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Expression of A disintegrin and metalloprotease 10 in pancreatic carcinoma.

机译:A整联蛋白和金属蛋白酶10在胰腺癌中的表达。

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摘要

The protease ADAM10 influences progression and metastasis of cancer cells and is overexpressed in various malignancies. Therefore, the aim of our study was to evaluate the expression and potential function of ADAM10 in the pathophysiology of pancreatic cancer (PDAC). ADAM10 expression in normal pancreatic (NP), chronic pancreatitis (CP), PDAC tissues, as well as PDAC cell lines was determined. To evaluate whether rhADAM10 or ADAM10 silencing influences cancer cell viability, MTT assay was used. Matrigel invasion and wound healing assays were performed to observe influence on invasion and migration. ADAM10 mRNA was expressed in all samples of NP, CP and PDAC tissue and cell lines. Western blotting and immunohistochemistry revealed stronger ADAM10 expression in PDAC than in NP. ADAM10 silencing or rhADAM10 had no effect on cell viability. ADAM10 silencing markedly reduced invasiveness and migration of cancer cells. These findings establish ADAM10 as a contributing factor in PDAC invasion and metastasis.
机译:蛋白酶ADAM10影响癌细胞的进展和转移,并在各种恶性肿瘤中过表达。因此,我们的研究目的是评估ADAM10在胰腺癌(PDAC)病理生理中的表达及其潜在功能。确定ADAM10在正常胰腺(NP),慢性胰腺炎(CP),PDAC组织以及PDAC细胞系中的表达。为了评估rhADAM10或ADAM10沉默是否影响癌细胞生存力,使用了MTT分析。进行基质胶侵袭和伤口愈合测定以观察对侵袭和迁移的影响。 ADAM10 mRNA在NP,CP和PDAC组织和细胞系的所有样品中都有表达。免疫印迹和免疫组织化学分析显示,PDAC中ADAM10表达高于NP。 ADAM10沉默或rhADAM10对细胞活力没有影响。 ADAM10沉默显着降低了癌细胞的侵袭性和迁移。这些发现将ADAM10确立为PDAC侵袭和转移的重要因素。

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