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双膦酸盐的抗肿瘤潜力。

The antitumor potential of bisphosphonates.

作者信息

Clézardin Philippe

机构信息

Laënnec School of Medicine, Lyon, France.

出版信息

Semin Oncol. 2002 Dec;29(6 Suppl 21):33-42. doi: 10.1053/sonc.2002.37420.

Abstract

Bisphosphonates are primarily known for their ability to inhibit osteoclast-mediated bone resorption and to slow the release of calcium and other bone minerals into the blood stream. However, recent preclinical research has shown that bisphosphonates also exhibit potent antitumor activity. Bisphosphonates reduce proliferation and induce apoptosis of tumor cell lines, and they inhibit tumor cell adhesion and invasion of the extracellular matrix in vitro. In addition, bisphosphonates have been shown to reduce skeletal tumor burden in a variety of animal models. This may reflect either direct antitumor effects or indirect effects via osteoclast inhibition and alteration of the bone microenvironment. The complex mechanisms by which bisphosphonates inhibit bone resorption and interfere with tumor growth and metastasis to bone are beginning to be understood. Research is ongoing to fully elucidate these biochemical mechanisms, and well-designed clinical trials are planned to investigate the antitumor potential of modern nitrogen-containing bisphosphonates in the clinical setting.

摘要

双膦酸盐主要因其抑制破骨细胞介导的骨吸收以及减缓钙和其他骨矿物质释放到血流中的能力而闻名。然而,最近的临床前研究表明,双膦酸盐还具有强大的抗肿瘤活性。双膦酸盐可减少肿瘤细胞系的增殖并诱导其凋亡,并且在体外抑制肿瘤细胞黏附和侵袭细胞外基质。此外,在多种动物模型中已证明双膦酸盐可减轻骨骼肿瘤负担。这可能反映了直接抗肿瘤作用或通过抑制破骨细胞和改变骨微环境的间接作用。双膦酸盐抑制骨吸收并干扰肿瘤生长和骨转移的复杂机制正开始被人们所理解。正在进行研究以充分阐明这些生化机制,并且计划开展精心设计的临床试验以研究现代含氮双膦酸盐在临床环境中的抗肿瘤潜力。

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