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      Characterization of Intercalated Cell Markers KIT and LINC01187 in Chromophobe Renal Cell Carcinoma and Other Renal Neoplasms

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          Abstract

          Introduction. Chromophobe renal cell carcinoma (chromophobe RCC) is the third major subcategory of renal tumors after clear cell RCC and papillary RCC, accounting for approximately 5% of all RCC subtypes. Other oncocytic neoplasms seen commonly in surgical pathology practice include the eosinophilic variant of chromophobe RCC, renal oncocytoma, and low-grade oncocytic unclassified RCC. Methods. In our recent next-generation sequencing based study, we nominated a lineage-specific novel biomarker LINC01187 (long intergenic non-protein coding RNA 1187) which was found to be enriched in chromophobe RCC. Like KIT (cluster of differentiation 117; CD117), a clinically utilized chromophobe RCC related biomarker, LINC01187 is expressed in intercalated cells of the nephron. In this follow-up study, we performed KIT immunohistochemistry and LINC01187 RNA in situ hybridization (RNA-ISH) on a cohort of chromophobe RCC and other renal neoplasms, characterized the expression patterns, and quantified the expression signals of the two biomarkers in both primary and metastatic settings. Results. LINC01187, in comparison to KIT, exhibits stronger and more uniform expression within tumors while maintaining temporal and spatial consistency. LINC01187 also is devoid of intra-tumoral heterogeneous expression pattern, a phenomenon commonly noted with KIT. Conclusions. LINC01187 expression can augment the currently utilized KIT assay and help facilitate easy microscopic analyses in routine surgical pathology practice.

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          Most cited references47

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          Is Open Access

          edgeR: a Bioconductor package for differential expression analysis of digital gene expression data

          Summary: It is expected that emerging digital gene expression (DGE) technologies will overtake microarray technologies in the near future for many functional genomics applications. One of the fundamental data analysis tasks, especially for gene expression studies, involves determining whether there is evidence that counts for a transcript or exon are significantly different across experimental conditions. edgeR is a Bioconductor software package for examining differential expression of replicated count data. An overdispersed Poisson model is used to account for both biological and technical variability. Empirical Bayes methods are used to moderate the degree of overdispersion across transcripts, improving the reliability of inference. The methodology can be used even with the most minimal levels of replication, provided at least one phenotype or experimental condition is replicated. The software may have other applications beyond sequencing data, such as proteome peptide count data. Availability: The package is freely available under the LGPL licence from the Bioconductor web site (http://bioconductor.org). Contact: mrobinson@wehi.edu.au
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            Complex heatmaps reveal patterns and correlations in multidimensional genomic data.

            Parallel heatmaps with carefully designed annotation graphics are powerful for efficient visualization of patterns and relationships among high dimensional genomic data. Here we present the ComplexHeatmap package that provides rich functionalities for customizing heatmaps, arranging multiple parallel heatmaps and including user-defined annotation graphics. We demonstrate the power of ComplexHeatmap to easily reveal patterns and correlations among multiple sources of information with four real-world datasets.
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              ggplot2

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                Author and article information

                Contributors
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                Journal
                International Journal of Surgical Pathology
                Int J Surg Pathol
                SAGE Publications
                1066-8969
                1940-2465
                September 2023
                October 16 2022
                September 2023
                : 31
                : 6
                : 1027-1040
                Affiliations
                [1 ]Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA
                [2 ]Michigan Center for Translational Pathology, Ann Arbor, MI, USA
                [3 ]Rogel Cancer Center, Michigan Medicine, Ann Arbor, MI, USA
                [4 ]Howard Hughes Medical Institute, Ann Arbor, MI, USA
                [5 ]Department of Pathology, El Camino Hospital, Mountain View, CA, USA
                [6 ]Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA
                [7 ]Department of Hematology/Oncology, University of Michigan, Ann Arbor, MI, USA
                [8 ]Department of Urology, University of Michigan Medical School, Ann Arbor, MI, USA
                [9 ]Department of Radiation Oncology, University Hospitals Seidman Cancer Center, Case Western Reserve University, Cleveland, OH, USA
                [10 ]Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA
                [11 ]Department of Pathology, The Johns Hopkins Hospital, Baltimore, MD, USA
                Article
                10.1177/10668969221125793
                36250542
                1780fa1e-8855-45a3-848c-2f375853755f
                © 2023

                http://journals.sagepub.com/page/policies/text-and-data-mining-license

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