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强力霉素作为金属蛋白酶(MMP)抑制剂在骨肉瘤中的抗肿瘤作用:一项系统评价。

The anti-neoplastic effect of doxycycline in osteosarcoma as a metalloproteinase (MMP) inhibitor: a systematic review.

作者信息

Hadjimichael Argyris C, Foukas Athanasios F, Savvidou Olga D, Mavrogenis Andreas F, Psyrri Amanda K, Papagelopoulos Panayiotis J

机构信息

13rd Department of Orthopedic Surgery, KAT Hospital, Athens, Greece.

21st Department of Orthopedic Surgery, National and Kapodistrian University of Athens, Medical School, Attikon University hospital, Athens, Greece.

出版信息

Clin Sarcoma Res. 2020 Apr 30;10:7. doi: 10.1186/s13569-020-00128-6. eCollection 2020.

Abstract

BACKGROUND

Osteosarcoma is a very aggressive primary bone tumour, affecting mainly young populations. Most cases diagnosed have distant macro- and micro-metastases at the time of diagnosis. Surgical resection with neoadjuvant and adjuvant therapies improves the overall and disease-free survival of patients. Doxycycline, a synthetic tetracycline, has been found to act either as an antibiotic drug or as a chemotherapeutic agent. Its anti-neoplastic role has been found to be significant, in vitro and in vivo laboratory trials, in various types of cancer, such as prostate, intestinal, central neural system cancers and osteosarcoma. Inhibition of metalloproteinases (MMPs) in different stages of tumour expansion is the most well-understood mechanism. MMPs are secreted molecules from various normal cells, such as fibroblasts, leucocytes and vascular smooth muscles, as well as from cells with high proliferative potential, such as tumour cells. In osteosarcoma, MMPs have been found to be overexpressed. MMPs help osteosarcoma cells survive, grow and produce metastases in distant sites, mainly in the lungs. Doxycycline blocks extracellular matrix and basic membrane degradation by suppressing MMP function. As a consequence, osteosarcoma cells lose their ability to invade and metastasize. Additionally, doxycycline eliminates the secretion of vascular endothelial growth factor (VEGF) and deprives the supply of circulating nutrients by its anti-angiogenesis action. The aim of this review is to evaluate doxycycline's action against osteosarcoma cells as an MMP-inhibitor and interpret its usage as a chemotherapeutic agent.

METHODS

We checked PubMed and Google Scholar for recently published data, on the tumour-supportive role of MMPs and VEGF in osteosarcoma cells. We further studied published experimental trials on the role of doxycycline as a tumour-suppressive agent via MMPs and VEGF inhibition.

RESULTS

MMPs and VEGF have been found to play a fundamental role in osteosarcoma cells survival and high aggressiveness by in vitro, in vivo and clinical trials. Nevertheless, doxycycline has proved its tumour-suppressive effect by in vivo experimental trials in various cancers but not yet in osteosarcoma.

CONCLUSION

Doxycycline remains a promising chemotherapeutic agent against osteosarcoma via MMP inhibition, showing the need for further in vivo and clinical trials to be carried out in the future.

摘要

背景

骨肉瘤是一种侵袭性很强的原发性骨肿瘤,主要影响年轻人群。大多数确诊病例在诊断时已有远处宏观和微观转移。新辅助和辅助治疗的手术切除可提高患者的总生存率和无病生存率。强力霉素是一种合成四环素,已被发现可作为抗生素药物或化疗药物发挥作用。在体外和体内实验室试验中,其抗肿瘤作用在各种类型的癌症中都很显著,如前列腺癌、肠道癌、中枢神经系统癌和骨肉瘤。在肿瘤扩展的不同阶段抑制金属蛋白酶(MMPs)是最广为人知的机制。MMPs是由各种正常细胞分泌的分子,如成纤维细胞、白细胞和血管平滑肌细胞,以及具有高增殖潜能的细胞,如肿瘤细胞。在骨肉瘤中,已发现MMPs过度表达。MMPs有助于骨肉瘤细胞存活、生长并在远处转移,主要是肺部。强力霉素通过抑制MMP功能来阻止细胞外基质和基底膜的降解。因此,骨肉瘤细胞失去侵袭和转移能力。此外,强力霉素通过其抗血管生成作用消除血管内皮生长因子(VEGF)的分泌并剥夺循环营养物质的供应。本综述的目的是评估强力霉素作为MMP抑制剂对骨肉瘤细胞的作用,并解释其作为化疗药物的用途。

方法

我们在PubMed和谷歌学术上检索了最近发表的关于MMPs和VEGF在骨肉瘤细胞中的肿瘤支持作用的数据。我们进一步研究了已发表的关于强力霉素通过抑制MMPs和VEGF作为肿瘤抑制药物作用的实验性试验。

结果

通过体外实验、体内实验和临床试验发现,MMPs和VEGF在骨肉瘤细胞存活和高侵袭性中起重要作用。然而,强力霉素在各种癌症的体内实验中已证明其肿瘤抑制作用,但在骨肉瘤中尚未得到证实。

结论

强力霉素通过抑制MMPs仍然是一种有前景的抗骨肉瘤化疗药物,这表明未来需要进行进一步的体内实验和临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e59/7193389/cfcc854cae89/13569_2020_128_Fig1_HTML.jpg

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