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单核细胞系细胞在前列腺癌细胞侵袭和组织因子表达中的作用。

Role of monocyte-lineage cells in prostate cancer cell invasion and tissue factor expression.

机构信息

Department of Pathology, The Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.

出版信息

Prostate. 2010 Nov 1;70(15):1672-82. doi: 10.1002/pros.21202.

Abstract

BACKGROUND

Tissue factor (TF) is a cell surface glycoprotein intricately related to blood coagulation and inflammation. This study was performed to investigate the role of monocyte-lineage cells in prostate cancer cell TF expression and cell invasion.

METHODS

Prostate cancer cell invasion was tested with and without added peripheral blood monocytes or human monocyte-lineage cell lines. TF neutralizing antibodies were used to determine the TF requirement for prostate cancer cell invasion activity. Immunohistochemistry was performed to identify prostate tissue CD68 positive monocyte-derived cells and prostate epithelial TF expression.

RESULTS

Co-culture of PC-3, DU145, and LNCaP cells with isolated human monocytes significantly stimulated prostate cancer cell invasion activity. TF expression was greater in highly invasive prostate cancer cells and was induced in PC-3, DU145, and LNCaP cells by co-culture with U-937 cells, but not with THP-1 cells. TF neutralizing antibodies inhibited PC-3 cell invasion in co-cultures with monocyte-lineage U-937 or THP-1 cells. Prostate cancer tissues contained more CD68 positive cells in the stroma and epithelium (145 ± 53/mm(2)) than benign prostate (108 ± 31/mm(2)). Samples from advanced stage prostate cancer tended to contain more CD68 positive cells when compared with lower stage lesions. Prostatic adenocarcinoma demonstrated significantly increased TF expression compared with benign prostatic epithelium.

CONCLUSIONS

This study shows that co-culture with monocyte-lineage cells induced prostate cancer cell invasion activity. PC-3 invasion and TF expression was induced in co-culture with U-937 cells and partially inhibited with TF neutralizing antibodies.

摘要

背景

组织因子(TF)是一种细胞表面糖蛋白,与血液凝固和炎症密切相关。本研究旨在探讨单核细胞系在前列腺癌细胞 TF 表达和细胞侵袭中的作用。

方法

检测有无外周血单核细胞或人单核细胞系加入时前列腺癌细胞的侵袭情况。用 TF 中和抗体确定 TF 是否是前列腺癌细胞侵袭活性所必需的。用免疫组化鉴定前列腺组织 CD68 阳性单核细胞衍生细胞和前列腺上皮 TF 表达。

结果

PC-3、DU145 和 LNCaP 细胞与分离的人单核细胞共培养显著刺激前列腺癌细胞侵袭活性。高侵袭性前列腺癌细胞 TF 表达增加,与 U-937 细胞共培养可诱导 PC-3、DU145 和 LNCaP 细胞 TF 表达,但与 THP-1 细胞共培养则不能。TF 中和抗体可抑制与单核细胞系 U-937 或 THP-1 细胞共培养的 PC-3 细胞的侵袭。前列腺癌组织间质和上皮中 CD68 阳性细胞(145±53/mm²)多于良性前列腺组织(108±31/mm²)。与低分期病变相比,晚期前列腺癌样本中 CD68 阳性细胞更多。前列腺腺癌与良性前列腺上皮相比 TF 表达显著增加。

结论

本研究表明,与单核细胞系共培养诱导前列腺癌细胞侵袭活性。与 U-937 细胞共培养可诱导 PC-3 侵袭和 TF 表达,并部分被 TF 中和抗体抑制。

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