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EMMPRIN 有助于体外侵袭人涎腺腺样囊性癌细胞。

EMMPRIN contributes to the in vitro invasion of human salivary adenoid cystic carcinoma cells.

机构信息

Department of Oral and Maxillofacial Surgery, School of Stomatology, the Fourth Military Medical University, Xi'an 710032, PR China.

出版信息

Oncol Rep. 2012 Apr;27(4):1123-7. doi: 10.3892/or.2011.1606. Epub 2011 Dec 22.

Abstract

Extracellular matrix metalloproteinase inducer (EMMPRIN) is a transmembrane glycoprotein that is involved in tumor invasion by stimulating matrix metalloproteinase (MMP) expression. Our previous immunohistochemical study found that the expression of EMMPRIN in salivary adenoid cystic carcinoma (SACC) was positively correlated with tumor perineural and perivascular invasion. The present study was designed to further investigate the role of EMMPRIN in the invasion of SACC. Western blot results showed that EMMPRIN was upregulated in the highly metastatic SACC cell line SACC-LM, compared to SACC-83, a SACC cell line with low metastatic ability. Blocking of EMMPRIN by its antibody significantly decreased the adhesion, secretion of MMP-2 and MMP-9, and invasion activity of SACC-LM cells in vitro (P<0.01). Co-cultures of SACC-LM cells with fibroblasts significantly produced elevated levels of MMP-2 and MMP-9, and promoted the in vitro invasion activity of SACC-LM cells, compared with cultures of SACC-LM cells alone (P<0.01). These results indicate that EMMPRIN may play an important role in the invasion of SACC by stimulating the expression of MMP-2 and MMP-9 in tumor and stromal cells.

摘要

细胞外基质金属蛋白酶诱导因子(EMMPRIN)是一种跨膜糖蛋白,通过刺激基质金属蛋白酶(MMP)的表达参与肿瘤的侵袭。我们之前的免疫组织化学研究发现,唾液腺腺样囊性癌(SACC)中 EMMPRIN 的表达与肿瘤神经周围和血管周围侵袭呈正相关。本研究旨在进一步探讨 EMMPRIN 在 SACC 侵袭中的作用。Western blot 结果显示,与低转移能力的 SACC 细胞系 SACC-83 相比,高转移性 SACC 细胞系 SACC-LM 中 EMMPRIN 表达上调。用其抗体阻断 EMMPRIN 可显著降低 SACC-LM 细胞的黏附、MMP-2 和 MMP-9 的分泌以及体外侵袭活性(P<0.01)。与单独培养 SACC-LM 细胞相比,SACC-LM 细胞与成纤维细胞共培养可显著增加 MMP-2 和 MMP-9 的产生,并促进 SACC-LM 细胞的体外侵袭活性(P<0.01)。这些结果表明,EMMPRIN 通过刺激肿瘤和基质细胞中 MMP-2 和 MMP-9 的表达,可能在 SACC 的侵袭中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb09/3583551/c7cbd54b7cb2/OR-27-04-1123-g0.jpg

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