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雄激素受体和骨形成蛋白聚糖基因表达预测转移性前列腺癌的预后

Androgen receptor and osteoglycin gene expression predicting prognosis of metastatic prostate cancer.

作者信息

Kameda Tomohiro, Sugihara Toru, Obinata Daisuke, Oshima Masashi, Yamada Yuta, Kimura Naoki, Takayama Kenichi, Inoue Satoshi, Takahashi Satoru, Fujimura Tetsuya

机构信息

Department of Urology, Jichi Medical University, 3311-1 Yakushiji Shimotsuke, Tochigi, 329-0498, Japan.

Department of Urology, Nihon University School of Medicine, Tokyo, Japan.

出版信息

Sci Rep. 2024 Dec 28;14(1):30654. doi: 10.1038/s41598-024-74443-z.

DOI:10.1038/s41598-024-74443-z
PMID:39730360
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11680600/
Abstract

This study aimed to identify the predictive factors associated with the oncological outcomes of metastatic hormone-sensitive prostate cancer-related genes. A nomogram for predicting prostate cancer-specific survival (CSS) was constructed based on biopsy samples obtained from 103 patients with metastatic hormone-sensitive prostate cancer. We analyzed the association between clinical data and mRNA expression levels. The nomogram was externally validated in another cohort (n = 50) by using a concordance index. Based on the cutoff value, determined by a receiver operating characteristic analysis, longer CSS was observed in the high osteoglycin and androgen receptor expression level groups (> 1.133 and > 0.00; median CSS, 85.3 vs. 52.7 months, p = 0.045, and 69.1 vs. 32.1 months, p = 0.034, respectively), compared with that of the low expression level groups. The nomogram predicting CSS included hemoglobin (≥ 13.7 g/dL or < 13.7 g/dL), serum albumin (≥ 3.1 g/dL or < 3.1 g/dL), serum lactate dehydrogenase (≥ 222 IU/L or < 222 IU/L), total Japan Cancer of the Prostate Risk Assessment score, androgen receptor expression level, and osteoglycin expression level. The concordance indices for the internal and external validations were 0.664 and 0.798, respectively. In this study, a nomogram that integrated the expression levels of androgen receptors and osteoglycin to predict CSS in metastatic hormone-sensitive prostate cancer was established.

摘要

本研究旨在确定与转移性激素敏感性前列腺癌相关基因的肿瘤学结局相关的预测因素。基于从103例转移性激素敏感性前列腺癌患者获得的活检样本构建了预测前列腺癌特异性生存(CSS)的列线图。我们分析了临床数据与mRNA表达水平之间的关联。通过一致性指数在另一个队列(n = 50)中对列线图进行了外部验证。根据受试者工作特征分析确定的临界值,与低表达水平组相比,在高骨甘蛋白和雄激素受体表达水平组(> 1.133和> 0.00;CSS中位数分别为85.3个月对52.7个月,p = 0.045,以及69.1个月对32.1个月,p = 0.034)中观察到更长的CSS。预测CSS的列线图包括血红蛋白(≥13.7 g/dL或<13.7 g/dL)、血清白蛋白(≥3.1 g/dL或<3.1 g/dL)、血清乳酸脱氢酶(≥222 IU/L或<222 IU/L)、日本前列腺癌总风险评估评分、雄激素受体表达水平和骨甘蛋白表达水平。内部验证和外部验证的一致性指数分别为0.664和0.798。在本研究中,建立了一个整合雄激素受体和骨甘蛋白表达水平以预测转移性激素敏感性前列腺癌CSS的列线图。

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本文引用的文献

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Osteoglycin (OGN) promotes tumorigenesis of pancreatic cancer cell via targeting ID4.骨粘连蛋白(OGN)通过靶向 ID4 促进胰腺癌的肿瘤发生。
Tissue Cell. 2022 Oct;78:101867. doi: 10.1016/j.tice.2022.101867. Epub 2022 Jul 16.
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Identification of key genes associated with polycystic ovary syndrome (PCOS) and ovarian cancer using an integrated bioinformatics analysis.利用综合生物信息学分析鉴定与多囊卵巢综合征(PCOS)和卵巢癌相关的关键基因。
J Ovarian Res. 2022 Feb 28;15(1):30. doi: 10.1186/s13048-022-00962-w.
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ECRG4 Represses Cell Proliferation and Invasiveness via NFIC/OGN/NF-κB Signaling Pathway in Bladder Cancer.
ECRG4通过NFIC/OGN/NF-κB信号通路抑制膀胱癌的细胞增殖和侵袭能力。
Front Genet. 2020 Aug 14;11:846. doi: 10.3389/fgene.2020.00846. eCollection 2020.
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Osteoglycin (OGN) Inhibits Cell Proliferation and Invasiveness in Breast Cancer via PI3K/Akt/mTOR Signaling Pathway.骨甘蛋白(OGN)通过PI3K/Akt/mTOR信号通路抑制乳腺癌细胞的增殖和侵袭能力。
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Abiraterone acetate plus prednisone in patients with newly diagnosed high-risk metastatic castration-sensitive prostate cancer (LATITUDE): final overall survival analysis of a randomised, double-blind, phase 3 trial.醋酸阿比特龙联合泼尼松治疗新诊断的高危转移性去势敏感性前列腺癌(LATITUDE):一项随机、双盲、III 期临床试验的最终总生存分析。
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Osteoglycin (OGN) reverses epithelial to mesenchymal transition and invasiveness in colorectal cancer via EGFR/Akt pathway.骨连接蛋白(OGN)通过 EGFR/Akt 通路逆转结直肠癌细胞的上皮间质转化和侵袭。
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Chemohormonal Therapy in Metastatic Hormone-Sensitive Prostate Cancer: Long-Term Survival Analysis of the Randomized Phase III E3805 CHAARTED Trial.转移性激素敏感前列腺癌的化学生物治疗:随机 III 期 E3805 CHAARTED 试验的长期生存分析。
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