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Resolution: standard / high Figure 1.
Clinical primary and metastatic melanoma samples procured and cryopreserved at the
time of surgery. A: Intraoperative illustrations of the spectrum of PCM and MM samples procured.
The PCM represents varying tumor thicknesses, measured utilizing Breslow's depth of
invasion. All procured lymph node metastases were macroscopically involved, often
completely replacing the entire lymph node parenchyma. Distant metastatic (subcutaneous
and solid organ) melanoma often exhibited varying degrees of pigmentation, however,
surrounding stroma was avoided in procurement of melanoma samples. B: A distinct change
in the gene expression patterns is apparent within the comparative groups of thin/I.M.
to thick PCM samples. Gene over-expression (upper graph) is evident at the I.M. thickness
sample set, with an average Breslow's tumor thickness of 2.1 mm and 19 mm for thick
melanomas. Contrary, there is a decrease in gene expression (lower graph) of the same
set of genes, with a comparative difference in gene down-regulation evident at the
same interphase of I.M. to thick PCM. Proceeding from left to right: normal skin,
BCC, SCC, MIS, I.M., thick primary, metastatic melanoma (subcutaneous, lymph node
and distant) and melanoma cell lines derived from patients with stage IV melanoma.
Riker et al. BMC Medical Genomics 2008 1:13 doi:10.1186/1755-8794-1-13 |