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异体输血后血管生成增强。

Enhanced angiogenesis following allogeneic blood transfusion.

作者信息

Patel H B, Nasir F A, Nash G F, Scully M F, Kakkar A K

机构信息

Thrombosis Research Institute, Emmanual Kaye Building, Manresa Road, London, UK.

出版信息

Clin Lab Haematol. 2004 Apr;26(2):129-35. doi: 10.1111/j.1365-2257.2004.00589.x.

Abstract

Blood transfusions are associated with recurrence of solid cancers. Angiogenesis is essential for cancer growth. Our aim was to determine for the first time in a prospective cohort study the effect of prestorage allogeneic leucodepleted SAGM (saline, adenine, glucose, mannitol) red cell transfusion on angiogenic factor levels and in vitro angiogenesis. Forty pretransfusion adult hospital inpatients were selected consecutively. Serum vascular endothelial growth factor (VEGF) and endostatin were measured in each patient before and after prestorage allogeneic leucodepleted SAGM red cell transfusion. All samples were exposed to an in vitro endothelial cell proliferation assay and 10 sample groups were also exposed to an in vitro whole angiogenesis assay. The median number of units transfused was 2 (minimum-maximum, 2-4). Twenty-nine (73%) patients had a rise in VEGF, with an overall increase of 118 pg/ml (quartiles -5, 306; P < 0.01). Twenty-eight (70%) patients had a decrease in endostatin, with an overall reduction of 1.2 ng/ml (quartiles 4.0, 0.0; P = 0.017). There was an overall 33% increase in endothelial cell proliferation (P < 0.01) and a 9.4% increase in in vitro whole assay angiogenesis (P < 0.01). Prestorage allogeneic leucodepleted SAGM red cell transfusions are associated with a favourable angiogenic factor imbalance and an elevation in in vitro angiogenesis.

摘要

输血与实体癌复发有关。血管生成对癌症生长至关重要。我们的目的是在一项前瞻性队列研究中首次确定储存前异体白细胞滤除的SAGM(生理盐水、腺嘌呤、葡萄糖、甘露醇)红细胞输注对血管生成因子水平和体外血管生成的影响。连续挑选了40名输血前的成年住院患者。在储存前异体白细胞滤除的SAGM红细胞输注前后,对每位患者的血清血管内皮生长因子(VEGF)和内皮抑素进行了测量。所有样本都进行了体外内皮细胞增殖试验,10个样本组还进行了体外全血管生成试验。输注的单位中位数为2(最小值 - 最大值,2 - 4)。29名(73%)患者的VEGF升高,总体增加了118 pg/ml(四分位数 -5,306;P < 0.01)。28名(70%)患者的内皮抑素降低,总体减少了1.2 ng/ml(四分位数4.0,0.0;P = 0.017)。内皮细胞增殖总体增加了33%(P < 0.01),体外全试验血管生成增加了9.4%(P < 0.01)。储存前异体白细胞滤除的SAGM红细胞输注与有利的血管生成因子失衡和体外血管生成增加有关。

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