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本文引用的文献

1
Correlation of MRI biomarkers with tumor necrosis in Hras5 tumor xenograft in athymic rats.无胸腺大鼠Hras5肿瘤异种移植中MRI生物标志物与肿瘤坏死的相关性
Neoplasia. 2007 May;9(5):382-91. doi: 10.1593/neo.07145.
2
Imaging of VEGF receptor kinase inhibitor-induced antiangiogenic effects in drug-resistant human adenocarcinoma model.VEGF受体激酶抑制剂在耐药性人腺癌模型中诱导的抗血管生成作用的成像
Neoplasia. 2005 Sep;7(9):847-53. doi: 10.1593/neo.05139.
3
Vessel size imaging in humans.人体血管大小成像。
Magn Reson Med. 2005 Mar;53(3):553-63. doi: 10.1002/mrm.20383.
4
Serial tumour blood-flow measurements in androgen-dependent and -independent Shionogi tumour models.在雄激素依赖型和非依赖型狮王瘤模型中进行肿瘤血流的连续测量。
BJU Int. 2005 Mar;95(4):644-9. doi: 10.1111/j.1464-410X.2005.05355.x.
5
Vessel size imaging using low intravascular contrast agent concentrations.使用低血管内造影剂浓度的血管大小成像。
MAGMA. 2004 Dec;17(3-6):313-6. doi: 10.1007/s10334-004-0067-3. Epub 2004 Dec 1.
6
In vivo assessment of tumoral angiogenesis.肿瘤血管生成的体内评估。
Magn Reson Med. 2004 Mar;51(3):533-41. doi: 10.1002/mrm.20017.
7
Cancer statistics, 2004.2004年癌症统计数据。
CA Cancer J Clin. 2004 Jan-Feb;54(1):8-29. doi: 10.3322/canjclin.54.1.8.
8
Effects of overexpression of dimethylarginine dimethylaminohydrolase on tumor angiogenesis assessed by susceptibility magnetic resonance imaging.通过敏感性磁共振成像评估二甲基精氨酸二甲胺水解酶过表达对肿瘤血管生成的影响。
Cancer Res. 2003 Aug 15;63(16):4960-6.
9
Tumor vascular architecture and function evaluated by non-invasive susceptibility MRI methods and immunohistochemistry.通过非侵入性磁共振成像敏感性方法和免疫组织化学评估肿瘤血管结构和功能。
J Magn Reson Imaging. 2003 Apr;17(4):445-54. doi: 10.1002/jmri.10274.
10
Angiogenesis modulation in cancer research: novel clinical approaches.癌症研究中的血管生成调控:新型临床方法。
Nat Rev Drug Discov. 2002 Jun;1(6):415-26. doi: 10.1038/nrd819.

激素依赖性史氏肿瘤血管生成的纵向研究。

Longitudinal studies of angiogenesis in hormone-dependent Shionogi tumors.

作者信息

Wade Trevor P, Kozlowski Piotr

机构信息

Department of Physics and Astronomy, University of British Columbia, Vancouver, BC, Canada.

出版信息

Neoplasia. 2007 Jul;9(7):563-8. doi: 10.1593/neo.07313.

DOI:10.1593/neo.07313
PMID:17710159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1939931/
Abstract

Vessel size imaging was used to assess changes in the average vessel size of Shionogi tumors throughout the tumor growth cycle. Changes in R(2) and R(2)* relaxivities caused by the injection of a superparamagnetic contrast agent (ferumoxtran-10) were measured using a 2.35-T animal magnetic resonance imaging system, and average vessel size index (VSI) was calculated for each stage of tumor progression: growth, regression, and relapse. Statistical analysis using Spearman rank correlation test showed no dependence between vessel size and tumor volume at any stage of the tumor growth cycle. Paired Student's t test was used to assess the statistical significance of the differences in average vessel size for the three stages of the tumor growth cycle. The average VSI for regressing tumors (15.1 +/- 6.6 microm) was significantly lower than that for growing tumors (35.2 +/- 25.5 microm; P < .01). Relapsing tumors also had an average VSI (45.4 +/- 41.8 microm) higher than that of regressing tumors, although the difference was not statistically significant (P = .067). This study shows that VSI imaging is a viable method for the noninvasive monitoring of angiogenesis during the progression of a Shionogi tumor from androgen dependence to androgen independence.

摘要

血管大小成像用于评估在整个肿瘤生长周期中,Shionogi肿瘤的平均血管大小变化。使用2.35-T动物磁共振成像系统测量注射超顺磁性造影剂(ferumoxtran-10)后引起的R(2)和R(2)*弛豫率变化,并针对肿瘤进展的每个阶段(生长、消退和复发)计算平均血管大小指数(VSI)。使用Spearman等级相关检验进行的统计分析表明,在肿瘤生长周期的任何阶段,血管大小与肿瘤体积之间均无相关性。采用配对学生t检验评估肿瘤生长周期三个阶段的平均血管大小差异的统计学意义。消退期肿瘤的平均VSI(15.1±6.6微米)显著低于生长期肿瘤(35.2±25.5微米;P <.01)。复发期肿瘤的平均VSI(45.4±41.8微米)也高于消退期肿瘤,尽管差异无统计学意义(P = 0.067)。本研究表明,VSI成像对于在Shionogi肿瘤从雄激素依赖向雄激素非依赖进展过程中无创监测血管生成是一种可行的方法。