IGROV-1

Cat.No.: CSC-C7102J

Species: Homo sapiens (Human)

Source: Ovary

Morphology: Epithelial

Culture Properties: Adherent

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Cat.No.
CSC-C7102J
Description
established from ovary of a 47-year-old female with ovarian endometrioid adenocarcinoma
Species
Homo sapiens (Human)
Source
Ovary
Recommended Medium
RPMI-1640 + 10% FBS
Culture Properties
Adherent
Morphology
Epithelial
Application
Cancer research
Size
1 Frozen Vial
Disease
Ovarian Endometrioid Adenocarcinoma
Storage
Directly and immediately transfer cells from dry ice to liquid nitrogen upon receiving and keep the cells in liquid nitrogen until ready for use.
Shipping
Dry Ice
Restricted Use
For research use only. Not for use in diagnostic procedures.
Quality Control
All cells test negative for mycoplasma, bacteria, yeast, and fungi.
BioSafety Level
BSL-1
Synonyms
Igrov-1; IGROV 1; IGR-OV1; IGROV1; Igrov1; IGR.OV1; IGROV; OV1/P; OV1/p; OV1-P
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

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.

Molecular inhibition of USP14 in cisplatin-sensitive IGROV-1 cells.

Fig. 1. Molecular targeting of USP14 in IGROV-1 cells (Corno, Cristina, et al., 2025).

Computational analysis of the molecular mechanism by which ARN12502 inhibits USP14.

Fig. 2. Contact analysis of the ARN12502-USP14 complex from molecular dynamics (MD) simulations (Corno, Cristina, et al., 2025).

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