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[基质金属蛋白酶-2活性与成釉细胞瘤细胞增殖和生长的关联]

[Association of matrix metalloproteinase-2 activity with cell proliferation and growth in ameloblastoma].

作者信息

Zhang Bin, Huang Hong-Zhang, Tao Qian, Liu Xi-Qiang, Wei Jing

机构信息

Department of Oral and Maxillofacial Surgery, The Second Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510120, China.

出版信息

Hua Xi Kou Qiang Yi Xue Za Zhi. 2006 Feb;24(1):7-10.

Abstract

OBJECTIVE

To investigate the relationship between matrix metalloproteinase-2 (MMP-2)activity and cell proliferation, growth and invasion of ameloblastoma.

METHODS

The cells and xenograft of ameloblastoma were treated with MMP-2 inhibitor Ro31-9790 and the effects of Ro31-9790 on the cell proliferation and growth of ameloblastoma were observed. Primary culture in vitro, subcapsular kidney xenograft in vivo, MTT assay, flow cytometry, neoplastic volume measurement and histochemistry were employed to study the effects of cell proliferation and growth produced by Ro31-9790.

RESULTS

There was no significant different in cell proliferation at same interval among several groups (P > 0.05). The ratio of G0/G1 stage, G2/M stage and apoptotic cells didn't increase following increased Ro31-9790, and the ratio of S stage cells also didn't reduce following increased Ro31-9790. The tumor volume and its increase in treatment group were significant less than those in control group.

CONCLUSION

Ro31-9790 does not influence proliferation of ameloblastoma cells in vitro, but it can effectively inhibit the ameloblastoma growth in vivo. MMP-2 activity has no relationship to proliferation of ameloblastoma cells, but it can contribute to the ameloblastoma growth and may be a reason of invasion in ameloblastoma.

摘要

目的

探讨基质金属蛋白酶-2(MMP-2)活性与成釉细胞瘤细胞增殖、生长及侵袭之间的关系。

方法

用MMP-2抑制剂Ro31-9790处理成釉细胞瘤细胞及移植瘤,观察Ro31-9790对成釉细胞瘤细胞增殖和生长的影响。采用体外原代培养、体内肾包膜下移植、MTT法、流式细胞术、肿瘤体积测量及组织化学等方法研究Ro31-9790对细胞增殖和生长的影响。

结果

各组在相同时间间隔内细胞增殖无显著差异(P>0.05)。随着Ro31-9790浓度增加,G0/G1期、G2/M期细胞比例及凋亡细胞比例未增加,S期细胞比例也未减少。治疗组肿瘤体积及其增长明显小于对照组。

结论

Ro31-9790在体外不影响成釉细胞瘤细胞的增殖,但能有效抑制体内成釉细胞瘤的生长。MMP-2活性与成釉细胞瘤细胞的增殖无关,但可促进成釉细胞瘤的生长,可能是成釉细胞瘤侵袭的原因之一。

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