Suppr超能文献

NFATc1在前列腺癌进展中的作用:环孢素A和他克莫司抑制细胞增殖、迁移和侵袭。

The role of NFATc1 in prostate cancer progression: cyclosporine A and tacrolimus inhibit cell proliferation, migration, and invasion.

作者信息

Kawahara Takashi, Kashiwagi Eiji, Ide Hiroki, Li Yi, Zheng Yichun, Ishiguro Hitoshi, Miyamoto Hiroshi

机构信息

Departments of Pathology and Urology, Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, New York.

出版信息

Prostate. 2015 May;75(6):573-84. doi: 10.1002/pros.22937. Epub 2015 Jan 28.

Abstract

BACKGROUND

The functional role of nuclear factor of activated T-cells (NFAT), a well-characterized regulator of the immune response, in prostate cancer progression remains largely unknown. We aim to investigate biological significance of NFATc1, a NFAT isoform shown to function as an oncogene in a sarcoma model, in human prostate cancer.

METHODS

We first determined the expression levels of NFAT in prostate cell lines and tissue specimens. We then assessed the effects of NFAT inhibition via NFATc1-small interfering RNA (siRNA) as well as immunosuppressants including cyclosporine A (CsA) and tacrolimus (FK506) on prostate cancer cell proliferation, apoptosis, migration, and invasion in vitro and in vivo.

RESULTS

Immunohistochemistry revealed that the expression levels of NFATc1 were significantly elevated in prostatic carcinomas, compared with non-neoplastic prostate or high-grade prostatic intraepithelial neoplasia tissues, and in high-grade (Gleason scores ≥7) tumors. NFATc1 positivity in carcinomas, as an independent prognosticator, also correlated with the risk of biochemical recurrence after radical prostatectomy. In prostate cancer cell lines, CsA and FK506 inhibited NFATc1 expression and its nuclear translocation, NFAT transcriptional activity, and the expression of c-myc, a downstream target of NFAT. NFAT silencing or treatment with these NFAT inhibitors resulted in decreases in cell viability/colony formation and cell migration/invasion, as well as increases in apoptosis, in androgen receptor (AR)-negative, AR-positive/androgen-sensitive, and AR-positive/castration-resistant lines. No significant additional inhibition in the growth of NFAT-siRNA cells by CsA and FK506 was seen, whereas these agents, especially FK506, further inhibited their invasion. In xenograft-bearing mice, CsA and FK506 significantly retarded tumor growth.

CONCLUSIONS

Our results suggest that NFATc1 plays an important role in prostate cancer outgrowth. Thus, NFATc1 inactivation, especially using CsA and FK506, has the potential of being a therapeutic approach for not only hormone-naïve but also castration-resistant prostate cancers.

摘要

背景

活化T细胞核因子(NFAT)是一种已被充分表征的免疫反应调节因子,其在前列腺癌进展中的功能作用仍 largely未知。我们旨在研究NFATc1(一种在肉瘤模型中显示具有癌基因功能的NFAT亚型)在人类前列腺癌中的生物学意义。

方法

我们首先测定了前列腺细胞系和组织标本中NFAT的表达水平。然后,我们评估了通过NFATc1小干扰RNA(siRNA)以及免疫抑制剂(包括环孢素A(CsA)和他克莫司(FK506))抑制NFAT对前列腺癌细胞在体外和体内的增殖、凋亡、迁移和侵袭的影响。

结果

免疫组织化学显示,与非肿瘤性前列腺组织或高级别前列腺上皮内瘤变组织以及高级别(Gleason评分≥7)肿瘤相比,前列腺癌中NFATc1的表达水平显著升高。癌组织中NFATc1阳性作为独立的预后指标,也与根治性前列腺切除术后生化复发的风险相关。在前列腺癌细胞系中,CsA和FK506抑制NFATc1表达及其核转位、NFAT转录活性以及NFAT下游靶点c-myc的表达。NFAT沉默或用这些NFAT抑制剂处理导致雄激素受体(AR)阴性、AR阳性/雄激素敏感和AR阳性/去势抵抗细胞系的细胞活力/集落形成以及细胞迁移/侵袭减少,同时凋亡增加。未观察到CsA和FK506对NFAT-siRNA细胞生长有显著的额外抑制作用,而这些药物,尤其是FK506,进一步抑制了它们的侵袭。在荷瘤小鼠中,CsA和FK506显著延缓了肿瘤生长。

结论

我们的结果表明NFATc1在前列腺癌生长中起重要作用。因此,NFATc1失活,尤其是使用CsA和FK506,不仅对激素初治的前列腺癌,而且对去势抵抗性前列腺癌都有可能成为一种治疗方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验