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骨肉瘤来源的小细胞外囊泡通过miR-146a-5p增强肿瘤转移并抑制破骨细胞生成。

Osteosarcoma-Derived Small Extracellular Vesicles Enhance Tumor Metastasis and Suppress Osteoclastogenesis by miR-146a-5p.

作者信息

Araki Yoshihiro, Aiba Hisaki, Yoshida Takeshi, Yamamoto Norio, Hayashi Katsuhiro, Takeuchi Akihiko, Miwa Shinji, Igarashi Kentaro, Nguyen Tuan D, Ishii Kiyo-Aki, Nojima Takayuki, Takahashi Satoru, Murakami Hideki, Tsuchiya Hiroyuki, Hanayama Rikinari

机构信息

Department of Immunology, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.

Department of Orthopaedic Surgery, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.

出版信息

Front Oncol. 2021 May 4;11:667109. doi: 10.3389/fonc.2021.667109. eCollection 2021.

Abstract

Osteosarcoma is the most frequent type of primary bone tumor in children and adolescents, thus care for patients with malignant osteosarcoma is strongly required. The roles of small extracellular vesicles (SEVs) in enhancing metastases have been demonstrated in multiple tumors, but they are still poorly understood in osteosarcoma. Hence, this study investigated the effects of SEVs on progression and the tumor microenvironment in mice and patients. In an orthotopic implantation study, we found that osteosarcoma-derived SEVs had the potential to enhance metastases and angiogenesis. In addition, osteosarcoma-derived SEVs decreased the number of mature osteoclasts . osteoclastogenesis studies revealed that the inhibition of osteoclast maturation by osteosarcoma-derived SEVs was mediated by suppressing the NF-κB signal pathway. MicroRNA analysis of SEVs from different malignant human osteosarcomas revealed that miR-146a-5p was involved in the inhibition of osteoclastogenesis. In osteosarcoma patients, lower numbers of osteoclasts in biopsy specimens at the first visits were correlated with higher malignancy. These findings indicated that osteosarcoma-derived SEVs enhance distant metastasis of osteosarcomas by inhibiting osteoclast maturation, which may be a useful prognostic marker. This diagnostic method may enable to predict malignancy at early stage, and help to provide optimal care to patients with risk of high malignancy.

摘要

骨肉瘤是儿童和青少年中最常见的原发性骨肿瘤类型,因此对恶性骨肉瘤患者的护理需求迫切。小细胞外囊泡(SEVs)在多种肿瘤中促进转移的作用已得到证实,但在骨肉瘤中的作用仍知之甚少。因此,本研究调查了SEVs对小鼠和患者肿瘤进展及肿瘤微环境的影响。在原位植入研究中,我们发现骨肉瘤来源的SEVs具有增强转移和血管生成的潜力。此外,骨肉瘤来源的SEVs减少了成熟破骨细胞的数量。破骨细胞生成研究表明,骨肉瘤来源的SEVs对破骨细胞成熟的抑制作用是通过抑制NF-κB信号通路介导的。对来自不同恶性人类骨肉瘤的SEVs进行的微小RNA分析显示,miR-146a-5p参与了对破骨细胞生成的抑制。在骨肉瘤患者中,初次就诊时活检标本中破骨细胞数量较少与较高的恶性程度相关。这些发现表明,骨肉瘤来源的SEVs通过抑制破骨细胞成熟来增强骨肉瘤的远处转移,这可能是一个有用的预后标志物。这种诊断方法可能有助于在早期预测恶性程度,并有助于为具有高恶性风险的患者提供最佳护理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43b6/8130824/d32825af4c0d/fonc-11-667109-g001.jpg

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