Varney Michelle L, Johansson Sonny L, Singh Rakesh K
Department of Pathology and Microbiology, the University of Nebraska Medical Center, Omaha 68198-5845, USA.
Am J Clin Pathol. 2006 Feb;125(2):209-16. doi: 10.1309/VPL5-R3JR-7F1D-6V03.
We examined the expression of CXCL8 (interleukin-8), its receptors, CXCR1 and CXCR2, and vessel density in human melanoma by immunohistochemical analysis of tumors from different Clark levels, depths, and thicknesses. Expression of CXCL8 and CXCR2 was lower in Clark level I and II specimens than in level III through V specimens and metastases. CXCR1 expression was observed ubiquitously in the majority of human melanoma tumor specimens irrespective of disease state, with the highest intensity in Clark level III specimens. We observed a significant difference in CXCL8 and CXCR2 expression between thin (<or=0.75 mm) and thick (>0.75 mm) melanomas and between thin and metastatic lesions. Positive correlations were observed between Clark level and CXCL8 or CXCR2 and between thickness and CXCR2 expression. We found no correlation between vessel density and Clark level or thickness. Our data suggest that expression of CXCL8 and CXCR2 contributes to aggressive growth and metastasis in human malignant melanoma. Consistent with the transition from radial to vertical growth phase melanoma, expression of CXCL8 and its receptor, CXCR2, may be key in the switch to an aggressive, more metastatic phenotype.
我们通过对来自不同Clark分级、深度和厚度的人类黑色素瘤肿瘤进行免疫组织化学分析,检测了CXCL8(白细胞介素-8)及其受体CXCR1和CXCR2的表达以及血管密度。CXCL8和CXCR2在Clark I级和II级标本中的表达低于III级至V级标本及转移灶。无论疾病状态如何,在大多数人类黑色素瘤肿瘤标本中均普遍观察到CXCR1表达,在Clark III级标本中表达强度最高。我们观察到薄型(≤0.75 mm)和厚型(>0.75 mm)黑色素瘤之间以及薄型病变与转移灶之间CXCL8和CXCR2表达存在显著差异。在Clark分级与CXCL8或CXCR2之间以及厚度与CXCR2表达之间观察到正相关。我们发现血管密度与Clark分级或厚度之间无相关性。我们的数据表明,CXCL8和CXCR2的表达有助于人类恶性黑色素瘤的侵袭性生长和转移。与黑色素瘤从放射状生长阶段向垂直生长阶段的转变一致,CXCL8及其受体CXCR2的表达可能是转变为侵袭性更强、更具转移性表型的关键。