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双膦酸盐的抗肿瘤潜力。

Anti-tumor potential of bisphosphonates.

作者信息

Green J R

机构信息

Novartis Pharma AG, Basel, Switzerland.

出版信息

Med Klin (Munich). 2000 Oct 15;95 Suppl 2:23-8.

Abstract

In addition to inhibiting bone resorption, bisphosphonates also exert anti-tumor effects. The most potent compounds are the newer, nitrogen-containing bisphosphonates such as zoledronic acid. In vitro, bisphosphonates inhibit proliferation and induce apoptosis in human tumor cell lines, and interfere with cell adhesion, invasion and growth factor secretion. The combination of bisphosphonates with other anti-cancer drugs such as paclitaxel or tamoxifen markedly enhances these effects. In vivo, zoledronic acid has recently been shown to inhibit angiogenesis. Although bisphosphonates are very effective against bone metastases, their in vivo anti-tumor potential against visceral metastases remains to be explored.

摘要

除了抑制骨吸收外,双膦酸盐还具有抗肿瘤作用。最有效的化合物是较新的含氮双膦酸盐,如唑来膦酸。在体外,双膦酸盐可抑制人肿瘤细胞系的增殖并诱导其凋亡,还可干扰细胞黏附、侵袭及生长因子分泌。双膦酸盐与其他抗癌药物(如紫杉醇或他莫昔芬)联合使用可显著增强这些作用。在体内,最近研究表明唑来膦酸可抑制血管生成。尽管双膦酸盐对骨转移非常有效,但其对内脏转移的体内抗肿瘤潜力仍有待探索。

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