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颅面部骨肉瘤——骨生物学特征表达的初步研究及转移假说

Craniofacial Osteosarcoma-Pilot Study on the Expression of Osteobiologic Characteristics and Hypothesis on Metastasis.

作者信息

Weber Manuel, Söder Stephan, Sander Janina, Ries Jutta, Geppert Carol, Kesting Marco, Wehrhan Falk

机构信息

Department of Oral and Maxillofacial Surgery, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany.

Institute of Pathology, Fürth, Germany.

出版信息

Front Oncol. 2020 Jun 23;10:745. doi: 10.3389/fonc.2020.00745. eCollection 2020.

Abstract

Craniofacial osteosarcomas (COS) and extracranial osteosarcomas (EOS) show distinct clinical differences. COS show a remarkably lower incidence of metastases and a better survival. However, in contrast to EOS, they show a poor response to neoadjuvant chemotherapy. Tumor-associated macrophages and their polarization as well as developmental biological signaling pathways are possible candidates for explaining the clinical differences between COS and EOS. The aim of the study was to analyze differential expression of macrophage markers and important regulators of these pathways. Twenty osteosarcoma cases (10 COS and 10 EOS) were immunohistochemically stained to assess CD68, CD11c, CD163, MRC1, Gli1, and Gli2 expression. Statistical differences between COS and EOS were tested using the Mann-Whitney test. Additionally, the paper describes an example of multidisciplinary treatment of a patient suffering from COS and discusses the surgical challenges in treatment and rehabilitation of COS. COS showed a significantly ( < 0.05) increased infiltration of CD11c-positive M1 macrophages and a shift toward M1 polarization compared to EOS. Additionally, COS revealed a significantly ( < 0.05) lower Gli1 expression than EOS. The reduced Gli1 expression in COS can be interpreted as reduced activation of the Hedgehog (Hh) signaling pathway. The increased M1 polarization and reduced Hh activation in COS could explain the low incidence of metastases in these osteosarcomas.

摘要

颅面部骨肉瘤(COS)与颅外骨肉瘤(EOS)表现出明显的临床差异。COS的转移发生率显著较低,生存率更高。然而,与EOS不同的是,它们对新辅助化疗的反应较差。肿瘤相关巨噬细胞及其极化以及发育生物学信号通路可能是解释COS和EOS临床差异的候选因素。本研究的目的是分析巨噬细胞标志物和这些信号通路重要调节因子的差异表达。对20例骨肉瘤病例(10例COS和10例EOS)进行免疫组织化学染色,以评估CD68、CD11c、CD163、MRC1、Gli1和Gli2的表达。使用曼-惠特尼检验来检测COS和EOS之间的统计学差异。此外,本文还描述了一例COS患者的多学科治疗案例,并讨论了COS治疗和康复中的手术挑战。与EOS相比,COS显示CD11c阳性M1巨噬细胞浸润显著增加(<0.05),且向M1极化转变。此外,COS的Gli1表达显著低于EOS(<0.05)。COS中Gli1表达降低可解释为刺猬信号通路(Hh)激活减少。COS中M1极化增加和Hh激活减少可以解释这些骨肉瘤转移发生率较低的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b91a/7325581/f6f352351d04/fonc-10-00745-g0001.jpg

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