。利用免疫组织化学方法在人胆脂瘤标本上验证胆脂瘤特异性标记物。背景:胆脂瘤是一种复杂的、扩张的、破坏性的囊性上皮病变,发生在颞骨内。它破坏周围组织,导致严重的耳科并发症。目前,唯一的治疗选择是手术切除疾病,尽管手术治疗,十年后手术后复发或残留的胆脂瘤率接近40%至50%。广泛的研究试图通过描绘驱动胆脂瘤行为的信号通路来产生医学治疗,并确定了许多途径。然而,胆脂瘤药物治疗的进展一直受到固有细胞异质性的阻碍,细胞类型特异性行为被组织的大量分析所掩盖。结果:胆脂瘤细胞组成与正常鼓膜明显不同,胆脂瘤免疫细胞数量增加。许多细胞信号通路在胆脂瘤和正常组织之间也有不同的调节,包括几种生长因子、Wnt、白细胞介素、细胞粘附和肿瘤坏死因子通路,在胆脂瘤中具有独特的细胞类型特异性模式。结论:scRNA-seq数据定义了胆脂瘤的细胞组成和细胞类型特异性信号通路,从而确定潜在的药物靶点,并为未来改善该疾病的治疗策略提供信息。专业实践差距和教育需求:对胆脂瘤的分子理解仍然很差,导致缺乏针对这种相对常见和麻烦的疾病的医学治疗。学习目的:明确胆脂瘤相对于正常鼓膜的细胞特征和细胞类型特异性信号通路。期望结果:确定胆脂瘤中独特的细胞类型特异性信号通路,这可能需要进一步评估作为胆脂瘤医学治疗的潜在治疗靶点。证据水平:不适用于硅细胞研究。irb或iacuc: irb HUM00153531。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unique Cell Type-Specific Signaling Patterns Define Cholesteatoma.

Objective: To identify cell types and signaling pathways that drive cholesteatoma.

Methods: Single-cell RNA sequencing (scRNA-seq) was applied to identify differences between human cholesteatoma specimens and previously published scRNA-seq data for normal human tympanic membrane. The CellChat algorithm determined differential signaling pathways between both tissues. Cholesteatoma-specific markers were validated utilizing immunohistochemistry on human cholesteatoma specimens.

Background: Cholesteatoma is a complex, expansile, and destructive cystic epithelial lesion that occurs within the temporal bone. It destroys surrounding tissue, leading to significant otologic complications. Currently, the only treatment option is surgical removal of the disease, and despite surgical treatment, rates of recurrent or residual cholesteatoma following surgery approach 40% to 50% a decade later. Extensive research has attempted to generate medical treatments by delineating signaling pathways that drive cholesteatoma behavior, with numerous pathways identified. However, progress in developing pharmacologic treatment of cholesteatoma has been hampered by the inherent cellular heterogeneity, with cell type-specific behaviors obscured by bulk analysis of tissue.

Results: Cholesteatoma cellular composition differs notably from normal tympanic membrane, with increased numbers of immune cells in cholesteatoma. A number of cell signaling pathways are also differentially regulated between cholesteatoma and normal tissues, including several growth factors, Wnt, interleukin, cell adhesion, and tumor necrosis factor pathways, with unique cell type-specific patterns in cholesteatoma.

Conclusions: scRNA-seq data define the cellular composition and cell type-specific signaling pathways in cholesteatoma, thereby identifying potential drug targets and informing future strategies to improve treatment of the disease.

Professional practice gap and educational need: The molecular understanding of cholesteatoma remains poor, resulting in a lack of medical treatments for this relatively common and troublesome condition.

Learning objective: To define the cellular profile and cell type-specific signaling pathways of cholesteatoma relative to normal tympanic membrane.

Desired result: To define the unique cell type-specific signaling pathways within cholesteatoma that may warrant further evaluation as potential therapeutic targets for medical treatment of cholesteatoma.

Level of evidence: Not applicable, in silico cellular study.

Indicate irb or iacuc: IRB HUM00153531.

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来源期刊
Otology & Neurotology
Otology & Neurotology 医学-耳鼻喉科学
CiteScore
3.80
自引率
14.30%
发文量
509
审稿时长
3-6 weeks
期刊介绍: ​​​​​Otology & Neurotology publishes original articles relating to both clinical and basic science aspects of otology, neurotology, and cranial base surgery. As the foremost journal in its field, it has become the favored place for publishing the best of new science relating to the human ear and its diseases. The broadly international character of its contributing authors, editorial board, and readership provides the Journal its decidedly global perspective.
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