Mouawad Roger, Spano Jean-Philippe, Comperat Eva, Capron Frederique, Khayat David
AP-HP, Salpêtrière Hospital, University of Pierre & Marie Curie Paris 6, Laboratory of the Medical Oncology Department, 47 Boulevard de l'Hôpital, 75013 Paris, France.
Eur J Cancer. 2009 May;45(8):1407-14. doi: 10.1016/j.ejca.2008.12.015. Epub 2009 Jan 20.
The presence of metastases in regional lymph nodes is a strong indicator of poor patient survival in many types of cancer. It has recently been shown that vascular endothelial growth factor-C (VEGF-C), and its receptor VEGFR-3, may play a pivotal role in the promotion of metastasis to regional lymph nodes. This study was designed to detect and evaluate whether the expression of VEGFR-3 or its soluble form plays a role in metastatic malignant melanoma and to determine the relationship with clinicopathological parameters and patients outcome.
VEGFR-3 expression on melanoma tumour was evaluated by immunohistochemical study. Using a sensitive enzyme-linked immunosorbent assay, sVEGFR-3 was measured in sera of 60 metastatic melanoma patients in comparison with 30 healthy controls.
Immunohistochemical study demonstrated a high expression of VEGFR-3 in melanoma cells. Median level of pre-treatment sVEGFR-3 was significantly higher (p=0.00001) in melanoma patients as compared to healthy donors. No association was noted between VEGFR-3 in situ or in sera and gender, age or LDH level. Median serum VEGFR-3 levels were significantly higher in patients with high tumour burden as compared to those with low tumour burden (p=0.013) as well as in non-responding patients (n=33) as compared to responding ones (n=27). Finally, low level of VEGFR-3 was also related positively to disease free survival (X(2)=3.85, p=0.022).
These results suggest that the expression and high pre-treatment sVEGFR-3 level are significantly correlated to poorer prognosis, and may be promising targets for new therapeutic strategies in melanoma disease.
区域淋巴结转移的存在是多种癌症患者生存预后不良的有力指标。最近的研究表明,血管内皮生长因子-C(VEGF-C)及其受体VEGFR-3可能在促进区域淋巴结转移中起关键作用。本研究旨在检测和评估VEGFR-3及其可溶性形式的表达在转移性恶性黑色素瘤中是否起作用,并确定其与临床病理参数及患者预后的关系。
通过免疫组织化学研究评估黑色素瘤肿瘤上VEGFR-3的表达。使用灵敏的酶联免疫吸附测定法,检测60例转移性黑色素瘤患者血清中的可溶性VEGFR-3(sVEGFR-3),并与30名健康对照者进行比较。
免疫组织化学研究显示黑色素瘤细胞中VEGFR-3高表达。与健康供者相比,黑色素瘤患者治疗前sVEGFR-3的中位水平显著更高(p = 0.00001)。未发现原位或血清中的VEGFR-3与性别、年龄或乳酸脱氢酶水平之间存在关联。肿瘤负荷高的患者血清VEGFR-3中位水平显著高于肿瘤负荷低的患者(p = 0.013),无反应患者(n = 33)的血清VEGFR-3中位水平也显著高于有反应患者(n = 27)。最后,VEGFR-3低水平也与无病生存期呈正相关(X(2)=3.85,p = 0.022)。
这些结果表明,VEGFR-3的表达及治疗前sVEGFR-3高水平与较差的预后显著相关,可能是黑色素瘤疾病新治疗策略的有前景的靶点。