Unknown

Dataset Information

0

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


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.

SUBMITTER: Hoggarth ZE 

PROVIDER: S-EPMC6724223 | biostudies-literature | 2019 Jul

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC6294394 | biostudies-literature
| S-EPMC4718619 | biostudies-literature
| S-EPMC10252886 | biostudies-literature
| S-EPMC9775150 | biostudies-literature
| S-EPMC4536367 | biostudies-literature
| S-EPMC6060623 | biostudies-literature
| S-EPMC7227614 | biostudies-literature
| S-EPMC1392234 | biostudies-literature
2019-01-01 | GSE110694 | GEO
| S-EPMC7500507 | biostudies-literature