Original Article

Subject Category: Melanocytes/Melanoma

Journal of Investigative Dermatology (2007) 127, 2184–2190; doi:10.1038/sj.jid.5700829; published online 26 April 2007

Noninvasive Imaging of Melanoma with Reflectance Mode Confocal Scanning Laser Microscopy in a Murine Model

Daniel S Gareau1,2, Glenn Merlino3, Christopher Corless1,2, Molly Kulesz-Martin1,2 and Steven L Jacques1,2

  1. 1Department of Dermatology, Oregon Health & Science University, Portland, Oregon, USA
  2. 2Department of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA
  3. 3Laboratory of Cell Regulation and Carcinogenesis, National Cancer Institute, Bethesda, Maryland, USA

Correspondence: Dr Daniel S. Gareau, Department of Dermatology, Memorial Sloan Kettering Cancer Center, Dermatology, 160 E. 66th, New York, New York 10022, USA. E-mail: dan@dangareau.net

Received 22 August 2006; Revised 30 January 2007; Accepted 9 February 2007; Published online 26 April 2007.

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Abstract

A reflectance-mode confocal scanning laser microscope (rCSLM) was developed for imaging early-stage melanoma in a living mouse model without the addition of exogenous contrast agents. Lesions were first located by surveying the dorsum with a polarized light camera, then imaged with the rCSLM. The images demonstrated two characteristics of melanoma in this animal model: (1) melanocytes and apparent tumor nests in the epidermis at the stratum spinosum in a state of pagetoid spread and (2) architectural disruption of the dermal–epidermal junction. The epidermal melanocytes and apparent tumor nests had a high melanin content, which caused their reflectance to be fivefold greater than the surrounding epidermis. The rCSLM images illustrate the difference between normal skin and sites with apparent melanoma. This imaging modality shows promise to track the progression of melanoma lesions in animal models.

Abbreviations:

DEJ, epidermal–dermal junction; HGF, hepatocyte growth factor; rCSLM, reflectance-mode confocal scanning laser microscope

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