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宫颈肿瘤的分子特征分析。

Molecular profiling of cervical neoplasia.

作者信息

Martin Cara M, Astbury Katharine, O'Leary John J

机构信息

Department of Pathology, Coombe Women's Hospital, Dublin 8, Ireland.

出版信息

Expert Rev Mol Diagn. 2006 Mar;6(2):217-29. doi: 10.1586/14737159.6.2.217.

DOI:10.1586/14737159.6.2.217
PMID:16512781
Abstract

Cervical cancer, a potentially preventable disease, remains the second most common malignancy in women worldwide. Human papillomavirus is the single most important etiological agent in cervical cancer, contributing to neoplastic progression through the action of viral oncoproteins, mainly E6 and E7, which interfere with critical cell cycle pathways, p53 and retinoblastoma. However, evidence suggests that human papillomavirus infection alone is insufficient to induce malignant changes and that other host genetic variations are important in the development of cervical cancer. This article will discuss the latest molecular profiling techniques available and review the published literature relating to their role in the diagnosis and management of cervical dysplasia and cancer. It is hoped that these techniques will allow the detection of novel biomarkers at DNA, RNA, microRNA and protein levels, which may ultimately play a role in facilitating early disease diagnosis and in predicting response to therapies, thus allowing the development of personalized treatment strategies.

摘要

宫颈癌是一种潜在可预防的疾病,仍然是全球女性中第二常见的恶性肿瘤。人乳头瘤病毒是宫颈癌中唯一最重要的病因,通过病毒癌蛋白(主要是E6和E7)的作用导致肿瘤进展,这些蛋白干扰关键的细胞周期途径、p53和视网膜母细胞瘤。然而,有证据表明,仅人乳头瘤病毒感染不足以诱发恶性变化,其他宿主基因变异在宫颈癌的发生发展中也很重要。本文将讨论现有的最新分子分析技术,并回顾已发表的有关它们在宫颈发育异常和癌症诊断及管理中作用的文献。希望这些技术能够在DNA、RNA、微小RNA和蛋白质水平检测到新的生物标志物,这最终可能有助于早期疾病诊断和预测对治疗的反应,从而制定个性化的治疗策略。

相似文献

1
Molecular profiling of cervical neoplasia.宫颈肿瘤的分子特征分析。
Expert Rev Mol Diagn. 2006 Mar;6(2):217-29. doi: 10.1586/14737159.6.2.217.
2
Gene expression profiling in cervical cancer: identification of novel markers for disease diagnosis and therapy.宫颈癌中的基因表达谱分析:疾病诊断与治疗新标志物的鉴定
Methods Mol Biol. 2009;511:333-59. doi: 10.1007/978-1-59745-447-6_15.
3
HPV and cervical cancer: updates on an established relationship.人乳头瘤病毒与宫颈癌:既定关系的最新进展
Postgrad Med. 2008 Nov;120(4):7-13. doi: 10.3810/pgm.2008.11.1928.
4
Multiple biomarkers in molecular oncology. I. Molecular diagnostics applications in cervical cancer detection.分子肿瘤学中的多种生物标志物。I. 分子诊断在宫颈癌检测中的应用。
Expert Rev Mol Diagn. 2007 Mar;7(2):117-31. doi: 10.1586/14737159.7.2.117.
5
High human papillomavirus oncogene mRNA expression and not viral DNA load is associated with poor prognosis in cervical cancer patients.高危型人乳头瘤病毒癌基因mRNA表达而非病毒DNA载量与宫颈癌患者的预后不良相关。
Clin Cancer Res. 2007 Jan 1;13(1):132-8. doi: 10.1158/1078-0432.CCR-06-1568.
6
Gene discovery in cervical cancer : towards diagnostic and therapeutic biomarkers.宫颈癌中的基因发现:迈向诊断和治疗生物标志物
Mol Diagn Ther. 2007;11(5):277-90. doi: 10.1007/BF03256249.
7
Silencing of HPV 18 oncoproteins With RNA interference causes growth inhibition of cervical cancer cells.通过RNA干扰使HPV 18癌蛋白沉默可导致宫颈癌细胞生长受到抑制。
Reprod Sci. 2007 Jan;14(1):20-8. doi: 10.1177/1933719106298189.
8
Human papillomavirus E6/E7 mRNA testing as a predictive marker for cervical carcinoma.人乳头瘤病毒E6/E7信使核糖核酸检测作为宫颈癌的预测标志物
Expert Rev Mol Diagn. 2008 Jul;8(4):405-15. doi: 10.1586/14737159.8.4.405.
9
Antisense targeting human papillomavirus type 16 E6 and E7 genes contributes to apoptosis and senescence in SiHa cervical carcinoma cells.反义靶向人乳头瘤病毒16型E6和E7基因可促进SiHa宫颈癌细胞的凋亡和衰老。
Gynecol Oncol. 2007 Aug;106(2):299-304. doi: 10.1016/j.ygyno.2007.04.039. Epub 2007 Jun 21.
10
Role of proteomics in translational research in cervical cancer.蛋白质组学在宫颈癌转化研究中的作用。
Expert Rev Proteomics. 2006 Feb;3(1):21-36. doi: 10.1586/14789450.3.1.21.

引用本文的文献

1
[Over-expression of miR-519d alters gene expression profiles of cervical cancer SiHa cells].[miR-519d过表达改变宫颈癌SiHa细胞的基因表达谱]
Nan Fang Yi Ke Da Xue Xue Bao. 2018 Jul 30;38(7):794-799. doi: 10.3969/j.issn.1673-4254.2018.07.04.
2
Let-7g affects cell proliferation, migration and invasion in cervical squamous cell carcinomas via targeting collagen I.Let-7g通过靶向胶原蛋白I影响宫颈鳞状细胞癌的细胞增殖、迁移和侵袭。
Int J Clin Exp Pathol. 2018 Jul 1;11(7):3416-3425. eCollection 2018.
3
microRNA-214 suppresses the growth of cervical cancer cells by targeting EZH2.
微小RNA-214通过靶向EZH2抑制宫颈癌细胞的生长。
Oncol Lett. 2018 Nov;16(5):5679-5686. doi: 10.3892/ol.2018.9363. Epub 2018 Aug 24.
4
MicroRNA-10b inhibits proliferation, migration and invasion in cervical cancer cells via direct targeting of insulin-like growth factor-1 receptor.微小RNA-10b通过直接靶向胰岛素样生长因子-1受体抑制宫颈癌细胞的增殖、迁移和侵袭。
Oncol Lett. 2017 Jun;13(6):5009-5015. doi: 10.3892/ol.2017.6033. Epub 2017 Apr 13.
5
Amplification and up-regulation of MIR30D was associated with disease progression of cervical squamous cell carcinomas.MIR30D的扩增和上调与宫颈鳞状细胞癌的疾病进展相关。
BMC Cancer. 2017 Mar 29;17(1):230. doi: 10.1186/s12885-017-3201-0.
6
Novel epigenetic changes in CDKN2A are associated with progression of cervical intraepithelial neoplasia.CDKN2A基因的新型表观遗传变化与宫颈上皮内瘤变的进展相关。
Gynecol Oncol. 2016 Sep;142(3):566-73. doi: 10.1016/j.ygyno.2016.07.006. Epub 2016 Jul 9.
7
Simultaneous [18F]FDG-PET/MRI: Correlation of Apparent Diffusion Coefficient (ADC) and Standardized Uptake Value (SUV) in Primary and Recurrent Cervical Cancer.同步[18F]氟代脱氧葡萄糖正电子发射断层显像/磁共振成像:原发性和复发性宫颈癌中表观扩散系数(ADC)与标准化摄取值(SUV)的相关性
PLoS One. 2015 Nov 9;10(11):e0141684. doi: 10.1371/journal.pone.0141684. eCollection 2015.
8
The expression of Mcl-1 in human cervical cancer and its clinical significance.Mcl-1 在人宫颈癌中的表达及其临床意义。
Med Oncol. 2012 Sep;29(3):1985-91. doi: 10.1007/s12032-011-0005-y. Epub 2011 Jun 15.
9
Identification of miR-23a as a novel microRNA normalizer for relative quantification in human uterine cervical tissues.鉴定 miR-23a 作为一种新型 miRNA 内参用于人子宫颈组织相对定量。
Exp Mol Med. 2011 Jun 30;43(6):358-66. doi: 10.3858/emm.2011.43.6.039.
10
Distribution of CCND1 A870G polymorphism in patients with advanced uterine cervical carcinoma.CCND1 A870G 多态性在晚期子宫颈癌患者中的分布。
Pathol Oncol Res. 2011 Mar;17(1):133-7. doi: 10.1007/s12253-010-9293-3. Epub 2010 Aug 3.