2019
DOI: 10.1007/s12031-019-01318-8
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Identification of Important Invasion-Related Genes in Non-functional Pituitary Adenomas

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Cited by 9 publications
(8 citation statements)
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“…The data showed that invasive tumors preferentially upregulate genes releted to organ morphogenesis, extracellular matrix, and hormone activity, and downregulate those mainly associated with leukocyte chemotaxis, dendrites, and RAGE receptor binding. ESR1, SOX2, TTN, GFAP, WIF1, TTR, XIST, SPAG5, PPBP, AR, IL1R2, and HIST1H1C were found as the top hub genes in the upregulated and downregulated networks [172]. Immunohistochemical validation of the expression of putative biomarkers of invasion previously suggested by gene expression profiling studies is still limited.…”
Section: Pathological and Molecular Considerationsmentioning
confidence: 96%
See 1 more Smart Citation
“…The data showed that invasive tumors preferentially upregulate genes releted to organ morphogenesis, extracellular matrix, and hormone activity, and downregulate those mainly associated with leukocyte chemotaxis, dendrites, and RAGE receptor binding. ESR1, SOX2, TTN, GFAP, WIF1, TTR, XIST, SPAG5, PPBP, AR, IL1R2, and HIST1H1C were found as the top hub genes in the upregulated and downregulated networks [172]. Immunohistochemical validation of the expression of putative biomarkers of invasion previously suggested by gene expression profiling studies is still limited.…”
Section: Pathological and Molecular Considerationsmentioning
confidence: 96%
“…Specifically, they found six genes which appeared to be novel molecular biomarkers for invasion, which may be useful for diagnostic purposes: claudin 7 (CLDN7), contactin associated protein-like 2 (CNTNAP2), integrin, α6 (ITGA6), junctional adhesion molecule 3 (JAM3), protein tyrosine phosphatase, receptor type, C (PTPRC), and cadherin-associated protein α1 [171]. Recently, Joshi et al [172] performed molecular screening of genes that are differentially expressed between invasive non-functioning adenoma samples and normal pituitary gland followed by pathway and ontology enrichment analyses. The data showed that invasive tumors preferentially upregulate genes releted to organ morphogenesis, extracellular matrix, and hormone activity, and downregulate those mainly associated with leukocyte chemotaxis, dendrites, and RAGE receptor binding.…”
Section: Pathological and Molecular Considerationsmentioning
confidence: 99%
“…Moreover, previous studies identified a perturbation in some signaling pathways that can make NFPAs prone to invasiveness. The main reported pathways include the “WNT signaling pathway” 12 , “local suppression of the immune response pathway”, “TGF-β signaling” 14 , “PI3K-Akt signaling pathway” and “chemokine signaling pathway” 15 . However, notwithstanding that the molecular markers and pathways associated with NFPA invasiveness are extensively studied, much remains unknown.…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, previous studies identi ed a perturbation in some signaling pathways that can make NFPAs prone to invasiveness. The main reported pathways include the "WNT signaling pathway" [12], "local suppression of the immune response pathway", "TGF-β signaling" [14], "PI3K-Akt signaling pathway" and "chemokine signaling pathway" [15]. However, notwithstanding that the molecular markers and pathways associated with NFPA invasiveness are extensively studied, much remains unknown.…”
Section: Introductionmentioning
confidence: 99%