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Given this common developmental lineage, Schwann cells may be capable of synthesizing melanin under specific circumstances ( Genetically, MMNST features a complex karyotype with recurring 22q band monosomy, variable whole chromosomal gains, and recurrent losses usually affecting chromosomes 1 and 21 and chromosome arm 17p.45 ( PRKAR1A ) gene ( PRKAR1A gene mutation ( MMNST diagnosis is based on clinical, histopathological, and instrumental findings

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The peptide appears to be permeable into cells, and researchers have suggested selectively inducing senescent cell apoptosis based on results found in studies