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细胞间接触增强了表皮生长因子受体(EGFR)和信号转导子和转录激活子 3(STAT3)的激活,从而增加了足细胞蛋白的表达,以促进鳞状细胞癌的迁移。

Intercellular contact augments epidermal growth factor receptor (EGFR) and signal transducer and activator of transcription 3 (STAT3)-activation which increases podoplanin-expression in order to promote squamous cell carcinoma motility.

机构信息

Department of Dermatology, Asahikawa Medical University, Midorigaoka-Higashi 2-1-1-1, Asahikawa, Japan.

出版信息

Cell Signal. 2013 Apr;25(4):760-5. doi: 10.1016/j.cellsig.2012.12.004. Epub 2012 Dec 22.

Abstract

The transmembrane glycoprotein podoplanin (PDPN) plays an important role in cell motility. However, mechanisms regulating PDPN expression have not been fully elucidated. Here, we investigated the effect of intercellular contact on signal transduction pathways and PDPN expression in human squamous cell carcinoma (SCC) cell lines. PDPN expression was higher in confluent SCC cells than sparse cultures. This PDPN induction leads to increased SCC cell migration and invasion, which was reversed by shRNA PDPN knockdown. This cell density dependent PDPN induction required activation of epidermal growth factor receptor (EGFR) and its effector, signal transducer and activator of transcription 3 (STAT3). These observations also extend to human clinical specimens, in which PDPN expression localized to confluent basal cell layers at the invading front of in situ SCC lesions. Taken together, these results illuminate an EGFR-STAT3-PDPN pathway as a potential pharmacological opportunity to target invasive SCC cells.

摘要

跨膜糖蛋白 podoplanin(PDPN)在细胞运动中发挥重要作用。然而,调节 PDPN 表达的机制尚未完全阐明。在这里,我们研究了细胞间接触对人鳞状细胞癌(SCC)细胞系中信号转导途径和 PDPN 表达的影响。在致密培养的 SCC 细胞中 PDPN 的表达高于稀疏培养。这种 PDPN 的诱导导致 SCC 细胞迁移和侵袭增加,而 shRNA PDPN 敲低可逆转这种作用。这种细胞密度依赖性 PDPN 诱导需要表皮生长因子受体(EGFR)及其效应子信号转导和转录激活因子 3(STAT3)的激活。这些观察结果也扩展到人类临床标本,其中 PDPN 表达定位于原位 SCC 病变侵袭前沿的致密基底细胞层。总之,这些结果阐明了 EGFR-STAT3-PDPN 通路是靶向侵袭性 SCC 细胞的潜在药物靶点。

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