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鼻窦黑色素瘤中CD44的表达:异构体表达缺失与肿瘤晚期有关吗?

CD44 expression in sinonasal melanomas: is loss of isoform expression associated with advanced tumour stage?

作者信息

Regauer S, Ott A, Berghold A, Beham A

机构信息

Department of Pathology, University of Graz Medical School, Austria.

出版信息

J Pathol. 1999 Jan;187(2):184-90. doi: 10.1002/(SICI)1096-9896(199901)187:2<184::AID-PATH216>3.0.CO;2-2.

Abstract

The expression of the adhesion molecule CD44 was examined in 14 primary sinonasal melanomas (SMs), aggressive neoplasms with short survival times, as CD44 overexpression has been linked to poor survival in human cancers. Immunohistochemistry was performed on formalin-fixed, paraffin-embedded sections with CD44 isoform-specific monoclonal antibodies to the CD44 standard (s) and variant isoforms (v) v5 and v6. CD44s, v5, and v6 were strongly expressed in a membranous pattern in SM in situ, early invasive SM, and in uninvolved respiratory/squamous epithelium. In invasive SM, membranous CD44s expression was identified in a large proportion of melanoma cells. Membranous staining of CD44v5 and v6 was lost in invasive SM, independently of the histological subtype. Diffuse cytoplasmic staining was observed focally in invasive SM and loss of cytoplasmic expression of CD44v6 and v5 was associated with advanced tumour stage in the linear-by-linear association test (p = 0.042 and 0.066, respectively). CD44s may not be important for malignant transformation, as it is expressed in both benign and malignant melanocytes. Loss of membranous CD44 isoform expression in widely invasive SM suggests that loss of cellular adhesion facilitates matrix and vascular infiltration and dissemination of sinonasal melanoma cells.

摘要

在14例原发性鼻窦黑色素瘤(SM)中检测了黏附分子CD44的表达情况,鼻窦黑色素瘤是一种侵袭性肿瘤,患者生存时间较短,因为CD44过表达与人类癌症患者的不良生存情况相关。采用针对CD44标准体(s)以及变异体(v)v5和v6的亚型特异性单克隆抗体,对福尔马林固定、石蜡包埋的切片进行免疫组织化学检测。CD44s、v5和v6在原位SM、早期侵袭性SM以及未受累的呼吸道/鳞状上皮中呈膜性强表达。在侵袭性SM中,大部分黑色素瘤细胞可检测到膜性CD44s表达。侵袭性SM中CD44v5和v6的膜性染色消失,且与组织学亚型无关。在侵袭性SM中局部观察到弥漫性细胞质染色,在线性-线性关联检验中,CD44v6和v5的细胞质表达缺失与肿瘤晚期相关(p值分别为0.042和0.066)。CD44s对恶性转化可能并不重要,因为它在良性和恶性黑素细胞中均有表达。广泛侵袭性SM中膜性CD44亚型表达缺失表明,细胞黏附丧失促进了鼻窦黑色素瘤细胞的基质浸润、血管浸润及扩散。

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