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The in vivo modulatory effects of an anterior-chamber microenvironment on uveal melanoma.
- Source :
-
The British journal of ophthalmology [Br J Ophthalmol] 2009 Apr; Vol. 93 (4), pp. 535-40. Date of Electronic Publication: 2008 Nov 19. - Publication Year :
- 2009
-
Abstract
- Background: Primary melanoma of the iris, for reasons unknown has a lower metastatic rate compared with primary ciliary-body melanoma. Six histology cases of ciliary-body melanoma were identified that had spread onto the iris surface and into the stroma, representing a change in tumour microenvironment from aqueous humour non-exposure (ciliary-body component) to aqueous humour exposure (iris surface component). This provided an ideal paradigm for investigating the effects of different environments on melanoma.<br />Method: Conventional light microscopy was performed on stained paraffin sections of the identified cases, followed by immunohistochemistry to cell cycle proteins p27 and Cyclin D1. Fluorescence in situ hybridisation (FISH) analysis was conducted on the paraffin sections for changes of chromosomes 3 and 8, associated with poor uveal melanoma prognosis.<br />Results: Iris surface melanoma cells were smaller compared with the adjacent deeper iris stromal melanoma cells and with those in the ciliary body. Fewer iris surface melanoma cells expressed Cyclin D1 protein, but more expressed p27 protein, compared with the larger iris stromal melanoma cells (paired Wilcoxon signed ranks test: Cyclin D1 p = 0.028; p27 p = 0.046) and with the ciliary-body melanoma cells (paired Wilcoxon signed ranks test: Cyclin D1 p = 0.028; p27 p = 0.028). With FISH, chromosome 3 and 8 alterations were less common among the iris surface melanoma cells than the deeper iris stromal melanoma cells and the ciliary-body melanoma cells, which were consistently characterised by a relative genetic imbalance for chromosomes 3 and 8.<br />Conclusions: These data suggest that there are tumour-modulatory factors within the anterior chamber environment that probably select populations of ciliary-body melanoma cells, with a less aggressive, better-differentiated status. Furthermore, it may help explain why iris melanomas generally have a less aggressive course than ciliary-body and choroidal melanomas.
- Subjects :
- Aged
Aged, 80 and over
Chromosomes, Human, Pair 3 genetics
Chromosomes, Human, Pair 8 genetics
Cyclin D1 metabolism
Female
Humans
In Situ Hybridization, Fluorescence methods
Iris pathology
Male
Melanoma genetics
Melanoma metabolism
Middle Aged
Neoplasm Invasiveness
Neoplasm Proteins metabolism
Proliferating Cell Nuclear Antigen metabolism
Tissue Fixation methods
Uveal Neoplasms genetics
Uveal Neoplasms metabolism
Anterior Chamber physiopathology
Ciliary Body
Melanoma pathology
Uveal Neoplasms pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1468-2079
- Volume :
- 93
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- The British journal of ophthalmology
- Publication Type :
- Academic Journal
- Accession number :
- 19019926
- Full Text :
- https://doi.org/10.1136/bjo.2008.147314