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肿瘤内皮标志物 7(TEM-7):一种新的抗血管生成治疗靶点。

Tumor endothelial marker 7 (TEM-7): a novel target for antiangiogenic therapy.

机构信息

Genzyme Corporation, 49 New York Ave., Framingham, MA 01701, USA.

出版信息

Microvasc Res. 2011 Nov;82(3):253-62. doi: 10.1016/j.mvr.2011.09.004. Epub 2011 Sep 17.

Abstract

Antiangiogenesis has been validated as a therapeutic strategy to treat cancer, however, a need remains to identify new targets and therapies for specific diseases and to improve clinical benefit from antiangiogenic agents. Tumor endothelial marker 7 (TEM-7) was investigated as a possible target for therapeutic antiangiogenic intervention in cancer. TEM-7 expression was assessed by in situ hybridization or by immunohistochemistry (IHC) in 130 formalin-fixed paraffin-embedded (FFPE) and 410 frozen human clinical specimens of cancer plus 301 normal tissue samples. In vitro TEM-7 expression was evaluated in 4 human endothelial cell models and in 32 human cancer cell lines by RT-PCR and flow cytometry. An anti-TEM-7 antibody was tested in vitro on human SKOV3 ovarian and MDA-MB-231 breast carcinoma cells that expressed TEM-7 in antibody-dependent cellular cytotoxicity (ADCC) and phagocytosis assays. In frozen tumor tissues, TEM-7 mRNA and protein was detected in all but one of the cancer types tested and was infrequently expressed in normal frozen tissues. In FFPE tumor tissues, TEM-7 protein was detected by IHC in colon, breast, lung, bladder, ovarian and endometrial cancers and in sarcomas. TEM-7 protein was not detected in head and neck, prostate or liver cancers. TEM-7 expression was restricted to the vasculature and was absent from tumor cells. In vitro, TEM-7 was not detected in human microvascular endothelial cells (HMVEC) or human umbilical vein endothelial cells (HUVEC) but was induced in endothelial precursor/progenitor cells (EPC) in the presence of the mitogen phorbol ester PMA. An anti-TEM-7 antibody mediated ADCC and phagocytosis in SKOV3 and MDA-MB-231 cell lines infected with an adenovirus expressing TEM-7. These data demonstrate that TEM-7 is a vascular protein associated with angiogenic states. TEM-7 is a novel and attractive target for antiangiogenic therapy.

摘要

抗血管生成已被验证为治疗癌症的一种治疗策略,然而,仍然需要确定针对特定疾病的新靶点和疗法,并提高抗血管生成药物的临床获益。肿瘤内皮标志物 7(TEM-7)被研究为癌症治疗性抗血管生成干预的可能靶点。通过原位杂交或免疫组织化学(IHC)在 130 个福尔马林固定石蜡包埋(FFPE)和 410 个冷冻的人类临床癌症标本以及 301 个正常组织样本中评估 TEM-7 的表达。通过 RT-PCR 和流式细胞术在 4 个人内皮细胞模型和 32 个人癌细胞系中评估体外 TEM-7 表达。在依赖抗体的细胞毒性(ADCC)和吞噬作用测定中,在体外测试了抗 TEM-7 抗体对表达 TEM-7 的 SKOV3 卵巢和 MDA-MB-231 乳腺癌细胞的作用。在冷冻肿瘤组织中,除一种测试的癌症类型外,所有癌症类型均检测到 TEM-7 mRNA 和蛋白,并且在正常冷冻组织中很少表达。在 FFPE 肿瘤组织中,通过 IHC 在结肠、乳腺、肺、膀胱、卵巢和子宫内膜癌以及肉瘤中检测到 TEM-7 蛋白。在头颈部、前列腺或肝癌中未检测到 TEM-7 蛋白。TEM-7 表达仅限于脉管系统,不存在于肿瘤细胞中。在体外,在人微血管内皮细胞(HMVEC)或人脐静脉内皮细胞(HUVEC)中未检测到 TEM-7,但在存在有丝分裂原佛波醇酯 PMA 的情况下,在内皮前体/祖细胞(EPC)中诱导。携带表达 TEM-7 的腺病毒感染的 SKOV3 和 MDA-MB-231 细胞系中,抗 TEM-7 抗体介导 ADCC 和吞噬作用。这些数据表明,TEM-7 是一种与血管生成状态相关的血管蛋白。TEM-7 是一种新的有吸引力的抗血管生成治疗靶点。

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