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4-甲基伞形酮通过黑素瘤细胞衍生因子抑制肿瘤细胞生长和基质透明质酸合成的激活。

4-Methylumbelliferone inhibits tumour cell growth and the activation of stromal hyaluronan synthesis by melanoma cell-derived factors.

机构信息

Section of Dermatology, Division of Cancer Sciences and Molecular Pathology, Faculty of Medicine, The Robertson Building, University of Glasgow, Glasgow G12 8QQ, UK.

出版信息

Br J Dermatol. 2010 Jun;162(6):1224-32. doi: 10.1111/j.1365-2133.2010.09699.x. Epub 2010 Feb 15.

Abstract

BACKGROUND

There is a close correlation between tumour progression and hyaluronan production, either by tumour cells or by stromal cells that are stimulated by tumour-derived factors. Inhibition of tumour stimulation of fibroblast hyaluronan may suppress tumour growth and invasion.

OBJECTIVES

To examine the effect of the hyaluronan synthesis inhibitor 4-methylumbelliferone (4-MU) on the growth of and hyaluronan synthesis by fibroblasts and C8161 and MV3 melanoma cell lines, invasion, and inhibition of tumour cell-derived factor activation of fibroblasts.

METHODS

Effects of 4-MU on growth and hyaluronan synthesis by fibroblasts and melanoma cells were examined in monolayer culture and fibroblast-contracted collagen lattices, and their effects on the growth and invasion of tumour cells into collagen lattices were also studied.

RESULTS

4-MU caused a dose-dependent growth inhibition of fibroblast and melanoma cells with maximum inhibition at 0·5 mmol L(-1) 4-MU. At this dose, 4-MU inhibited (3) H-glucosamine incorporation into fibroblast glycosaminoglycans by 52%, and hyaluronan synthesis by 64%. The relative inhibition was more pronounced when fibroblasts were stimulated with C8161 melanoma cell-conditioned medium. 4-MU reduced the level of hyaluronan in fibroblast-contracted collagen lattices, and inhibited both the growth on and invasion into the lattices by melanoma cells. This growth inhibition appears to be predominantly independent of inhibition of hyaluronan synthesis. The effect on growth inhibition was reversible, and 4-MU had no effect on apoptosis.

CONCLUSIONS

4-MU is a potent inhibitor of hyaluronan synthesis, induction of stromal hyaluronan accumulation by tumour cells, and fibroblast and melanoma cell proliferation, and results suggest that 4-MU may have potential as a tumour cell anti-invasive and antiproliferative agent.

摘要

背景

肿瘤的进展与透明质酸的产生密切相关,透明质酸可以由肿瘤细胞产生,也可以由受肿瘤衍生因子刺激的基质细胞产生。抑制肿瘤刺激纤维母细胞透明质酸的合成可能会抑制肿瘤的生长和侵袭。

目的

研究透明质酸合成抑制剂 4-甲基伞形酮(4-MU)对纤维母细胞和 C8161、MV3 黑色素瘤细胞系生长及透明质酸合成、侵袭的影响,以及对肿瘤细胞衍生因子激活纤维母细胞的抑制作用。

方法

在单层培养和纤维母细胞收缩的胶原格子中,观察 4-MU 对纤维母细胞和黑色素瘤细胞生长及透明质酸合成的影响,并研究其对肿瘤细胞侵入胶原格子生长和侵袭的影响。

结果

4-MU 呈剂量依赖性抑制纤维母细胞和黑色素瘤细胞的生长,在 0.5mmol/L 4-MU 时达到最大抑制。在该剂量下,4-MU 抑制(3)H-葡萄糖胺掺入纤维母细胞糖胺聚糖 52%,抑制透明质酸合成 64%。当纤维母细胞受到 C8161 黑色素瘤细胞条件培养基刺激时,相对抑制作用更为明显。4-MU 降低了纤维母细胞收缩的胶原格子中的透明质酸水平,并抑制了黑色素瘤细胞在格子上的生长和侵袭。这种生长抑制似乎主要与抑制透明质酸合成无关。该作用的抑制效果是可逆的,4-MU 对细胞凋亡没有影响。

结论

4-MU 是透明质酸合成、肿瘤细胞诱导基质透明质酸积累以及纤维母细胞和黑色素瘤细胞增殖的有效抑制剂,表明 4-MU 可能具有作为肿瘤细胞抗侵袭和抗增殖剂的潜力。

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