In vivo human melanoma cytokine production: Inverse correlation of GM-CSF production with tumor depth

被引:16
作者
Hensley, C
Spitzler, S
McAlpine, BE
Lynn, M
Ansel, JC
Solomon, AR
Armstrong, CA
机构
[1] Emory Univ, Sch Med, Dept Dermatol, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Winship Canc Ctr, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Dept Pathol, Atlanta, GA 30322 USA
[4] Vet Affairs Med Ctr, Serv Dermatol, Atlanta, GA 30033 USA
[5] Emory Univ, Sch Publ Hlth, Dept Biostat, Atlanta, GA 30322 USA
关键词
melanoma; granulocyte macrophage; colony stimulating factor (GM-CSF); interleukin-8 (IL-8); tumor thickness;
D O I
10.1111/j.1600-0625.1998.tb00333.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
Melanomas produce multiple cytokines which may influence their growth in vivo. Experimental evidence suggests that granulocyte macrophage-colony stimulating factor (GM-CSF) can induce a potent anti-melanoma response, whereas interleukin-8 (IL-8) may act as a growth factor in human melanoma. Little is currently known regarding the production of these cytokines by human melanoma in vivo. In this study we tested the hypothesis that endogenous production of GM-CSF and IL-8 can be correlated with the depth of human malignant melanoma surgical specimens. We examined 45 melanocytic human tissue samples consisting of 27 primary cutaneous melanomas, 9 metastatic melanomas, and 9 dysplastic nevi for in viva GM-CSF and IL-8 production using immunohistochemistry. The majority of thin melanomas (less than or equal to 0.76 mm) stained highly positive for GM-CSF with little or no staining for IL-8 whereas the medium (>0.76-less than or equal to 4.0 mm) and thick (>4.0 mm) melanoma specimens showed little or no staining for GM-CSF and significant amounts of IL-8 staining. Metastatic melanoma as well as dysplastic nevi specimens had little or no GM-CSF and IL-8 staining. These results support the hypothesis that endogenous melanoma cytokines such as GM-CSF and IL-8 with opposing effects on turner progression play an important role in melanoma growth and regulation.
引用
收藏
页码:335 / 341
页数:7
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