IGROV-1
Cat.No.: CSC-C7102J
Species: Homo sapiens (Human)
Source: Ovary
Morphology: Epithelial
Culture Properties: Adherent
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The IGROV-1 cell line is a well-characterized human ovarian adenocarcinoma line, originally established in 1985 from a stage III solid primary tumor of a 47-year-old female patient with no prior chemotherapy treatment. It exhibits an epithelial morphology, adheres as a monolayer in culture, and possesses a doubling time of approximately 20 hours.
A key advantage of the IGROV-1 cell line lies in its distinctive genetic and mutational profile, which uniquely spans both Type I and Type II ovarian cancer signatures. It harbors heterozygous mutations in TP53, BRCA1, PTEN, PIK3CA and ARID1A, and is considered a likely representative of the Type II high-grade serous carcinoma (HGSC) with SET-like morphology. The line is also identified by specific cytogenetic markers, including a paracentric inversion of chromosome 3 and a translocation between chromosomes 2 and 5. Furthermore, it exhibits a hypermutation phenotype, making it an excellent model for genomic instability and DNA damage response research.
From a research application perspective, the IGROV-1 cell line is widely recognized as an established model for drug-resistant ovarian carcinoma. While it retains sensitivity to cisplatin, it demonstrates low to moderate resistance to various other chemotherapeutics, making it an ideal platform for investigating drug resistance mechanisms. Moreover, beyond oncology, it has emerged as a robust in vitro system for virology, with notable susceptibility to SARS-CoV-2 and the ability to mount innate immune responses.
Targeting Deubiquitinase USP14 to Circumvent Cisplatin Resistance in Ovarian Carcinoma
This study aims to investigate the biological role of the proteasome-associated deubiquitinase ubiquitin-specific protease 14 (USP14) in ovarian carcinoma drug resistance and to identify novel USP14 inhibitors (USP14i) for further preclinical development.
Functional studies, including gain- and loss-of-function assays, migration and invasion, and apoptosis induction assays, were conducted using cisplatin-sensitive IGROV-1 cells and their cisplatin-resistant derivative IGROV-1/Pt1. A library of 1,056 small molecules was screened using an optimized hydrolysis assay. Docking and molecular dynamics simulations were employed to predict binding modes of candidate inhibitors within the USP14 domain.
Exogenous overexpression of USP14 enhanced the survival of cisplatin-resistant IGROV-1/Pt1 cells, but not parental IGROV-1 cells, upon cisplatin exposure. USP14 knockdown by small interfering RNAs in resistant cells reduced aggressive features and restored cisplatin sensitivity, whereas no sensitization was observed in IGROV-1 cells. Medium-throughput screening identified five candidate molecules, among which ARN12502 showed the strongest inhibitory activity against USP14. ARN12502 exhibited an IC50 of 18.4 µM, and molecular dynamics simulations confirmed stable binding in two distinct modes.


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