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恶性黑素瘤患者循环 microRNA-221 水平作为一种新的肿瘤标志物。

The circulating microRNA-221 level in patients with malignant melanoma as a new tumor marker.

机构信息

Department of Dermatology and Plastic Surgery, Faculty of Life Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto, Japan.

出版信息

J Dermatol Sci. 2011 Mar;61(3):187-93. doi: 10.1016/j.jdermsci.2010.12.010. Epub 2011 Jan 13.

DOI:10.1016/j.jdermsci.2010.12.010
PMID:21273047
Abstract

BACKGROUND

MicroRNA-221 (miR-221) is known to be abnormally expressed in malignant melanoma (MM) cells, and it favors the induction of the malignant phenotype through down-modulation of p27Kip1/CDKN1B and the c-KIT receptor. This suggests that the serum level of miR-221 might increase in patients with MM and thus could be used as a new tumor marker.

OBJECTIVE

To evaluate the possibility that the serum miR-221 level can be a marker of MM.

METHODS

Serum samples were obtained from 94 MM patients and 20 healthy controls. MicroRNAs were purified from serum, and miR-221 levels were measured by quantitative real-time polymerase chain reaction.

RESULTS

Circulating miR-221 was detectable and could be quantified in serum samples. MM patients had significantly higher miR-221 levels than healthy controls. Among the MM patients, the miR-221 levels were significantly increased in patients with stage I-IV MM compared to those with MM in situ, and the levels were correlated with tumor thickness. Moreover, a longitudinal study revealed a tendency for the miR-221 levels to decrease after surgical removal of the primary tumor, and to increase again at recurrence.

CONCLUSIONS

Serum levels of miR-221 were significantly increased in MM patients and may be useful not only for the diagnosis of MM, but also for the differentiating MM in situ from stage I-IV MM, and for evaluating tumor progression and monitoring patients during the follow-up period. In addition, considering that the serum levels of miR-221 were correlated with tumor thickness, miR-221 might also be useful as a prognostic marker for patients with MM.

摘要

背景

已知 microRNA-221(miR-221)在恶性黑色素瘤(MM)细胞中异常表达,通过下调 p27Kip1/CDKN1B 和 c-KIT 受体,促进恶性表型的诱导。这表明 MM 患者的血清 miR-221 水平可能升高,因此可以作为一种新的肿瘤标志物。

目的

评估血清 miR-221 水平是否可以作为 MM 的标志物。

方法

从 94 例 MM 患者和 20 例健康对照者中获得血清样本。从血清中纯化 microRNAs,通过实时定量聚合酶链反应测量 miR-221 水平。

结果

循环 miR-221 可在血清样本中检测到并可定量。MM 患者的 miR-221 水平明显高于健康对照组。在 MM 患者中,I-IV 期 MM 患者的 miR-221 水平明显高于原位 MM 患者,且与肿瘤厚度相关。此外,纵向研究显示,原发性肿瘤切除后 miR-221 水平有下降趋势,复发时再次升高。

结论

MM 患者血清 miR-221 水平明显升高,不仅对 MM 的诊断有用,而且对原位 MM 与 I-IV 期 MM 的鉴别、肿瘤进展的评估以及随访期间患者的监测也有用。此外,考虑到血清 miR-221 水平与肿瘤厚度相关,miR-221 也可能作为 MM 患者的预后标志物。

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The circulating microRNA-221 level in patients with malignant melanoma as a new tumor marker.恶性黑素瘤患者循环 microRNA-221 水平作为一种新的肿瘤标志物。
J Dermatol Sci. 2011 Mar;61(3):187-93. doi: 10.1016/j.jdermsci.2010.12.010. Epub 2011 Jan 13.
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