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CD133+ 细胞含量与慢性阳光损伤皮肤的黑色素瘤中的肿瘤生长相关。

CD133+ cell content correlates with tumour growth in melanomas from skin with chronic sun-induced damage.

机构信息

Experimental Therapeutics and Translational Oncology Program, Instituto de Biología Molecular y Celular del Cáncer, CSIC/Universidad de Salamanca, Campus M. de Unamuno s/n, 37007, Salamanca, Spain; Institute of Biomedical Research of Salamanca (IBSAL), Salamanca, Spain.

出版信息

Br J Dermatol. 2013 Oct;169(4):830-7. doi: 10.1111/bjd.12428.

Abstract

BACKGROUND

Melanoma is responsible for almost 80% of the deaths attributed to skin cancer. Stem cells, defined by CD133 expression, have been implicated in melanoma tumour growth, but their specific role is still uncertain.

OBJECTIVES

We hypothesized that the phenotypic heterogeneity of human cutaneous melanomas is related to their content of CD133+ cells.

METHODS

We compared the percentages of CD133+ cells in 29 tumours from four classic types of melanoma: lentigo maligna melanoma (LMM), superficial spreading melanoma, nodular melanoma and acral lentiginous melanoma (ALM). Also, we compared the percentages of CD133+ cells in melanomas with different degrees of exposure to ultraviolet radiation: 16 melanomas from skin with chronic sun-induced damage and 13 melanomas from skin without such damage.

RESULTS

We found a statistically significant increase of CD133+ cells in three different contexts: in melanomas arising on skin with signs of chronic sun-induced damage vs. nonexposed skin, in melanomas in situ vs. invasive melanomas, and in LMM vs. ALM. The proportions of CD133+ cells did not differ among samples of normal skin with different degrees of sun exposure. A distinct subpopulation of CD133+CXCR4+ cancer stem cells (CSCs) was identified and shown to be related to the invasive phenotype of the tumours.

CONCLUSIONS

Here, we provide evidence showing, for the first time, that an increase in the CD133+ cell content is associated both with melanomas arising on skin with signs of chronic sun-induced damage and in melanomas in situ with better prognosis. Moreover, our study further confirms the existence of a subpopulation of CD133+CXCR4+ CSCs in cutaneous melanomas with invasive phenotype and poor prognosis.

摘要

背景

黑色素瘤是导致皮肤癌死亡的主要原因,占 80%左右。干细胞被定义为 CD133 表达阳性,被认为与黑色素瘤肿瘤的生长有关,但它们的具体作用仍不确定。

目的

我们假设人类皮肤黑色素瘤的表型异质性与其 CD133+细胞含量有关。

方法

我们比较了 29 例来自四种经典黑色素瘤(恶性雀斑样痣黑素瘤、浅表扩散性黑素瘤、结节性黑素瘤和肢端雀斑样黑素瘤)的肿瘤中 CD133+细胞的百分比。此外,我们比较了暴露于不同程度紫外线辐射的黑色素瘤中 CD133+细胞的百分比:16 例来自慢性日光诱导损伤皮肤的黑素瘤和 13 例来自无此类损伤皮肤的黑素瘤。

结果

我们发现了三个不同背景下 CD133+细胞数量的统计学显著增加:在慢性日光诱导损伤皮肤和无暴露皮肤的黑色素瘤中,在原位黑色素瘤与侵袭性黑色素瘤中,以及在恶性雀斑样痣黑素瘤与肢端雀斑样黑素瘤中。不同程度暴露于阳光的正常皮肤样本之间的 CD133+细胞比例没有差异。一个独特的 CD133+CXCR4+癌症干细胞(CSC)亚群被鉴定出来,并显示与肿瘤的侵袭表型有关。

结论

本研究首次提供了证据表明,CD133+细胞含量的增加与慢性日光诱导损伤皮肤的黑色素瘤以及预后较好的原位黑色素瘤的发生有关。此外,我们的研究进一步证实了具有侵袭性表型和不良预后的皮肤黑色素瘤中存在 CD133+CXCR4+CSC 亚群。

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