Literature DB >> 17696912

Predominant formation of heavily pigmented dermal melanocytomas resembling 'animal-type' melanomas in hepatocyte growth factor (C57BL/6 x C3H)F1 mice following neonatal UV irradiation.

Scott R Florell1, Joshua Thomas, Douglas Grossman.   

Abstract

BACKGROUND: Transgenic mice expressing hepatocyte growth factor (HGF) develop cutaneous melanocytic tumors following neonatal UV exposure. Here, we examined the histologic spectrum of UV-induced melanocytic tumors in HGF mice on a pigmented (C57BL/6 x C3H/HeN)F(1) background.
METHODS: Neonatally irradiated (4000 J/m(2)) mice were monitored for 43 weeks, and 31/34 (91%) animals developed a total of 163 melanocytic tumors.
RESULTS: Of 54 primary tumors analyzed, most (49/54, 91%) demonstrated exclusively dermal collections of epithelioid cells with voluminous densely pigmented cytoplasm. Seven of these also demonstrated a population of spindled cells with mitoses. Several (3/54, 6%) tumors exhibited a junctional component with melanocytes present in the epidermis. Staining with PEP8 confirmed the presence of interfollicular melanocytes at the dermal-epidermal junction in neonatal skin.
CONCLUSIONS: In contrast to HGF animals on an albino (FVB) background, HGF animals on the pigmented (C57BL/6 x C3H/HeN)F(1) background do not develop classic radial growth phase melanoma but rather predominantly develop dermal melanocytomas resembling the 'animal-type' melanoma occasionally seen in humans. These results demonstrate the influence of genetic background on histologic pattern of UV-induced melanomas in mice.

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Year:  2007        PMID: 17696912      PMCID: PMC2410209          DOI: 10.1111/j.1600-0560.2006.00679.x

Source DB:  PubMed          Journal:  J Cutan Pathol        ISSN: 0303-6987            Impact factor:   1.587


  37 in total

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3.  Ink4a/arf deficiency promotes ultraviolet radiation-induced melanomagenesis.

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4.  Neonatal sunburn and melanoma in mice.

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6.  Hepatocyte growth factor and melanoma: gene transfer studies in human melanocytes.

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Review 9.  Animal models of melanoma: an HGF/SF transgenic mouse model may facilitate experimental access to UV initiating events.

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1.  Superficial spreading-like melanoma in Arf(-/-)::Tyr-Nras(Q61K)::K14-Kitl mice: keratinocyte Kit ligand expression sufficient to "translocate" melanomas from dermis to epidermis.

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2.  N-acetylcysteine protects melanocytes against oxidative stress/damage and delays onset of ultraviolet-induced melanoma in mice.

Authors:  Murray A Cotter; Joshua Thomas; Pamela Cassidy; Kyle Robinette; Noah Jenkins; Scott R Florell; Sancy Leachman; Wolfram E Samlowski; Douglas Grossman
Journal:  Clin Cancer Res       Date:  2007-10-01       Impact factor: 12.531

3.  NM23 deficiency promotes metastasis in a UV radiation-induced mouse model of human melanoma.

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4.  A murine model for the development of melanocytic nevi and their progression to melanoma.

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  4 in total

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