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S100P、晚期糖基化终产物受体和 ezrin 在恶性黑色素瘤中的上调。

Upregulation of S100P, receptor for advanced glycation end products and ezrin in malignant melanoma.

机构信息

Division of Skin Surface Sensing, Kyushu University, Fukuoka, Japan; Department of Dermatology, Kyushu University, Fukuoka, Japan.

出版信息

J Dermatol. 2013 Dec;40(12):973-9. doi: 10.1111/1346-8138.12323. Epub 2013 Dec 4.

Abstract

S100P is a member of the S100 family. Increased levels of S100P have been documented in various malignancies. Binding of extracellular S100P to receptor for advanced glycation end products (RAGE) or coupling of intracellular S100P with a cytoskeletal protein, ezrin, play a crucial role in tumor growth, invasion and metastasis. However, little is known about the expression of S100P, RAGE and ezrin in malignant melanoma. We immunostained these three molecules in 20 primary and 20 metastatic melanomas. Samples of 20 benign nevus pigmentosus and 10 of normal skin were tested as controls. The expression levels (percentage of positively stained cells) of S100P, RAGE and ezrin were significantly higher in melanomas than in nevus pigmentosus. Moreover, slightly but significantly higher expression levels were observed in metastatic than in primary melanomas. Significant positive correlations were evident between the expression levels of S100P and RAGE, S100P and ezrin, and RAGE and ezrin, respectively. In conclusion, the coordinate upregulation of S100P, RAGE and ezrin may possibly facilitate malignant transformation of melanoma.

摘要

S100P 是 S100 家族的一员。已经有文献记录表明,S100P 在各种恶性肿瘤中表达水平升高。细胞外 S100P 与晚期糖基化终产物受体(RAGE)结合,或细胞内 S100P 与细胞骨架蛋白 ezrin 偶联,在肿瘤生长、侵袭和转移中发挥关键作用。然而,S100P、RAGE 和 ezrin 在恶性黑色素瘤中的表达情况知之甚少。我们对 20 例原发性和 20 例转移性黑色素瘤中的这三种分子进行了免疫染色。以 20 例良性色素痣和 10 例正常皮肤作为对照进行了检测。S100P、RAGE 和 ezrin 的表达水平(阳性染色细胞的百分比)在黑色素瘤中明显高于色素痣。此外,转移性黑色素瘤的表达水平略高于原发性黑色素瘤。S100P 和 RAGE、S100P 和 ezrin、RAGE 和 ezrin 之间的表达水平分别存在显著的正相关关系。总之,S100P、RAGE 和 ezrin 的协调上调可能有助于黑色素瘤的恶性转化。

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