• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

复发性前列腺癌挽救性放射治疗后FOXA1染色水平与生化复发之间关联的研究。

An Examination of the Association between FOXA1 Staining Level and Biochemical Recurrence following Salvage Radiation Therapy for Recurrent Prostate Cancer.

作者信息

Heckman Michael G, Robinson Jessica L, Tzou Katherine S, Parker Alexander S, Wu Kevin J, Hilton Tracy W, Howat William J, Miller Jodi L, Kreinest Pamela A, Pisansky Thomas M, Schild Steven E, Peterson Jennifer L, Vallow Laura A, Carroll Jason S, Buskirk Steven J

机构信息

Department of Health Sciences Research, Mayo Clinic, Jacksonville, Florida, United States of America.

Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom.

出版信息

PLoS One. 2016 Mar 17;11(3):e0151785. doi: 10.1371/journal.pone.0151785. eCollection 2016.

DOI:10.1371/journal.pone.0151785
PMID:26986977
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4795739/
Abstract

BACKGROUND

Standardly collected clinical and pathological patient information has demonstrated only moderate ability to predict risk of biochemical recurrence (BCR) of prostate cancer in men undergoing salvage radiation therapy (SRT) for a rising PSA after radical prostatectomy (RP). Although elevated FOXA1 staining has been associated with poor patient outcomes following RP, it has not been studied in the specific setting of SRT after RP. The aim of this study was to evaluate the association between FOXA1 staining level and BCR after SRT for recurrent prostate cancer.

METHODS

A total of 141 men who underwent SRT at our institution were included. FOXA1 staining levels in primary tumor samples were detected using immunohistochemistry. FOXA1 staining percentage and intensity were measured and multiplied together to obtain a FOXA1 H-score (range 0-12) which was our primary staining measure. P-values ≤ 0.0056 were considered as statistically significant after applying a Bonferroni correction for multiple comparisons.

RESULTS

There was not a significant association between FOXA1 H-score and risk of BCR when considering H-score as an ordinal variable or as a categorical variable (all P ≥ 0.090). Similarly, no significant associations with BCR were observed for FOXA1 staining percentage or staining intensity (all P ≥ 0.14).

CONCLUSIONS

FOXA1 staining level does not appear to have a major impact on risk of BCR after SRT.

摘要

背景

对于根治性前列腺切除术(RP)后前列腺特异抗原(PSA)升高而接受挽救性放射治疗(SRT)的男性患者,标准收集的临床和病理患者信息显示,其预测前列腺癌生化复发(BCR)风险的能力仅为中等。尽管FOXA1染色升高与RP后患者不良预后相关,但在RP后SRT的特定情况下尚未进行研究。本研究的目的是评估复发性前列腺癌SRT后FOXA1染色水平与BCR之间的关联。

方法

纳入了在我们机构接受SRT的141名男性。使用免疫组织化学检测原发肿瘤样本中的FOXA1染色水平。测量FOXA1染色百分比和强度并将两者相乘,以获得FOXA1 H评分(范围0 - 12),这是我们的主要染色测量指标。在应用Bonferroni校正进行多重比较后,P值≤0.0056被认为具有统计学意义。

结果

将H评分视为有序变量或分类变量时,FOXA1 H评分与BCR风险之间均无显著关联(所有P≥0.090)。同样,FOXA1染色百分比或染色强度与BCR也无显著关联(所有P≥0.14)。

结论

FOXA1染色水平似乎对SRT后BCR风险没有重大影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c4b/4795739/2410bf510751/pone.0151785.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c4b/4795739/a1300992d512/pone.0151785.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c4b/4795739/2410bf510751/pone.0151785.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c4b/4795739/a1300992d512/pone.0151785.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c4b/4795739/2410bf510751/pone.0151785.g002.jpg

相似文献

1
An Examination of the Association between FOXA1 Staining Level and Biochemical Recurrence following Salvage Radiation Therapy for Recurrent Prostate Cancer.复发性前列腺癌挽救性放射治疗后FOXA1染色水平与生化复发之间关联的研究。
PLoS One. 2016 Mar 17;11(3):e0151785. doi: 10.1371/journal.pone.0151785. eCollection 2016.
2
GATA2 expression and biochemical recurrence following salvage radiation therapy for relapsing prostate cancer.挽救性放射治疗复发性前列腺癌后GATA2表达与生化复发
Br J Radiol. 2017 Jul;90(1075):20170174. doi: 10.1259/bjr.20170174. Epub 2017 Jun 16.
3
Salvage radiotherapy for biochemical recurrence after radical prostatectomy: does the outcome depend on the prostate cancer characteristics?根治性前列腺切除术后生化复发的挽救性放疗:疗效是否取决于前列腺癌特征?
Int Braz J Urol. 2019 Mar-Apr;45(2):237-245. doi: 10.1590/S1677-5538.IBJU.2018.0039.
4
Evaluation of MDM2, p16, and p53 staining levels as biomarkers of biochemical recurrence following salvage radiation therapy for recurrent prostate cancer.评估 MDM2、p16 和 p53 染色水平作为挽救性放疗后复发性前列腺癌生化复发的生物标志物。
Prostate. 2012 Dec 1;72(16):1757-66. doi: 10.1002/pros.22528. Epub 2012 Apr 18.
5
Treatment Outcomes from Ga-PSMA PET/CT-Informed Salvage Radiation Treatment in Men with Rising PSA After Radical Prostatectomy: Prognostic Value of a Negative PSMA PET.根治性前列腺切除术后 PSA 升高男性患者接受 Ga-PSMA PET/CT 引导下挽救性放射治疗的疗效:PSMA PET 阴性的预后价值
J Nucl Med. 2017 Dec;58(12):1972-1976. doi: 10.2967/jnumed.117.196683. Epub 2017 Jul 26.
6
Salvage radiation therapy for prostate cancer patients after prostatectomy.前列腺切除术后的前列腺癌患者的挽救性放射治疗。
Jpn J Clin Oncol. 2019 Mar 1;49(3):281-286. doi: 10.1093/jjco/hyy195.
7
Assessing the Optimal Timing for Early Salvage Radiation Therapy in Patients with Prostate-specific Antigen Rise After Radical Prostatectomy.评估前列腺癌根治术后前列腺特异性抗原升高患者早期挽救性放射治疗的最佳时机
Eur Urol. 2016 Apr;69(4):728-733. doi: 10.1016/j.eururo.2015.10.009. Epub 2015 Oct 21.
8
Importance of the site of positive surgical margin in salvage external beam radiation therapy for biochemical recurrence of prostate cancer after radical prostatectomy.根治性前列腺切除术后生化复发的前列腺癌挽救性外照射放疗中阳性切缘部位的重要性。
Cancer Med. 2018 May;7(5):1723-1730. doi: 10.1002/cam4.1408. Epub 2018 Mar 23.
9
Impact of Biochemical Failure After Salvage Radiation Therapy on Prostate Cancer-specific Mortality: Competition Between Age and Time to Biochemical Failure.挽救性放疗后生化失败对前列腺癌特异性死亡率的影响:年龄与生化失败时间之间的竞争。
Eur Urol Oncol. 2018 Sep;1(4):276-282. doi: 10.1016/j.euo.2018.04.014. Epub 2018 Sep 28.
10
Salvage radiotherapy in prostate cancer patients with biochemical relapse after radical prostatectomy : Prolongation of prostate-specific antigen doubling time in patients with subsequent biochemical progression.根治性前列腺切除术后生化复发的前列腺癌患者的挽救性放疗:随后生化进展患者的前列腺特异性抗原倍增时间延长。
Strahlenther Onkol. 2018 Apr;194(4):325-332. doi: 10.1007/s00066-017-1247-1. Epub 2017 Dec 18.

引用本文的文献

1
FOXA1 expression and its association with mucin expression and KRAS mutation in ovarian mucinous tumors: implications for tumor progression and differentiation.FOXA1在卵巢黏液性肿瘤中的表达及其与黏蛋白表达和KRAS突变的关系:对肿瘤进展和分化的影响
Virchows Arch. 2025 Jan 17. doi: 10.1007/s00428-025-04025-5.
2
Gene expression profiling of breast cancer cell lines treated with proton and electron radiations.质子和电子辐射处理的乳腺癌细胞系的基因表达谱分析。
Br J Radiol. 2018 Sep;91(1089):20170934. doi: 10.1259/bjr.20170934. Epub 2018 Jul 5.

本文引用的文献

1
Integrative analysis identifies targetable CREB1/FoxA1 transcriptional co-regulation as a predictor of prostate cancer recurrence.综合分析确定可靶向的CREB1/FoxA1转录共调控作为前列腺癌复发的一个预测指标。
Nucleic Acids Res. 2017 Jun 20;45(11):6993. doi: 10.1093/nar/gkx282.
2
Proposed prognostic scoring system evaluating risk factors for biochemical recurrence of prostate cancer after salvage radiation therapy.
BJU Int. 2016 Aug;118(2):236-42. doi: 10.1111/bju.13229. Epub 2015 Aug 22.
3
A comprehensive assessment of the prognostic utility of the Stephenson nomogram for salvage radiation therapy postprostatectomy.对斯蒂芬森列线图在前列腺切除术后挽救性放射治疗中的预后效用进行全面评估。
Pract Radiat Oncol. 2014 Nov-Dec;4(6):422-9. doi: 10.1016/j.prro.2014.02.003. Epub 2014 Mar 27.
4
Elevated levels of FOXA1 facilitate androgen receptor chromatin binding resulting in a CRPC-like phenotype.FOXA1 水平升高可促进雄激素受体染色质结合,导致类似 CRPC 的表型。
Oncogene. 2014 Dec 11;33(50):5666-74. doi: 10.1038/onc.2013.508. Epub 2013 Dec 2.
5
Gleason pattern 5 is the strongest pathologic predictor of recurrence, metastasis, and prostate cancer-specific death in patients receiving salvage radiation therapy following radical prostatectomy.格里森 5 型是接受根治性前列腺切除术后挽救性放射治疗的患者复发、转移和前列腺癌特异性死亡的最强病理预测因子。
Cancer. 2013 Sep 15;119(18):3287-94. doi: 10.1002/cncr.28215. Epub 2013 Jul 2.
6
Androgen receptor-independent function of FoxA1 in prostate cancer metastasis.FoxA1 在前列腺癌转移中的雄激素受体非依赖性功能。
Cancer Res. 2013 Jun 15;73(12):3725-36. doi: 10.1158/0008-5472.CAN-12-3468. Epub 2013 Mar 28.
7
FOXA1 promotes tumor progression in prostate cancer via the insulin-like growth factor binding protein 3 pathway.FOXA1 通过胰岛素样生长因子结合蛋白 3 途径促进前列腺癌的肿瘤进展。
PLoS One. 2012;7(8):e42456. doi: 10.1371/journal.pone.0042456. Epub 2012 Aug 3.
8
FoxA1 is a key mediator of hormonal response in breast and prostate cancer.FoxA1 是乳腺癌和前列腺癌中激素反应的关键介质。
Front Endocrinol (Lausanne). 2012 May 18;3:68. doi: 10.3389/fendo.2012.00068. eCollection 2012.
9
FOXA1 promotes tumor progression in prostate cancer and represents a novel hallmark of castration-resistant prostate cancer.FOXA1 促进前列腺癌的肿瘤进展,是去势抵抗性前列腺癌的一个新标志。
Am J Pathol. 2012 Feb;180(2):848-61. doi: 10.1016/j.ajpath.2011.10.021. Epub 2011 Dec 2.
10
Dual role of FoxA1 in androgen receptor binding to chromatin, androgen signalling and prostate cancer.FoxA1 在雄激素受体与染色质结合、雄激素信号传导和前列腺癌中的双重作用。
EMBO J. 2011 Sep 13;30(19):3962-76. doi: 10.1038/emboj.2011.328.