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首页> 外文期刊>Tumour biology : >Vascular endothelial growth factor receptors 1,3 and caveolin-1 are implicated in colorectal cancer aggressiveness and prognosis - Correlations with epidermal growth factor receptor, CD44v6, focal adhesion kinase, and c-Met
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Vascular endothelial growth factor receptors 1,3 and caveolin-1 are implicated in colorectal cancer aggressiveness and prognosis - Correlations with epidermal growth factor receptor, CD44v6, focal adhesion kinase, and c-Met

机译:血管内皮生长因子受体1,3和caveolin-1与大肠癌的侵袭性和预后有关-与表皮生长因子受体,CD44v6,粘着斑激酶和c-Met的相关性

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Vascular endothelial growth factor receptor-1 (VEGFR-1) and caveolin-1 have been shown to act both as tumor-promoting and tumor-suppressing proteins in various malignancies as well as in colorectal cancer (CRC), while VEGFR-3's lymphagiogenic involvement and connection to tumor parameters has yielded heterogenic results. This study was designed to investigate the expression of these molecules in 183 human CRC tissue specimens and explore their effect in both clinicopathological parameters and disease prognosis. We also utilize our previous results regarding epidermal growth factor receptor (EGFR), c-Met, CD44v6, and focal adhesion kinase, in an attempt to further clarify their distinct role in tumor prognosis and their crosstalk. Caveolin-1 was more freely distributed in the neoplasms of the right colon and restricted towards the left and the rectal cancer samples (p = 0.022); VEGFR-3 was associated with higher nodal metastasis' status (p = 0.001) and staging (p = 0.006), and loss of VEGFR-1 predicted distant metastasis (p = 0.026) and advanced stage (p = 0.049). Prompted by previous reports, we performed all analyses also in the patient group of early (I and II) tumor stage where it was evident that VEGFR-1 was more frequently expressed in patients under 60 years old (p = 0.014) and VEGFR-3 was significantly elevated in left colon cancers (p = 0.039) and female patients (p = 0.038). Within the advanced stage (III and IV), the absence of VEGFR-1 exhibited a tendency for higher M status (p = 0.067) and lack of caveolin-1 signified worse AJCC classification (p = 0.053). Additionally, patient survival was influenced from VEGFR-3 (p = 0.019) for the whole sample, whereas subgroup analyses provided a correlation between caveolin-1 expression and improved survival in the early detection group of patients (p = 0.022). Using Cox regression for all available markers, EGFR, CD44v6, and VEGFR-1 emerged in this study as potential surrogate markers, the latter having positive prognostic significance. We further explored the multiple receptor correlations that were identified.
机译:血管内皮生长因子受体1(VEGFR-1)和小窝蛋白1已被证明在各种恶性肿瘤以及结直肠癌(CRC)中均作为促进肿瘤和抑制肿瘤的蛋白,而VEGFR-3的淋巴管生成与肿瘤参数的联系已产生异源性结果。这项研究旨在调查这些分子在183个人CRC组织标本中的表达,并探讨它们在临床病理参数和疾病预后中的作用。我们还利用我们先前关于表皮生长因子受体(EGFR),c-Met,CD44v6和粘着斑激酶的结果,以试图进一步阐明它们在肿瘤预后和串扰中的独特作用。 Caveolin-1更自由地分布在右结肠的肿瘤中,并局限于左和直肠癌样本(p = 0.022); VEGFR-3与更高的淋巴结转移状态(p = 0.001)和分期(p = 0.006)以及VEGFR-1的丢失预测远处转移(p = 0.026)和晚期(p = 0.049)相关。根据先前的报告,我们还在肿瘤的早期(I和II期)患者组中进行了所有分析,其中很明显,VEGFR-1在60岁以下患者中更频繁表达(p = 0.014)和VEGFR-3在左结肠癌(p = 0.039)和女性患者(p = 0.038)中,mRNA明显升高。在晚期阶段(III和IV),缺乏VEGFR-1表现出较高的M状态(p = 0.067),而缺乏caveolin-1则表明AJCC分类较差(p = 0.053)。此外,整个样品的患者生存率均受VEGFR-3的影响(p = 0.019),而亚组分析提供了Caveolin-1表达与早期检测患者生存率提高之间的相关性(p = 0.022)。使用Cox回归分析所有可用标记,EGFR,CD44v6和VEGFR-1在本研究中作为潜在的替代标记出现,后者具有积极的预后意义。我们进一步探讨了已鉴定的多种受体相关性。

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