Heat shock protein 27 is expressed in normal and malignant human melanocytes in vivo

Background:  Heat shock proteins (HSPs) are a family of highly conserved proteins found ubiquitously in mammalian cells, believed to be regulators of normal cell physiology and the cellular stress response. In addition, the small 27‐kDa heat shock protein (HSP27) has previously been found to be a di...

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Published in:Journal of cutaneous pathology 2004-11, Vol.31 (10), p.665-671
Main Authors: Kang, Steven H., Fung, Maxwell A., Gandour-Edwards, Regina, Reilly, Debra, Dizon, Teresa, Grahn, Jennifer, Isseroff, R. Rivkah
Format: Article
Language:English
Subjects:
Adolescent
Adult
Aged
Aged, 80 and over
Biological and medical sciences
Dermatology
Female
Fluorescent Antibody Technique, Indirect
Heat-Shock Proteins - metabolism
HSP27 Heat-Shock Proteins
Humans
Male
Medical sciences
Melanocytes - metabolism
Melanocytes - pathology
Melanoma - metabolism
Melanoma - pathology
Middle Aged
Neoplasm Proteins - metabolism
Nevus, Intradermal - metabolism
Nevus, Intradermal - pathology
Skin Neoplasms - metabolism
Skin Neoplasms - pathology
Tumor Cells, Cultured
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Summary:Background:  Heat shock proteins (HSPs) are a family of highly conserved proteins found ubiquitously in mammalian cells, believed to be regulators of normal cell physiology and the cellular stress response. In addition, the small 27‐kDa heat shock protein (HSP27) has previously been found to be a differentiation marker for keratinocytes and a prognostic marker associated with increased survival in certain cancerous tumors. Methods:  Using immunohistochemistry on routinely processed paraffin sections, we examined skin biopsies from 15 invasive melanomas, 13 intradermal nevi, and two compound nevi immunostained with a mouse monoclonal antibody to HSP27. In addition, cultured melanocytes were heat stressed at 45°C for 1 h and then fixed and immunostained in order to localize HSP27 expression intracellularly. Results:  We found cytoplasmic and strong perinuclear staining of HSP27 in melanocytes in normal skin, in melanomas, and in nevi. Nuclear reactivity was absent. In addition, in cultured non‐malignant melanocytes, HSP27 expression relocated from the cytoplasm to the nucleus with heat stress. Conclusions:  To our knowledge, this investigation is the first to demonstrate that HSP27 is expressed in melanocytes in normal skin, in nevi, and in non‐malignant cultured melanocytes.
ISSN:0303-6987
1600-0560
DOI:10.1111/j.0303-6987.2004.00248.x