Increased ALK1 copy number and renal cell carcinoma - A case report

Ciara Ryan, Nick Mayer, Joan Cunningham, Gordon Hislop, Norman Pratt, Stewart Fleming (Lead / Corresponding author)

    Research output: Contribution to journalArticlepeer-review

    15 Citations (Scopus)


    There have been recent reports of a rare variant of renal cell carcinoma associated with upregulation of the anaplastic lymphoma kinase gene (ALK) arising as a consequence of chromosomal translocations. The tumours were described as having a characteristic morphology. Here, we describe a case with similar morphology characterised by eosinophilic cells, abundant intracytoplasmic lumina and scattered large ganglion-like tumour cells. There was focal staining for ALK demonstrated by immunohistochemistry. However, rather than exhibiting a chromosomal translocation involving ALK, the use of FISH and a break-apart probe demonstrated that there was increased copy number of intact 2p23, the chromosomal region containing the ALK gene. Furthermore, the use of comparative genomic hybridisation showed increase of the whole of chromosome 2 along with chromosomes 6 and 17. There was no evidence of loss of 3p nor of trisomy of 7 associated with clear cell and papillary carcinoma, respectively. We suggest that this demonstrates a novel mechanism of upregulation of ALK activity by increased copy number occurring during the development of a renal carcinoma with the characteristic ALK-associated morphology.

    Original languageEnglish
    Pages (from-to)241-245
    Number of pages5
    JournalVirchows Archiv
    Issue number2
    Publication statusPublished - Feb 2014


    • ALK
    • Copy number
    • Renal cell carcinoma

    ASJC Scopus subject areas

    • Pathology and Forensic Medicine
    • Molecular Biology
    • Cell Biology


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