| Literature DB >> 26916071 |
Alka Mahale1, Hind Alkatan2, Saeed Alwadani1,2,3, Maha Othman1, Maria J Suarez3, Antoinette Price4, Hailah Al-Hussain1, Sabah Jastaneiah1, Wayne Yu5, Azza Maktabi1, Edward P Deepak1,3, Charles G Eberhart3,4,6, Laura Asnaghi4.
Abstract
Conjunctival squamous cell carcinoma is a malignancy of the ocular surface. The molecular drivers responsible for the development and progression of this disease are not well understood. We therefore compared the transcriptional profiles of eight snap-frozen conjunctival squamous cell carcinomas and one in situ lesion with normal conjunctival specimens in order to identify diagnostic markers or therapeutic targets. RNA was analyzed using oligonucleotide microarrays, and a wide range of transcripts with altered expression identified, including many dysregulated in carcinomas arising at other sites. Among the upregulated genes, we observed more than 30-fold induction of the matrix metalloproteinases, MMP-9 and MMP-11, as well as a prominent increase in the mRNA level of a calcium-binding protein important for the intracellular calcium signaling, S100A2, which was induced over 20-fold in the tumor cohort. Clusterin was the most downregulated gene, with an approximately 180-fold reduction in the mRNA expression. These alterations were all confirmed by qPCR in the samples used for initial microarray analysis. In addition, immunohistochemical analysis confirmed the overexpression of MMP-11 and S100A2, as well as reductions in clusterin, in several independent in situ carcinomas of conjunctiva. These data identify a number of alterations, including upregulation of MMP-9, MMP-11, and S100A2, as well as downregulation of clusterin, associated with epithelial tumorigenesis in the ocular surface.Entities:
Mesh:
Year: 2016 PMID: 26916071 DOI: 10.1038/modpathol.2016.41
Source DB: PubMed Journal: Mod Pathol ISSN: 0893-3952 Impact factor: 7.842