内皮素在转移性黑色素瘤肿瘤微环境血管系统中的表达:潜在的治疗意义。

Q2 Medicine Cancer Microenvironment Pub Date : 2015-08-01 Epub Date: 2015-06-18 DOI:10.1007/s12307-015-0168-8
Eiji Kiyohara, Nicholas Donovan, Ling Takeshima, Sharon Huang, James S Wilmott, Richard A Scolyer, Peter Jones, Elizabeth B Somers, Daniel J O'Shannessy, Dave S B Hoon
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引用次数: 20

摘要

Ontuxizumab (MORAb-004)是一种靶向内毒素(TEM-1, CD248)的人源化重组抗体。我们使用抗内啡肽大鼠抗MAb 9G5对转移性黑色素瘤标本中的内啡肽表达进行了分析,以确定内啡肽在肿瘤微环境血管系统中作为治疗靶点的潜力。在美国癌症联合委员会(AJCC) III期(n = 18)和IV期(n = 48)标本的血管中,采用免疫组化(IHC)检测石蜡包埋档案组织块(PEAT)黑色素瘤组织中内毒素的表达。进一步在包括136例IV期和33例配对III期黑色素瘤标本的TMA上进行内皮素表达的免疫组化。BRAF突变(mt)也在个体黑色素瘤标本和TMA中进行了评估。分析显示70%的黑色素瘤标本(n = 46)内啡肽表达阳性。内皮素和BRAFmt在III期和IV期标本中的表达无显著差异。86% (n = 117)的IV期TMA标本中检测到内啡肽表达,而29例正常组织对照中未检测到内啡肽表达。MAb 9G5检测大多数转移性黑色素瘤组织微环境肿瘤血管中内皮素的存在,而不考虑临床分期和是否存在BRAFmt。相对于正常组织,内啡肽在转移性黑色素瘤中的选择性表达可能是一个潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Endosialin Expression in Metastatic Melanoma Tumor Microenvironment Vasculature: Potential Therapeutic Implications.

Ontuxizumab (MORAb-004) is a humanized recombinant antibody targeting endosialin (TEM-1, CD248). We conducted an analysis of endosialin expression in metastatic melanoma specimens using the anti-endosialin rat anti- MAb 9G5, in order to determine the potential of endosialin as a therapeutic target within the tumor microenvironment vasculature. Endosialin expression in paraffin-embedded archival tissue block (PEAT) melanoma tissues was assessed using immunohistochemistry (IHC) with the anti-endosialin, MAb 9G5, in the vessels of American Joint Commission on Cancer (AJCC) Stage III (n = 18) and Stage IV (n = 48) specimens. IHC for endosialin expression was further performed on a TMA that included 136 Stage IV and 33 paired Stage III melanoma specimens. BRAF mutation (mt) was also evaluated in individual melanoma specimens and as well as the TMA. Analysis showed 70 % of melanoma specimens (n = 46) were positive for endosialin expression. There was no significant difference in endosialin and BRAFmt expression between stages III vs. IV specimens. Endosialin expression was detected in 86 % (n = 117) of stage IV TMA specimens, while no expression was detected in 29 normal tissue controls. MAb 9G5 detects the presence of endosialin in the microenvironment tumor vasculature of most metastatic melanoma tissues, regardless of clinical stage and presence of BRAFmt. Endosialin may be a potential therapeutic target by virtue of its selective expression in metastatic melanoma relative to normal tissues.

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来源期刊
Cancer Microenvironment
Cancer Microenvironment Medicine-Oncology
CiteScore
4.90
自引率
0.00%
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0
期刊介绍: Cancer Microenvironment is the official journal of the International Cancer Microenvironment Society (ICMS). It publishes original studies in all aspects of basic, clinical and translational research devoted to the study of cancer microenvironment. It also features reports on clinical trials. Coverage in Cancer Microenvironment includes: regulation of gene expression in the cancer microenvironment; innate and adaptive immunity in the cancer microenvironment, inflammation and cancer; tumor-associated stroma and extracellular matrix, tumor-endothelium interactions (angiogenesis, extravasation), cancer stem cells, the metastatic niche, targeting the tumor microenvironment: preclinical and clinical trials.
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