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杂交脂质体抑制鼠骨肉瘤细胞的肿瘤生长和肺转移。

Hybrid liposomes inhibit tumor growth and lung metastasis of murine osteosarcoma cells.

机构信息

Division of Applied Life Science, Graduate School of Engineering, Sojo University, Kumamoto, Japan.

出版信息

Cancer Med. 2013 Jun;2(3):267-76. doi: 10.1002/cam4.67. Epub 2013 Mar 22.

Abstract

Antitumor effects of hybrid liposomes (HL) composed of l-α-dimyristoylphosphatidylcholine (DMPC) and polyoxyethylene(23) dodecyl ether (C₁₂(EO)₂₃) on the metastatic growth of murine osteosarcoma (LM8) cells were investigated in vitro and in vivo. Remarkable inhibitory effects of HL-23 on the growth of LM8 cells were obtained through the induction of apoptotic cell death in vitro. It was also indicated that HL-23 should dramatically suppress the invasion of LM8 cells and the formation of filopodia on the cell surface in vitro. Furthermore, significantly high therapeutic effects were observed in the homograft mouse models of LM8 cells with lung metastasis after the treatment with HL-23 in vivo. That is, the histological analysis demonstrated that the primary tumor growth of LM8 cells implanted subcutaneously into the mice was inhibited along with the induction of apoptosis. In addition, it was found that HL-23 significantly decreased the lung metastasis of LM8 cells in the mouse models through the inhibition of primary tumor invasion. These results suggest that HL-23 could be a novel agent for the chemotherapy of osteosarcoma.

摘要

杂交脂质体(HL)由 l-α-二肉豆蔻酰磷脂酰胆碱(DMPC)和聚氧乙烯(23)十二烷基醚(C₁₂(EO)₂₃)组成,研究了其对体外和体内小鼠骨肉瘤(LM8)细胞转移生长的抗肿瘤作用。HL-23 在体外诱导细胞凋亡,对 LM8 细胞的生长具有显著的抑制作用。此外,HL-23 还能显著抑制 LM8 细胞的侵袭和细胞表面丝状伪足的形成。此外,体内给予 HL-23 后,在 LM8 细胞肺转移的同种异体移植小鼠模型中观察到显著的治疗效果。即组织学分析表明,HL-23 可通过诱导细胞凋亡抑制皮下植入小鼠的 LM8 细胞的原发性肿瘤生长。此外,发现 HL-23 通过抑制原发性肿瘤侵袭,显著减少了小鼠模型中 LM8 细胞的肺转移。这些结果表明,HL-23 可能成为骨肉瘤化疗的一种新型药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e31e/3699838/3787eca2c253/cam40002-0267-f1.jpg

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