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Tie2/Tek在乳腺肿瘤脉管系统中的表达为评估肿瘤血管生成提供了一种新的标志物。

Expression of Tie2/Tek in breast tumour vasculature provides a new marker for evaluation of tumour angiogenesis.

作者信息

Peters K G, Coogan A, Berry D, Marks J, Iglehart J D, Kontos C D, Rao P, Sankar S, Trogan E

机构信息

Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Br J Cancer. 1998;77(1):51-6. doi: 10.1038/bjc.1998.8.

DOI:10.1038/bjc.1998.8
PMID:9459145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2151265/
Abstract

Endothelial receptor tyrosine kinases may play important roles in pathological vascular growth, particularly in tumours. In this study, immunohistochemistry was used to evaluate the expression of a novel endothelial receptor tyrosine kinase, Tie2/Tek, in the endothelium of vascular 'hotspots' in normal breast tissue (n = 10), benign breast lesions (n = 10) and in breast tumours (n = 123). Tie2 expression was detected in the endothelium of all breast tissues examined. However, the strongest expression of Tie-2 was seen in vascular 'hot spots' within the inflammatory infiltrate at the periphery of invasive tumours. Moreover, the proportion of Tie2-positive vessels (Tie2 counts/CD31 counts) was significantly higher in breast tumours than the proportion of Tie2-positive vessels in either normal breast tissue or benign breast lesions (P = 0.004 and 0.0001 respectively). These data are consistent with a role for Tie2 in tumour angiogenesis and demonstrate the potential use of Tie2 expression as a novel marker of the tumour vasculature.

摘要

内皮受体酪氨酸激酶可能在病理性血管生长中发挥重要作用,尤其是在肿瘤中。在本研究中,采用免疫组织化学方法评估一种新型内皮受体酪氨酸激酶Tie2/Tek在正常乳腺组织(n = 10)、乳腺良性病变(n = 10)和乳腺肿瘤(n = 123)血管“热点”内皮中的表达。在所检查的所有乳腺组织的内皮中均检测到Tie2表达。然而,在浸润性肿瘤周边炎症浸润内的血管“热点”中观察到Tie-2的最强表达。此外,乳腺肿瘤中Tie2阳性血管的比例(Tie2计数/CD31计数)显著高于正常乳腺组织或乳腺良性病变中Tie2阳性血管的比例(分别为P = 0.004和0.0001)。这些数据与Tie2在肿瘤血管生成中的作用一致,并证明Tie2表达作为肿瘤脉管系统新标志物的潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b01/2151265/20b6218f08fb/brjcancer00077-0056-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b01/2151265/a908418e1960/brjcancer00077-0056-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b01/2151265/20b6218f08fb/brjcancer00077-0056-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b01/2151265/a908418e1960/brjcancer00077-0056-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b01/2151265/20b6218f08fb/brjcancer00077-0056-b.jpg

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本文引用的文献

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Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2.受体酪氨酸激酶TIE2激活突变引起的血管发育异常。
Cell. 1996 Dec 27;87(7):1181-90. doi: 10.1016/s0092-8674(00)81814-0.
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Blood vessel formation: what is its molecular basis?血管形成:其分子基础是什么?
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Lactate engages receptor tyrosine kinases Axl, Tie2, and vascular endothelial growth factor receptor 2 to activate phosphoinositide 3-kinase/Akt and promote angiogenesis.乳酸通过结合受体酪氨酸激酶 Axl、Tie2 和血管内皮生长因子受体 2 来激活磷酸肌醇 3-激酶/蛋白激酶 B(Akt)并促进血管生成。
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Tumor angiogenesis and lymphangiogenesis: tumor/endothelial crosstalk and cellular/microenvironmental signaling mechanisms.肿瘤血管生成和淋巴管生成:肿瘤/内皮细胞串扰和细胞/微环境信号机制。
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Endothelial Tie growth factor receptor provides antigenic marker for assessment of breast cancer angiogenesis.内皮 Tie 生长因子受体为评估乳腺癌血管生成提供抗原标志物。
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Tie-1 and tie-2 define another class of putative receptor tyrosine kinase genes expressed in early embryonic vascular system.Tie-1和Tie-2定义了另一类在早期胚胎血管系统中表达的假定受体酪氨酸激酶基因。
Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9355-8. doi: 10.1073/pnas.90.20.9355.