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CTGF 在恶性黑色素瘤中过表达,并促进细胞侵袭和迁移。

CTGF is overexpressed in malignant melanoma and promotes cell invasion and migration.

机构信息

University of Regensburg Medical School, Institute of Pathology, Franz-Josef-Strauss-Allee 11, Regensburg D-93053, Germany.

出版信息

Br J Cancer. 2011 Jul 12;105(2):231-8. doi: 10.1038/bjc.2011.226. Epub 2011 Jun 14.

Abstract

BACKGROUND

Malignant melanoma cells are known to have altered expression of growth factors compared with normal human melanocytes. These changes most likely favour tumour growth and progression, and influence tumour environment. The induction of transforming growth factor beta1, 2 and 3 as well as BMP4 and BMP7 expression in malignant melanoma has been reported before, whereas the expression of an important modulator of these molecules, connective tissue growth factor (CTGF), has not been investigated in melanomas until now.

METHODS

Expression of CTGF was analysed in melanoma cell lines and tissue samples by qRT-PCR and immunohistochemistry. To determine the regulation of CTGF expression in malignant melanoma, specific siRNA was used. Additionally, migration, invasion and attachment assays were carried out.

RESULTS

We were able to demonstrate that CTGF expression is upregulated in nine melanoma cell lines and in primary and metastatic melanoma in situ. The transcription factor HIF-1α was revealed as a positive regulator for CTGF expression. Melanoma cells, in which CTGF expression is diminished, show a strong reduction of migratory and invasive properties when compared with controls. Further, treatment of normal human epidermal melanocytes with recombinant CTGF leads to an increase of migratory and invasive behaviour of these cells.

CONCLUSION

These results suggest that CTGF promotes melanoma cell invasion and migration and, therefore, has an important role in the progression of malignant melanoma.

摘要

背景

与正常人类黑色素细胞相比,恶性黑色素瘤细胞的生长因子表达发生改变。这些变化很可能有利于肿瘤的生长和进展,并影响肿瘤微环境。先前已经报道了恶性黑色素瘤中转化生长因子 beta1、2 和 3 以及 BMP4 和 BMP7 的诱导表达,而到目前为止,这些分子的重要调节剂结缔组织生长因子(CTGF)在黑色素瘤中的表达尚未被研究。

方法

通过 qRT-PCR 和免疫组织化学分析黑色素瘤细胞系和组织样本中的 CTGF 表达。为了确定 CTGF 在恶性黑色素瘤中的表达调控,使用了特定的 siRNA。此外,还进行了迁移、侵袭和附着测定。

结果

我们能够证明 CTGF 在九种黑色素瘤细胞系以及原位原发性和转移性黑色素瘤中表达上调。转录因子 HIF-1α 被揭示为 CTGF 表达的正调节剂。与对照相比,CTGF 表达减少的黑素瘤细胞的迁移和侵袭特性明显降低。此外,用重组 CTGF 处理正常人表皮黑色素细胞会导致这些细胞的迁移和侵袭行为增加。

结论

这些结果表明 CTGF 促进黑色素瘤细胞的侵袭和迁移,因此在恶性黑色素瘤的进展中具有重要作用。

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