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Hippo 信号通路效应物 YAP1 的上调与前列腺癌早期生化复发相关。

Up regulation of the Hippo signalling effector YAP1 is linked to early biochemical recurrence in prostate cancers.

机构信息

Institute of Pathology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.

Institute of Pathology, Klinikum Fürth, Fürth, Germany.

出版信息

Sci Rep. 2020 Jun 2;10(1):8916. doi: 10.1038/s41598-020-65772-w.

DOI:10.1038/s41598-020-65772-w
PMID:32488048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7265544/
Abstract

The transcriptional coactivator YAP1 controls the balance between cell proliferation and apoptosis. YAP1 overexpression is linked to poor prognosis in many cancer types, yet its role in prostate cancer is unknown. Here, we applied YAP1 immunohistochemistry to a tissue microarray containing 17,747 clinical prostate cancer specimens. Cytoplasmic and nuclear YAP1 staining was seen in 81% and 63% of tumours. For both cytoplasmic and nuclear YAP1 staining, high levels were associated with advanced tumour stage, classical and quantitative Gleason grade, positive nodal stage, positive surgical margin, high KI67 labelling index, and early biochemical recurrence (p < 0.0001 each). The prognostic role of YAP1 staining was independent of established prognostic features in multivariate models (p < 0.001). Comparison with previously studied molecular markers identified associations between high YAP1 staining, TMPRSS2:ERG fusion (p < 0.0001), high androgen receptor (AR) expression (p < 0.0001), high Ki67 labelling index (p < 0.0001), and PTEN and 8p deletions (p < 0.0001 each). In conclusion, high YAP1 protein expression is an independent predictor of unfavourable disease course in prostate cancer. That cytoplasmic and nuclear YAP1 staining is equally linked to phenotype and prognosis fits well to a model where YAP1 activation during tumour progression includes up regulation, cytoplasmic accumulation and subsequent translocation to the nucleus.

摘要

转录共激活因子 YAP1 控制细胞增殖和凋亡之间的平衡。YAP1 过表达与许多癌症类型的预后不良有关,但它在前列腺癌中的作用尚不清楚。在这里,我们应用 YAP1 免疫组织化学方法对包含 17747 例临床前列腺癌标本的组织微阵列进行了分析。在 81%和 63%的肿瘤中观察到细胞质和核 YAP1 染色。对于细胞质和核 YAP1 染色,高水平与肿瘤晚期、经典和定量 Gleason 分级、阳性淋巴结分期、阳性手术切缘、高 Ki67 标记指数和早期生化复发相关(p<0.0001 各)。在多变量模型中,YAP1 染色的预后作用独立于既定的预后特征(p<0.001)。与以前研究的分子标志物的比较确定了高 YAP1 染色与 TMPRSS2:ERG 融合(p<0.0001)、高雄激素受体(AR)表达(p<0.0001)、高 Ki67 标记指数(p<0.0001)和 PTEN 和 8p 缺失(p<0.0001 各)之间的关联。总之,高 YAP1 蛋白表达是前列腺癌不良疾病过程的独立预测因子。细胞质和核 YAP1 染色与表型和预后同样相关,这与肿瘤进展过程中 YAP1 激活包括上调、细胞质积累和随后易位到细胞核的模型非常吻合。

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本文引用的文献

1
The Hippo Signaling Pathway in Development and Disease.Hippo 信号通路在发育和疾病中的作用。
Dev Cell. 2019 Aug 5;50(3):264-282. doi: 10.1016/j.devcel.2019.06.003.
2
Yes-Associated Protein 1 as a Novel Prognostic Biomarker for Gastrointestinal Cancer: A Meta-Analysis.Yes 相关蛋白 1 作为一种新型的胃肠道癌症预后生物标志物:一项荟萃分析。
Biomed Res Int. 2018 Nov 14;2018:4039173. doi: 10.1155/2018/4039173. eCollection 2018.
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LMO3 promotes hepatocellular carcinoma invasion, metastasis and anoikis inhibition by directly interacting with LATS1 and suppressing Hippo signaling.
Am J Pathol. 2024 Mar;194(3):324-334. doi: 10.1016/j.ajpath.2023.12.003. Epub 2023 Dec 15.
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YAP1 inhibits RSL3-induced castration-resistant prostate cancer cell ferroptosis by driving glutamine uptake and metabolism to GSH.YAP1 通过驱动谷氨酰胺摄取和代谢为 GSH 来抑制 RSL3 诱导的去势抵抗性前列腺癌细胞铁死亡。
Mol Cell Biochem. 2024 Sep;479(9):2415-2427. doi: 10.1007/s11010-023-04847-4. Epub 2023 Sep 29.
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Yes-associated protein-1 overexpression in ocular surface squamous neoplasia; a potential diagnostic marker and therapeutic target.Yes相关蛋白-1在眼表鳞状上皮肿瘤中的过表达;一种潜在的诊断标志物和治疗靶点。
Front Oncol. 2023 Jul 5;13:1213426. doi: 10.3389/fonc.2023.1213426. eCollection 2023.
6
YAP1 and WWTR1 expression inversely correlates with neuroendocrine markers in Merkel cell carcinoma.YAP1 和 WWTR1 的表达与 Merkel 细胞癌中的神经内分泌标志物呈负相关。
J Clin Invest. 2023 Mar 1;133(5):e157171. doi: 10.1172/JCI157171.
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Curr Oncol. 2023 Jan 10;30(1):981-999. doi: 10.3390/curroncol30010075.
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Analyses of Transcriptomics Cell Signalling for Pre-Screening Applications in the Integrated Approach for Testing and Assessment of Non-Genotoxic Carcinogens.转录组细胞信号分析在非遗传毒性致癌物综合测试和评估方法中的预筛选应用。
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LMO3 通过与 LATS1 直接相互作用并抑制 Hippo 信号通路促进肝细胞癌侵袭、转移和抗失巢凋亡。
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Deletion lengthening at chromosomes 6q and 16q targets multiple tumor suppressor genes and is associated with an increasingly poor prognosis in prostate cancer.6号染色体长臂和16号染色体长臂的缺失延长靶向多个肿瘤抑制基因,并与前列腺癌预后越来越差相关。
Oncotarget. 2017 Nov 11;8(65):108923-108935. doi: 10.18632/oncotarget.22408. eCollection 2017 Dec 12.
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The correlation between poor prognosis and increased yes-associated protein 1 expression in keratin 19 expressing hepatocellular carcinomas and cholangiocarcinomas.在表达角蛋白19的肝细胞癌和胆管癌中,预后不良与Yes相关蛋白1表达增加之间的相关性。
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