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永生化癌相关成纤维细胞促进前列腺癌的发生、增殖和侵袭。

Immortalized Cancer-associated Fibroblasts Promote Prostate Cancer Carcinogenesis, Proliferation and Invasion.

作者信息

Yu Shengqiang, Jiang Yingjuan, Wan Fengchun, Wu Jitao, Gao Zhenli, Liu Dongfu

机构信息

Department of Urology, the Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, P.R. China.

Yantai Maternal and Child Health Hospital, Yantai, P.R. China.

出版信息

Anticancer Res. 2017 Aug;37(8):4311-4318. doi: 10.21873/anticanres.11824.

Abstract

BACKGROUND

Cancer-associated fibroblasts (CAFs) are dominant components of the prostate cancer (PCa) stroma. However, the contrasting effects of CAFs and adjacent normal prostate fibroblasts (NPFs) are still poorly defined. The senescence of non-immortalized CAFs after subculture may limit the cell number and influence experimental results of in vitro studies. In this study, we immortalized CAFs to study their role in PCa carcinogenesis, proliferation, and invasion.

MATERIALS AND METHODS

We cultured and immortalized CAFs and NPFs, then compared their effect on epithelial malignant transformation by using in vitro co-culture, soft agar assay, and a mouse renal capsule xenograft model. We also compared their roles in PCa progression by using in vitro co-culture, cell viability assays, invasion assays, and a mouse xenograft model. For the mechanistic study, we screened a series of growth factors by using real-time polymerase chain reaction.

RESULTS

The CAFs and NPFs were successfully cultured, immortalized, and characterized. The CAFs were able to transform prostate epithelial cells into malignant cells, but NPFs were not. The CAFs were more active in promoting proliferation of and invasion by PCa cells, and in secreting higher levels of a series of growth factors.

CONCLUSION

The immortalized CAFs were more supportive of PCa carcinogenesis and progression. Targeting CAFs might be a potential option for PCa therapy. Immortalized CAFs and NPFs will also be valuable resources for future experimental exploration.

摘要

背景

癌症相关成纤维细胞(CAFs)是前列腺癌(PCa)基质的主要成分。然而,CAFs与相邻正常前列腺成纤维细胞(NPFs)的对比作用仍不清楚。传代培养后未永生化的CAFs衰老可能会限制细胞数量并影响体外研究的实验结果。在本研究中,我们使CAFs永生化以研究它们在PCa致癌、增殖和侵袭中的作用。

材料与方法

我们培养并使CAFs和NPFs永生化,然后通过体外共培养、软琼脂试验和小鼠肾包膜异种移植模型比较它们对上皮恶性转化的影响。我们还通过体外共培养、细胞活力测定、侵袭试验和小鼠异种移植模型比较它们在PCa进展中的作用。对于机制研究,我们通过实时聚合酶链反应筛选了一系列生长因子。

结果

CAFs和NPFs成功培养、永生化并进行了表征。CAFs能够将前列腺上皮细胞转化为恶性细胞,但NPFs不能。CAFs在促进PCa细胞增殖和侵袭以及分泌一系列更高水平的生长因子方面更活跃。

结论

永生化的CAFs更支持PCa的致癌作用和进展。靶向CAFs可能是PCa治疗的一个潜在选择。永生化的CAFs和NPFs也将是未来实验探索的宝贵资源。

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