• 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

黑色素瘤患者外周血循环肿瘤细胞标志物与疾病复发和进展相关。

Markers of circulating tumour cells in the peripheral blood of patients with melanoma correlate with disease recurrence and progression.

机构信息

School of Medical Sciences, Edith Cowan University, Perth, WA, Australia.

出版信息

Br J Dermatol. 2013 Jan;168(1):85-92. doi: 10.1111/bjd.12057. Epub 2012 Nov 15.

DOI:10.1111/bjd.12057
PMID:23013138
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3538032/
Abstract

BACKGROUND

Multimarker quantitative real-time polymerase chain reaction (qRT-PCR) represents an effective method for detecting circulating tumour cells in the peripheral blood of patients with melanoma.

OBJECTIVES

To investigate whether the phenotype of circulating melanoma cells represents a useful indicator of disease stage, recurrence and treatment efficacy.

METHODS

Peripheral blood was collected from 230 patients with melanoma and 152 healthy controls over a period of 3years and 9months. Clinical data and blood samples were collected from patients with primary melanoma (early stages, 0-II, n=154) and metastatic melanoma (late stages, III-IV, n=76). Each specimen was examined by qRT-PCR analysis for the expression of five markers: MLANA, ABCB5, TGFβ2, PAX3d and MCAM.

RESULTS

In total, 212 of the patients with melanoma (92%) expressed markers in their peripheral blood. Two markers, MLANA and ABCB5, had the greatest prognostic value, and were identified as statistically significant among patients who experienced disease recurrence within our study period, being expressed in 45% (MLANA) and 49% (ABCB5) of patients with recurrence (P=0·001 and P=0·031, respectively). For patients administered nonsurgical treatments, MCAM expression correlated with poor treatment outcome.

CONCLUSIONS

Circulating tumour cells were detectable at all stages of disease and long after surgical treatment, even when patients were considered disease free. Specifically, expression of ABCB5 and MLANA had significant prognostic value in inferring disease recurrence, while MCAM expression was associated with poor patient outcome after treatment, confirming multimarker qRT-PCR as a potential technique for monitoring disease status.

摘要

背景

多标志物实时定量聚合酶链反应(qRT-PCR)是一种检测黑色素瘤患者外周血循环肿瘤细胞的有效方法。

目的

探讨循环黑素瘤细胞的表型是否代表疾病分期、复发和治疗效果的有用指标。

方法

在 3 年 9 个月的时间里,采集了 230 名黑色素瘤患者和 152 名健康对照者的外周血。采集了原发性黑色素瘤(早期,0-II 期,n=154)和转移性黑色素瘤(晚期,III-IV 期,n=76)患者的临床数据和血液样本。通过 qRT-PCR 分析,对 5 种标志物(MLANA、ABCB5、TGFβ2、PAX3d 和 MCAM)在每个标本中的表达进行了检测。

结果

共有 212 名黑色素瘤患者(92%)在其外周血中表达了标志物。两种标志物 MLANA 和 ABCB5 具有最大的预后价值,在本研究期间经历疾病复发的患者中被认为具有统计学意义,在复发患者中表达分别为 45%(MLANA)和 49%(ABCB5)(P=0·001 和 P=0·031)。对于接受非手术治疗的患者,MCAM 表达与治疗效果差相关。

结论

循环肿瘤细胞在疾病的所有阶段和手术治疗后很长时间都可检测到,即使患者被认为无疾病。具体来说,ABCB5 和 MLANA 的表达对推断疾病复发具有显著的预后价值,而 MCAM 的表达与治疗后患者的不良预后相关,证实了多标志物 qRT-PCR 作为监测疾病状态的潜在技术。

相似文献

1
Markers of circulating tumour cells in the peripheral blood of patients with melanoma correlate with disease recurrence and progression.黑色素瘤患者外周血循环肿瘤细胞标志物与疾病复发和进展相关。
Br J Dermatol. 2013 Jan;168(1):85-92. doi: 10.1111/bjd.12057. Epub 2012 Nov 15.
2
Association between circulating tumor cells and prognosis in patients with stage III melanoma with sentinel lymph node metastasis in a phase III international multicenter trial.在一项 III 期国际多中心试验中,研究了 III 期黑色素瘤伴前哨淋巴结转移患者循环肿瘤细胞与预后的关系。
J Clin Oncol. 2012 Nov 1;30(31):3819-26. doi: 10.1200/JCO.2011.40.0887. Epub 2012 Sep 24.
3
Serial monitoring of circulating melanoma cells during neoadjuvant biochemotherapy for stage III melanoma: outcome prediction in a multicenter trial.III期黑色素瘤新辅助生物化疗期间循环黑色素瘤细胞的连续监测:一项多中心试验中的结局预测
J Clin Oncol. 2005 Nov 1;23(31):8057-64. doi: 10.1200/JCO.2005.02.0958.
4
Monitoring changes in circulating tumour cells as a prognostic indicator of overall survival and treatment response in patients with metastatic melanoma.监测循环肿瘤细胞的变化,作为转移性黑色素瘤患者总生存期和治疗反应的预后指标。
BMC Cancer. 2014 Jun 11;14:423. doi: 10.1186/1471-2407-14-423.
5
Absolute quantitative PCR for detection of molecular biomarkers in melanoma patients: a preliminary report.用于检测黑色素瘤患者分子生物标志物的绝对定量PCR:初步报告。
Clin Chim Acta. 2015 Apr 15;444:242-9. doi: 10.1016/j.cca.2015.02.013. Epub 2015 Feb 26.
6
MCAM/MUC18/CD146 as a Multifaceted Warning Marker of Melanoma Progression in Liquid Biopsy.MCAM/MUC18/CD146 作为液体活检中黑色素瘤进展的多方面预警标志物。
Int J Mol Sci. 2021 Nov 17;22(22):12416. doi: 10.3390/ijms222212416.
7
Is quantitative real time polymerase chain reaction MCAM transcript assay really suitable for prognostic and predictive management of melanoma patients?定量实时聚合酶链反应检测MCAM转录本真的适用于黑色素瘤患者的预后和预测管理吗?
Br J Dermatol. 2014 Jul;171(1):190-1. doi: 10.1111/bjd.12818. Epub 2014 Jun 22.
8
Polymerase chain reaction-based detection of circulating melanoma cells as an effective marker of tumor progression. Melanoma Cooperative Group.基于聚合酶链反应检测循环黑色素瘤细胞作为肿瘤进展的有效标志物。黑色素瘤协作组。
J Clin Oncol. 1999 Jan;17(1):304-11. doi: 10.1200/JCO.1999.17.1.304.
9
Multimarker quantitative real-time PCR detection of circulating melanoma cells in peripheral blood: relation to disease stage in melanoma patients.外周血中循环黑色素瘤细胞的多标志物定量实时PCR检测:与黑色素瘤患者疾病分期的关系
Clin Chem. 2005 Jun;51(6):981-8. doi: 10.1373/clinchem.2004.045096. Epub 2005 Apr 7.
10
Serial monitoring of circulating tumor cells predicts outcome of induction biochemotherapy plus maintenance biotherapy for metastatic melanoma.循环肿瘤细胞的连续监测可预测转移性黑色素瘤诱导生物化疗加维持生物治疗的疗效。
Clin Cancer Res. 2010 Apr 15;16(8):2402-8. doi: 10.1158/1078-0432.CCR-10-0037. Epub 2010 Apr 6.

引用本文的文献

1
Pair-matched analysis of Circulating Melanoma Cells (CMCs) before and after Immunotherapy in Relation to other Melanoma-Specific Biomarkers.免疫治疗前后循环黑色素瘤细胞(CMC)与其他黑色素瘤特异性生物标志物的配对匹配分析。
J Cancer. 2025 Apr 21;16(8):2421-2433. doi: 10.7150/jca.102131. eCollection 2025.
2
New Axes of Interaction in Circ_0079593/miR-516b-5p Network in Melanoma Metastasis Cell Lines.黑色素瘤转移细胞系中Circ_0079593/miR-516b-5p网络的新相互作用轴
Genes (Basel). 2024 Dec 21;15(12):1647. doi: 10.3390/genes15121647.
3
The uniqueness of ABCB5 as a full transporter ABCB5FL and a half-transporter-like ABCB5β.

本文引用的文献

1
Melanoma survival in the United States, 1992 to 2005.美国 1992 年至 2005 年的黑色素瘤生存情况。
J Am Acad Dermatol. 2011 Nov;65(5 Suppl 1):S78-86. doi: 10.1016/j.jaad.2011.05.030.
2
Differential PAX3 functions in normal skin melanocytes and melanoma cells.PAX3 在正常皮肤黑素细胞和黑色素瘤细胞中的差异功能。
Biochem Biophys Res Commun. 2011 Aug 12;411(4):832-7. doi: 10.1016/j.bbrc.2011.07.053. Epub 2011 Jul 23.
3
Cancer statistics, 2011: the impact of eliminating socioeconomic and racial disparities on premature cancer deaths.
ABCB5作为一种完整转运体ABCB5FL和一种半转运体样ABCB5β的独特性。
Cancer Drug Resist. 2024 Aug 7;7:29. doi: 10.20517/cdr.2024.56. eCollection 2024.
4
A Review of Advanced Cutaneous Melanoma Therapies and Their Mechanisms, from Immunotherapies to Lysine Histone Methyl Transferase Inhibitors.晚期皮肤黑色素瘤治疗方法及其作用机制综述:从免疫疗法到赖氨酸组蛋白甲基转移酶抑制剂
Cancers (Basel). 2023 Dec 8;15(24):5751. doi: 10.3390/cancers15245751.
5
Circulating Melanoma Cell Numbers Correlate with TIGIT-Positive Cytotoxic T Cell Counts in Advanced-Stage Melanoma Patients.循环黑素瘤细胞数量与晚期黑素瘤患者中 TIGIT 阳性细胞毒性 T 细胞计数相关。
Cells. 2023 Mar 9;12(6):856. doi: 10.3390/cells12060856.
6
Galectin-3 Is a Natural Binding Ligand of MCAM (CD146, MUC18) in Melanoma Cells and Their Interaction Promotes Melanoma Progression.半乳糖凝集素 3 是黑素瘤细胞中 MCAM(CD146、MUC18)的天然结合配体,其相互作用促进了黑素瘤的进展。
Biomolecules. 2022 Oct 10;12(10):1451. doi: 10.3390/biom12101451.
7
Downregulation of the paired box gene 3 inhibits the progression of skin cutaneous melanoma by inhibiting c-MET tyrosine kinase : PAX3 downregulation inhibits melanoma progression.配对盒基因 3 的下调通过抑制 c-MET 酪氨酸激酶抑制皮肤黑色素瘤的进展:PAX3 的下调抑制黑色素瘤的进展。
Mol Biol Rep. 2022 Oct;49(10):9137-9145. doi: 10.1007/s11033-022-07706-5. Epub 2022 Sep 4.
8
Current Trends in Circulating Biomarkers for Melanoma Detection.黑色素瘤检测中循环生物标志物的当前趋势
Front Med (Lausanne). 2022 Apr 5;9:873728. doi: 10.3389/fmed.2022.873728. eCollection 2022.
9
Recent Developments of Circulating Tumor Cell Analysis for Monitoring Cutaneous Melanoma Patients.用于监测皮肤黑色素瘤患者的循环肿瘤细胞分析的最新进展
Cancers (Basel). 2022 Feb 9;14(4):859. doi: 10.3390/cancers14040859.
10
Liquid Biopsy in Melanoma: Significance in Diagnostics, Prediction and Treatment Monitoring.液体活检在黑色素瘤中的作用:在诊断、预测和治疗监测中的意义。
Int J Mol Sci. 2021 Sep 8;22(18):9714. doi: 10.3390/ijms22189714.
癌症统计数据,2011 年:消除社会经济和种族差异对癌症过早死亡的影响。
CA Cancer J Clin. 2011 Jul-Aug;61(4):212-36. doi: 10.3322/caac.20121. Epub 2011 Jun 17.
4
Circulating melanoma cells and survival in metastatic melanoma.循环黑素瘤细胞与转移性黑素瘤患者的生存。
Int J Oncol. 2011 Mar;38(3):755-60. doi: 10.3892/ijo.2011.896. Epub 2011 Jan 3.
5
The molecular basis of the chemosensitivity of metastatic cutaneous melanoma to chemotherapy.转移性皮肤黑色素瘤对化疗敏感性的分子基础。
J Clin Pathol. 2010 Nov;63(11):1012-20. doi: 10.1136/jcp.2010.080119. Epub 2010 Oct 5.
6
Circulating Tumor Cells and Colorectal Cancer.循环肿瘤细胞与结直肠癌
Curr Colorectal Cancer Rep. 2010 Oct 1;6(4):212-220. doi: 10.1007/s11888-010-0069-7.
7
Quantitative detection of melanoma-associated antigens by multimarker real-time RT-PCR for molecular staging: results of a 5 years study.用于分子分期的多标志物实时逆转录聚合酶链反应定量检测黑色素瘤相关抗原:一项5年研究的结果
Exp Dermatol. 2010 Nov;19(11):994-9. doi: 10.1111/j.1600-0625.2010.01123.x. Epub 2010 Aug 31.
8
PAX3 expression in normal skin melanocytes and melanocytic lesions (naevi and melanomas).PAX3 在正常皮肤黑素细胞和黑素细胞病变(痣和黑色素瘤)中的表达。
PLoS One. 2010 Apr 22;5(4):e9977. doi: 10.1371/journal.pone.0009977.
9
Serial monitoring of circulating tumor cells predicts outcome of induction biochemotherapy plus maintenance biotherapy for metastatic melanoma.循环肿瘤细胞的连续监测可预测转移性黑色素瘤诱导生物化疗加维持生物治疗的疗效。
Clin Cancer Res. 2010 Apr 15;16(8):2402-8. doi: 10.1158/1078-0432.CCR-10-0037. Epub 2010 Apr 6.
10
Tumor initiation in human malignant melanoma and potential cancer therapies.人类恶性黑色素瘤的肿瘤发生与潜在癌症疗法。
Anticancer Agents Med Chem. 2010 Feb;10(2):131-6. doi: 10.2174/187152010790909254.