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首页> 外文期刊>Oncology letters >Microvascular density and endothelial area correlate with Ki-67 proliferative index in surgically-treated pancreatic ductal adenocarcinoma patients
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Microvascular density and endothelial area correlate with Ki-67 proliferative index in surgically-treated pancreatic ductal adenocarcinoma patients

机译:手术治疗的胰腺导管腺癌患者的微血管密度和内皮面积与Ki-67增殖指数相关

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Previous experimental and clinical data have indicated that tumour cell proliferation is associated with angiogenesis; in addition, an increased microvascular density (MVD) of tumours has been associated with poor prognosis in solid and haematological malignancies. However, limited data exists regarding the association between tumour cell proliferation and angiogenesis in primary tumour tissue from pancreatic ductal adenocarcinoma (PDAC) patients; therefore, the present study aimed to investigate this association. A series of 31 PDAC patients with stage Tumour (T)(2-3) Node (N)(0-1) Metastasis (M)(0) were recruited into the present study and subsequently underwent surgery. PDAC tissue and adjacent normal tissue (ANT), resected during surgery, were evaluated using immunohistochemistry and image analysis methods to determine MVD, endothelial area (EA) and Ki-67 expression, which is an indicator of cell proliferation rate. The results demonstrated a correlation between the above parameters with each other as well as the main clinico-pathological features of PDAC. Significant differences were identified in MVD, EA and Ki-67 proliferation index between PDAC and ANT. It was demonstrated that MVD, EA and Ki-67 proliferation index were significantly correlated with each other in tumour tissue (r=0.69-0.81; P=0.001-0.003). However, no other significant correlations were identified. These data therefore suggested that angiogenesis and cell proliferation rate were significantly increased in PDAC compared with ANT, which provides a biological basis for the potential use of novel combinations of angiogenesis inhibitors and anti-proliferative chemotherapeutic drugs in the treatment of PDAC.
机译:先前的实验和临床数据表明,肿瘤细胞的增殖与血管生成有关。另外,增加的肿瘤微血管密度(MVD)与实体和血液恶性肿瘤的不良预后有关。然而,关于胰腺导管腺癌(PDAC)患者原发肿瘤组织中肿瘤细胞增殖与血管生成之间关系的数据有限。因此,本研究旨在调查这种关联。本研究招募了31例PDAC患者,这些患者具有肿瘤(T)(2-3)淋巴结(N)(0-1)转移(M)(0)的阶段,随后进行了手术。使用免疫组织化学和图像分析方法评估手术期间切除的PDAC组织和邻近正常组织(ANT),以确定MVD,内皮面积(EA)和Ki-67表达,这是细胞增殖速率的指标。结果表明上述参数彼此之间以及PDAC的主要临床病理特征之间的相关性。在PDAC和ANT之间的MVD,EA和Ki-67增殖指数中发现了显着差异。证实在肿瘤组织中MVD,EA和Ki-67增殖指数彼此显着相关(r = 0.69-0.81; P = 0.001-0.003)。但是,没有其他显着的相关性被确定。因此,这些数据表明,与ANT相比,PDAC中的血管生成和细胞增殖速率显着增加,这为血管生成抑制剂和抗增殖化学治疗药物的新型组合潜在地用于治疗PDAC提供了生物学基础。

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