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微小 RNA-126 和表皮生长因子样结构域 7——转移性结直肠癌中重要的血管生成对。来自北欧 ACT 试验的结果。

MicroRNA-126 and epidermal growth factor-like domain 7-an angiogenic couple of importance in metastatic colorectal cancer. Results from the Nordic ACT trial.

机构信息

Department of Oncology, Vejle Hospital, Lillebaelt Hospital, Denmark.

出版信息

Br J Cancer. 2013 Sep 3;109(5):1243-51. doi: 10.1038/bjc.2013.448. Epub 2013 Aug 6.

Abstract

BACKGROUND

This study investigated the clinical importance of linked angiogenetic biomarkers to chemotherapy, combined with the anti-vascular endothelial growth factor A (anti-VEGF-A), as a first-line treatment in patients with metastatic colorectal cancer (mCRC).

METHODS

A total of 230 patients from a randomised phase III study were included. The primary microRNA-126 (pri-miRNA-126) A24G single-nucleotide polymorphism and the mature miRNA-126 were analysed by PCR using genomic DNA (full blood) and formalin-fixed paraffin-embedded tissue sections, respectively. The epidermal growth factor-like domain 7 (EGFL7) protein was visualised and quantified using immunohistochemistry.

RESULTS

High tumour expression of miRNA-126 was significantly related to a longer progression-free survival. The independent prognostic value of miRNA-126 was confirmed using a Cox regression analysis (hazard ratio=0.49, 95% confidence interval=0.29-0.84, P=0.009). Although not significant, a relationship between EGFL7 expression and response rates is suggested, with EGFL7 expression at the invasive front being lower in responding patients than in the non-responders (P=0.063).

CONCLUSION

The results validate the previous findings on the prognostic value of miRNA-126 in mCRC and may suggest a relationship between treatment efficacy and EGFL7 expression. As miRNA-126 may target VEGF-A as well as EGFL7, the results may provide predictive information in relation to next-generation anti-angiogenetics.

摘要

背景

本研究探讨了与化疗相关的连接血管生成生物标志物的临床重要性,联合抗血管内皮生长因子 A(抗-VEGF-A)作为转移性结直肠癌(mCRC)患者的一线治疗。

方法

共纳入来自一项随机 III 期研究的 230 例患者。使用聚合酶链反应(PCR)分别分析了微小 RNA-126(miRNA-126)的 A24G 单核苷酸多态性和成熟 miRNA-126,使用基因组 DNA(全血)和福尔马林固定石蜡包埋组织切片。使用免疫组织化学可视化和定量表皮生长因子样结构域 7(EGFL7)蛋白。

结果

肿瘤中高表达 miRNA-126 与无进展生存期延长显著相关。使用 Cox 回归分析证实了 miRNA-126 的独立预后价值(危险比=0.49,95%置信区间=0.29-0.84,P=0.009)。尽管没有统计学意义,但 EGFL7 表达与缓解率之间存在一定关系,缓解患者的侵袭前沿 EGFL7 表达低于非缓解患者(P=0.063)。

结论

这些结果验证了 miRNA-126 在 mCRC 中的预后价值的先前发现,并且可能提示治疗效果与 EGFL7 表达之间存在关系。由于 miRNA-126 可能靶向 VEGF-A 和 EGFL7,因此这些结果可能为下一代抗血管生成药物提供预测信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/599b/3778299/4fed1e98b56f/bjc2013448f1.jpg

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