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核受体共抑制因子(NCoR)是宫颈癌的一个预后良好的标志物。

Nuclear receptor corepressor (NCoR) is a positive prognosticator for cervical cancer.

机构信息

Department of Obstetrics and Gynaecology, Ludwig-Maximilians-University of Munich, Maistrasse 11, 80337, Munich, Germany.

Department of Pathology, LMU Munich, Thalkirchner Street 56, 80337, Munich, Germany.

出版信息

Arch Gynecol Obstet. 2021 Nov;304(5):1307-1314. doi: 10.1007/s00404-021-06053-3. Epub 2021 Apr 16.


DOI:10.1007/s00404-021-06053-3
PMID:33861372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8490237/
Abstract

PURPOSE: Enzymes with epigenetic functions play an essential part in development of cancer. However, the significance of epigenetic changes in cervical carcinoma as a prognostic factor has not been fully investigated. Nuclear receptor corepressor (NCoR) presents itself as a potentially important element for epigenetic modification and as a potential prognostic aspect in cervical cancer. METHODS: By immunohistochemical staining of 250 tumor samples, the expression strength of NCoR was measured and evaluated by immunoreactive score (IRS) in the nucleus and cytoplasm. RESULTS: A low expression of NCoR in our patients was a disadvantage in overall survival. Expression of NCoR was negatively correlated with viral oncoprotein E6, acetylated histone H3 acetyl K9 and FIGO status, and positively correlated to p53. CONCLUSIONS: Our study has identified epigenetic modification of tumor cells thus seems to be of relevance in cervical cancer as well for diagnosis, as a marker or as a potential therapeutic target in patients with advanced cervical carcinoma.

摘要

目的:具有表观遗传功能的酶在癌症的发展中起着至关重要的作用。然而,表观遗传变化在宫颈癌作为预后因素的意义尚未得到充分研究。核受体辅抑制因子(NCoR)作为表观遗传修饰的潜在重要因素和宫颈癌的潜在预后因素。

方法:通过对 250 个肿瘤样本的免疫组织化学染色,用免疫反应评分(IRS)测量细胞核和细胞质中 NCoR 的表达强度。

结果:我们的患者中 NCoR 的低表达在总生存中是不利的。NCoR 的表达与病毒癌蛋白 E6、乙酰化组蛋白 H3 乙酰 K9 和 FIGO 状态呈负相关,与 p53 呈正相关。

结论:我们的研究已经确定了肿瘤细胞的表观遗传修饰,因此在宫颈癌的诊断、作为标志物或作为晚期宫颈癌患者的潜在治疗靶点方面似乎具有相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/8490237/f5676c2e678b/404_2021_6053_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/8490237/bc066b3ca7e6/404_2021_6053_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/8490237/bbc77e4488a8/404_2021_6053_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/8490237/f5676c2e678b/404_2021_6053_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/8490237/bc066b3ca7e6/404_2021_6053_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/8490237/bbc77e4488a8/404_2021_6053_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/8490237/f5676c2e678b/404_2021_6053_Fig3_HTML.jpg

相似文献

[1]
Nuclear receptor corepressor (NCoR) is a positive prognosticator for cervical cancer.

Arch Gynecol Obstet. 2021-11

[2]
Histone H3 Acetyl K9 and Histone H3 Tri Methyl K4 as Prognostic Markers for Patients with Cervical Cancer.

Int J Mol Sci. 2017-2-23

[3]
Cyclooxygenase-2 transcription is regulated by human papillomavirus 16 E6 and E7 oncoproteins: evidence of a corepressor/coactivator exchange.

Cancer Res. 2007-4-15

[4]
Human papilloma virus early proteins E6 (HPV16/18-E6) and the cell cycle marker P16 (INK4a) are useful prognostic markers in uterine cervical carcinomas in Qassim Region--Saudi Arabia.

Pathol Oncol Res. 2015-1

[5]
Autoregulatory loop of nuclear corepressor 1 expression controls invasion, tumor growth, and metastasis.

Proc Natl Acad Sci U S A. 2016-1-19

[6]
Berberine alters epigenetic modifications, disrupts microtubule network, and modulates HPV-18 E6-E7 oncoproteins by targeting p53 in cervical cancer cell HeLa: a mechanistic study including molecular docking.

Eur J Pharmacol. 2014-10-18

[7]
Expression of estrogen receptor co-regulators NCoR and PELP1 in epithelial cells and myofibroblasts of colorectal carcinomas: cytoplasmic translocation of NCoR in epithelial cells correlates with better [corrected] prognosis.

Virchows Arch. 2009-1

[8]
The presence of human papillomavirus-16/-18 E6, p53, and Bcl-2 protein in cervicovaginal smears from patients with invasive cervical cancer.

Cancer Epidemiol Biomarkers Prev. 1996-5

[9]
Immunohistochemical Evaluation of E6/E7 HPV Oncoproteins Staining in Cervical Cancer.

Anticancer Res. 2016-6

[10]
HPV-mediated nuclear export of HP1γ drives cervical tumorigenesis by downregulation of p53.

Cell Death Differ. 2020-9

引用本文的文献

[1]
SPOP promotes cervical cancer progression by inducing the movement of PD-1 away from PD-L1 in spatial localization.

J Transl Med. 2022-8-30

[2]
Compatibility of ingredients of Danshen (Radix ) and Honghua () and their protective effects on cerebral ischemia-reperfusion injury in rats.

Exp Ther Med. 2021-8

本文引用的文献

[1]
Evolution of NCoR-1 and NCoR-2 corepressor alternative mRNA splicing in placental mammals.

BMC Res Notes. 2019-6-17

[2]
Different expression of GSK3β and pS9GSK3β depending on phenotype of cervical cancer: possible association of GSK3β with squamous cell carcinoma and pS9GSK3β with adenocarcinoma.

Obstet Gynecol Sci. 2019-5

[3]
Investigation of RIP140 and LCoR as independent markers for poor prognosis in cervical cancer.

Oncotarget. 2017-10-31

[4]
The involvement of E6, p53, p16, MDM2 and Gal-3 in the clinical outcome of patients with cervical cancer.

Oncol Lett. 2017-10

[5]
Histone H3 Acetyl K9 and Histone H3 Tri Methyl K4 as Prognostic Markers for Patients with Cervical Cancer.

Int J Mol Sci. 2017-2-23

[6]
Hedgehog inhibition enhances efficacy of radiation and cisplatin in orthotopic cervical cancer xenografts.

Br J Cancer. 2017-1-3

[7]
Immunohistochemical Evaluation of E6/E7 HPV Oncoproteins Staining in Cervical Cancer.

Anticancer Res. 2016-6

[8]
Nuclear receptor corepressor complexes in cancer: mechanism, function and regulation.

Am J Clin Exp Urol. 2014-10-2

[9]
Clinical implications of (epi)genetic changes in HPV-induced cervical precancerous lesions.

Nat Rev Cancer. 2014-6

[10]
Filling a gap in cervical cancer screening programmes.

Lancet Oncol. 2014-3

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