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DOI 10.1186/1756-9966-30-31

Медицинская библиотека · Journal of experimental & clinical cancer research : CR · 2011

Expression of Ets-1, Ang-2 and maspin in ovarian cancer and their role in tumor angiogenesis.

Lin Zijing, Liu Yu, Sun Yuhui, He Xiuping

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

Various angiogenic regulators are involved in angiogenesis cascade. Transcription factor Ets-1 plays important role in angiogenesis, remodeling of extracellular matrix, and tumor metastasis. Ets-1 target genes involved in various stages of new blood vessel formation include angiopoietin, matrix metalloproteinases (MMPs) and the protease inhibitor maspin.

METHODS

We used immunohistochemistry (IHC) to detect the expression of Ets-1, angiopoietin-2 (Ang-2) and maspin in ovarian tumor and analyzed the relationship between the expression of these proteins and the clinical manifestation of ovarian cancer.

RESULTS

Ets-1 expression was much stronger in ovarian cancer compared to benign tumors, but had no significant correlation with other pathological parameters of ovarian cancer. However, Ang-2 and maspin expression had no obvious correlation with pathological parameters of ovarian cancer. Ets-1 had a positive correlation with Ang-2 which showed their close relationship in angiogenesis. Although microvessel density (MVD) value had no significant correlation with the expression of Ets-1, Ang-2 or maspin, strong nuclear expression of maspin appeared to be correlated with high grade and MVD.

CONCLUSIONS

The expression of Ets-1, Ang2 and maspin showed close relationship with angiogenesis in ovarian cancer and expression of maspin appeared to be correlated with high grade and MVD. The mechanisms underlying the cross-talk of the three factors need further investigations.

Для цитирования: Lin Zijing, Liu Yu, Sun Yuhui, He Xiuping. Expression of Ets-1, Ang-2 and maspin in ovarian cancer and their role in tumor angiogenesis.. Journal of experimental & clinical cancer research : CR. 2011. DOI: 10.1186/1756-9966-30-31.

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