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表皮调节素通过ERK1/2信号通路诱导人SK-N-BE细胞分化。

Epiregulin induces human SK-N-BE cell differentiation through ERK1/2 signaling pathway.

作者信息

Rizzi Manuela, Pittarella Pamela, Sabbatini Maurizio, Renò Filippo

机构信息

Health Sciences Department, University of Eastern Piedmont A. Avogadro, Via Solaroli 17, 28100 Novara, Italy.

出版信息

Growth Factors. 2013 Jun;31(3):90-7. doi: 10.3109/08977194.2013.795958.

Abstract

Epidermal growth factor (EGF) and other EGF-related growth factors, such as transforming growth factor-α, are able to stimulate neuroblastoma (NB) cell proliferation. Epiregulin (Epi) is a growth factor belonging to the EGF family known to be more potent than EGF in mediating mitogenic signals. In this study, we tested the ability of Epi to stimulate a human NB cell line (SK-N-BE) proliferation. Surprisingly, Epi (50-1000 ng/ml) induced a reduction in SK-N-BE proliferation along with a morphological differentiation, associated with an increase in MMP-9 expression. Moreover, Epi-induced differentiation was inhibited by ERK1/2 phosphorilation inhibition. In conclusion, Epi could represent a novel and useful tool to oppose NB cell proliferation.

摘要

表皮生长因子(EGF)以及其他与EGF相关的生长因子,如转化生长因子-α,能够刺激神经母细胞瘤(NB)细胞增殖。上皮调节素(Epi)是一种属于EGF家族的生长因子,已知在介导有丝分裂信号方面比EGF更有效。在本研究中,我们测试了Epi刺激人NB细胞系(SK-N-BE)增殖的能力。令人惊讶的是,Epi(50-1000 ng/ml)诱导SK-N-BE增殖减少,并伴有形态学分化,同时MMP-9表达增加。此外,ERK1/2磷酸化抑制可抑制Epi诱导的分化。总之,Epi可能是对抗NB细胞增殖的一种新型且有用的工具。

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