Data from Metastasizing Melanoma Formation Caused by Expression of Activated N-Ras^Q61K on an INK4a-Deficient Background

Abstract

<div>Abstract<p>In human cutaneous malignant melanoma, a predominance of activated mutations in the N-<i>ras</i> gene has been documented. To obtain a mouse model most closely mimicking the human disease, a transgenic mouse line was generated by targeting expression of dominant-active human N-<i>ras</i> (N-Ras<sup>Q61K</sup>) to the melanocyte lineage by tyrosinase regulatory sequences (Tyr::N-Ras<sup>Q61K</sup>). Transgenic mice show hyperpigmented skin and develop cutaneous metastasizing melanoma. Consistent with the tumor suppressor function of the INK4a locus that encodes p16<sup>INK4A</sup> and p19<sup>ARF</sup>, >90% of Tyr::N-Ras<sup>Q61K</sup> INK4a<sup>−/−</sup> transgenic mice develop melanoma at 6 months. Primary melanoma tumors are melanotic, multifocal, microinvade the epidermis or epithelium of hair follicles, and disseminate as metastases to lymph nodes, lung, and liver. Primary melanoma can be transplanted s.c. in nude mice, and if injected i.v. into NOD/SCID mice colonize the lung. In addition, primary melanomas and metastases contain cells expressing the stem cell marker nestin suggesting a hierarchical structure of the tumors comprised of primitive nestin-expressing precursors and differentiated cells. In conclusion, a novel mouse model with melanotic and metastasizing melanoma was obtained by recapitulating genetic lesions frequently found in human melanoma.</p></div>