Enrichment of genes associated with squamous differentiation in cancer initiating cells isolated from urothelial cells transformed by the environmental toxicant arsenite

Arsenic is an environmental toxicant with long-term exposure associated with the development of urothelial carcinomas. Our lab has developed an in-vitro model of urothelial carcinoma by exposing the immortal, but non-tumorigenic bladder cell line, the UROtsa, to arsenite (As3+). These transformed ce...

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Veröffentlicht in:Toxicology and applied pharmacology 2019-07, Vol.374, p.41-52
Hauptverfasser: Hoggarth, Zachary E., Osowski, Danyelle B., Slusser-Nore, Andrea, Shrestha, Swojani, Pathak, Prakash, Solseng, Theoren, Garrett, Scott H., Patel, Divyen H., Savage, Evan, Sens, Donald A., Somji, Seema
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container_title Toxicology and applied pharmacology
container_volume 374
creator Hoggarth, Zachary E.
Osowski, Danyelle B.
Slusser-Nore, Andrea
Shrestha, Swojani
Pathak, Prakash
Solseng, Theoren
Garrett, Scott H.
Patel, Divyen H.
Savage, Evan
Sens, Donald A.
Somji, Seema
description Arsenic is an environmental toxicant with long-term exposure associated with the development of urothelial carcinomas. Our lab has developed an in-vitro model of urothelial carcinoma by exposing the immortal, but non-tumorigenic bladder cell line, the UROtsa, to arsenite (As3+). These transformed cells form tumors in immune-compromised mice, which resemble urothelial carcinomas with components of the tumor exhibiting squamous differentiation. The goal of the present study was to determine the differences in global gene expression patterns between the As3+-transformed UROtsa cells and the urospheres (spheroids containing putative cancer initiating cells) isolated from these cell lines and to determine if the genes involved in the development of squamous differentiation were enriched in the urospheres. The results obtained in this study show an enrichment of genes such as KRT1, KRT5, KRT6A, KRT6B, KRT6C, KRT14 and KRT16 associated with squamous differentiation, a characteristic feature seen in aggressive basal subtypes of urothelial cell carcinoma (UCC) in the urospheres isolated from As3+-transformed UROtsa cells. In addition, there is increased expression of several of the small proline-rich proteins (SPRR) in the urospheres and overexpression of these genes occur in UCC's displaying squamous differentiation. In conclusion, the cancer initiating cells present in the urospheres are enriched with genes associated with squamous differentiation. •UROtsa cells transformed with arsenite show areas of squamous differentiation.•Urospheres are enriched in squamous differentiation and keratinization genes.•There is lack of stability in the urosphere gene expression pattern.•Epigenetic regulation does not play a role in maintaining urosphere gene expression.
doi_str_mv 10.1016/j.taap.2019.04.021
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Our lab has developed an in-vitro model of urothelial carcinoma by exposing the immortal, but non-tumorigenic bladder cell line, the UROtsa, to arsenite (As3+). These transformed cells form tumors in immune-compromised mice, which resemble urothelial carcinomas with components of the tumor exhibiting squamous differentiation. The goal of the present study was to determine the differences in global gene expression patterns between the As3+-transformed UROtsa cells and the urospheres (spheroids containing putative cancer initiating cells) isolated from these cell lines and to determine if the genes involved in the development of squamous differentiation were enriched in the urospheres. The results obtained in this study show an enrichment of genes such as KRT1, KRT5, KRT6A, KRT6B, KRT6C, KRT14 and KRT16 associated with squamous differentiation, a characteristic feature seen in aggressive basal subtypes of urothelial cell carcinoma (UCC) in the urospheres isolated from As3+-transformed UROtsa cells. In addition, there is increased expression of several of the small proline-rich proteins (SPRR) in the urospheres and overexpression of these genes occur in UCC's displaying squamous differentiation. 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Osowski, Danyelle B. ; Slusser-Nore, Andrea ; Shrestha, Swojani ; Pathak, Prakash ; Solseng, Theoren ; Garrett, Scott H. ; Patel, Divyen H. ; Savage, Evan ; Sens, Donald A. ; Somji, Seema</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-7693c2cd6abc209d6974089055fba06010ac4624f67619b09ea6c72e2ca2e50c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Arsenite</topic><topic>Arsenites - toxicity</topic><topic>Biomarkers, Tumor</topic><topic>Cell Line, Tumor</topic><topic>Cell Transformation, Neoplastic - chemically induced</topic><topic>Cluster Analysis</topic><topic>Epigenesis, Genetic</topic><topic>Epithelial Cells - drug effects</topic><topic>Gene Expression Regulation, Neoplastic - drug effects</topic><topic>Humans</topic><topic>Neoplasms, Squamous Cell - metabolism</topic><topic>Protein Array Analysis</topic><topic>Squamous differentiation</topic><topic>Stem cells</topic><topic>Urinary Bladder Neoplasms - metabolism</topic><topic>Urinary Bladder Neoplasms - pathology</topic><topic>Urothelial cell carcinoma</topic><topic>Urothelium - cytology</topic><topic>UROtsa</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoggarth, Zachary E.</creatorcontrib><creatorcontrib>Osowski, Danyelle B.</creatorcontrib><creatorcontrib>Slusser-Nore, Andrea</creatorcontrib><creatorcontrib>Shrestha, Swojani</creatorcontrib><creatorcontrib>Pathak, Prakash</creatorcontrib><creatorcontrib>Solseng, Theoren</creatorcontrib><creatorcontrib>Garrett, Scott H.</creatorcontrib><creatorcontrib>Patel, Divyen H.</creatorcontrib><creatorcontrib>Savage, Evan</creatorcontrib><creatorcontrib>Sens, Donald A.</creatorcontrib><creatorcontrib>Somji, Seema</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Toxicology and applied pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoggarth, Zachary E.</au><au>Osowski, Danyelle B.</au><au>Slusser-Nore, Andrea</au><au>Shrestha, Swojani</au><au>Pathak, Prakash</au><au>Solseng, Theoren</au><au>Garrett, Scott H.</au><au>Patel, Divyen H.</au><au>Savage, Evan</au><au>Sens, Donald A.</au><au>Somji, Seema</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enrichment of genes associated with squamous differentiation in cancer initiating cells isolated from urothelial cells transformed by the environmental toxicant arsenite</atitle><jtitle>Toxicology and applied pharmacology</jtitle><addtitle>Toxicol Appl Pharmacol</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>374</volume><spage>41</spage><epage>52</epage><pages>41-52</pages><issn>0041-008X</issn><eissn>1096-0333</eissn><abstract>Arsenic is an environmental toxicant with long-term exposure associated with the development of urothelial carcinomas. Our lab has developed an in-vitro model of urothelial carcinoma by exposing the immortal, but non-tumorigenic bladder cell line, the UROtsa, to arsenite (As3+). These transformed cells form tumors in immune-compromised mice, which resemble urothelial carcinomas with components of the tumor exhibiting squamous differentiation. The goal of the present study was to determine the differences in global gene expression patterns between the As3+-transformed UROtsa cells and the urospheres (spheroids containing putative cancer initiating cells) isolated from these cell lines and to determine if the genes involved in the development of squamous differentiation were enriched in the urospheres. The results obtained in this study show an enrichment of genes such as KRT1, KRT5, KRT6A, KRT6B, KRT6C, KRT14 and KRT16 associated with squamous differentiation, a characteristic feature seen in aggressive basal subtypes of urothelial cell carcinoma (UCC) in the urospheres isolated from As3+-transformed UROtsa cells. In addition, there is increased expression of several of the small proline-rich proteins (SPRR) in the urospheres and overexpression of these genes occur in UCC's displaying squamous differentiation. In conclusion, the cancer initiating cells present in the urospheres are enriched with genes associated with squamous differentiation. •UROtsa cells transformed with arsenite show areas of squamous differentiation.•Urospheres are enriched in squamous differentiation and keratinization genes.•There is lack of stability in the urosphere gene expression pattern.•Epigenetic regulation does not play a role in maintaining urosphere gene expression.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>31047981</pmid><doi>10.1016/j.taap.2019.04.021</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-8044-5234</orcidid><oa>free_for_read</oa></addata></record>
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subjects Arsenite
Arsenites - toxicity
Biomarkers, Tumor
Cell Line, Tumor
Cell Transformation, Neoplastic - chemically induced
Cluster Analysis
Epigenesis, Genetic
Epithelial Cells - drug effects
Gene Expression Regulation, Neoplastic - drug effects
Humans
Neoplasms, Squamous Cell - metabolism
Protein Array Analysis
Squamous differentiation
Stem cells
Urinary Bladder Neoplasms - metabolism
Urinary Bladder Neoplasms - pathology
Urothelial cell carcinoma
Urothelium - cytology
UROtsa
title Enrichment of genes associated with squamous differentiation in cancer initiating cells isolated from urothelial cells transformed by the environmental toxicant arsenite
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