首页> 外文期刊>Digestive Diseases and Sciences >The simultaneous expression of peroxisome proliferator-activated receptor delta and cyclooxygenase-2 may enhance angiogenesis and tumor venous invasion in tissues of colorectal cancers.
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The simultaneous expression of peroxisome proliferator-activated receptor delta and cyclooxygenase-2 may enhance angiogenesis and tumor venous invasion in tissues of colorectal cancers.

机译:过氧化物酶体增殖物激活的受体δ和环氧合酶-2的同时表达可能增强大肠癌组织中的血管生成和肿瘤静脉侵袭。

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摘要

We conducted this study to evaluate the impact of the expression of peroxisome proliferator-activated receptor delta on angiogenesis in tissue samples of colorectal cancer. We examined 52 samples of primary human colorectal carcinomas and matched normal adjacent tissues to evaluate the expression of peroxisome proliferator-activated receptor delta, cyclooxygenase-2, vascular endothelial growth factor-A, and CD34 through immunohistochemical analysis. Peroxisome proliferator-activated receptor delta was expressed in 25 (48.1%), and cyclooxygenase-2 was expressed in 26 (50.0%) of total colorectal cancer tissues. Tissue samples were divided into four groups, according to the expression of peroxisome proliferator-activated receptor delta and cyclooxygenase-2. The positive rate of vascular endothelial growth factor-A, the levels of microvascular density, and the incidence of venous vessel invasion in peroxisome proliferator-activated receptor delta (+)/cyclooxygenase-2 (+) samples exceeded significantly those in the other three groups of tissue samples (P<0.05). The results suggest that the axis of the cyclooxygenase-2/peroxisome proliferator-activated receptor delta signal pathway might play a crucial role in the development of colorectal cancers by enhancing angiogenesis.
机译:我们进行了这项研究,以评估过氧化物酶体增殖物激活受体δ的表达对结直肠癌组织样本中血管生成的影响。我们检查了52例原发性人类大肠癌和匹配的正常邻近组织,以通过免疫组织化学分析评估过氧化物酶体增殖物激活受体δ,环氧合酶-2,血管内皮生长因子-A和CD34的表达。过氧化物酶体增殖物激活的受体δ在总的大肠癌组织中表达为25(48.1%),而环氧合酶-2在26(表达为50.0%)中表达。根据过氧化物酶体增殖物激活受体δ和环氧合酶-2的表达,将组织样品分为四组。过氧化物酶体增殖物激活受体δ(+)/环氧合酶-2(+)样品中血管内皮生长因子-A的阳性率,微血管密度水平和静脉血管侵袭的发生率明显超过其他三组组织样本数(P <0.05)。结果表明,环氧合酶-2 /过氧化物酶体增殖物激活的受体δ信号通路的轴可能通过增强血管生成在结直肠癌的发展中起关键作用。

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