A2780

Cat.No.: CSC-C9491J

Species: Homo sapiens (Human)

Source: Ovary

Morphology: Epithelial

Culture Properties: Adherent

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Cat.No.
CSC-C9491J
Description
The A2780 human ovarian cancer cell line was established from tumour tissue from an untreated patient. Cells grow as a monolayer and in suspension in spinner cultures. A2780 is the parent line to the cisplatin resistant cell line A2780 cis and the adriamycin resistant cell line A2780 ADR.
Species
Homo sapiens (Human)
Source
Ovary
Recommended Medium
RPMI 1640 + 2mM Glutamine + 10% Fetal Bovine Serum (FBS)
Culture Properties
Adherent
Morphology
Epithelial
Disease
Ovarian Endometrioid Adenocarcinoma
Storage
Creative Bioarray ships frozen cells on dry ice. On receipt, immediately transfer frozen cells to liquid nitrogen (-180 °C) until ready for experimental use.
Never can cryopreserved cells be kept at -20 °C.
Synonyms
A-2780; 2780; A2780S; A2780par
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.

A2780 is a human ovarian endometrioid adenocarcinoma cell line, originally established in 1972 from an untreated patient with advanced-stage disease. Its singular scientific advantage resides in its status as the chemotherapy-sensitive parental archetype for isogenic drug resistance research. Unlike heterogeneous patient samples, A2780 provides a pure, syngeneic background against which resistance mechanisms can be experimentally isolated.

The line's power lies in its derivative platform. Chronic exposure of A2780 to cisplatin and adriamycin has generated the widely adopted resistant sublines A2780cis and A2780ADR, which exhibit cross-resistance to melphalan, vinblastine, and irradiation. This matched pair enables precise dissection of ATP-binding cassette (ABC) transporter efflux (MDR1/BCRP), EMT programming (VIM, SNAIL1/2), and ECM-mediated chemoprotection-mechanisms often confounded in non-isogenic comparisons.

Genomically, A2780 harbors clinically relevant driver mutations in TP53, BRCA1, PTEN (homozygous deletion), PIK3CA, and ATM. It retains stable, authenticated STR profiles and forms tumors in nude mice, bridging monolayer screening and in vivo efficacy. Critically, A2780 is exquisitely amenable to 3D multicellular spheroid culture, a configuration that recapitulates solid tumor hypoxia, G0-G1 cell cycle arrest, and p27-mediated chemoresistance-features lost in 2D.

Zein-Sodium Caseinate-Diosmin Nanoparticles as A Promising Anti-Cancer Agent with Targeted Efficacy Against A2780 Cell Line

This research investigated the potential of zein-sodium caseinate-diosmin nanoparticles (ZCD-NPs) as an anti-cancer agent against the A2780 cell line. Dynamic light scattering (DLS) analysis showed that ZCD-NPs have an average size of 265.30 nm with a polydispersity index of 0.21, indicating good uniformity suitable for pharmaceutical applications. Cytotoxicity assays showed a dose-dependent effect of ZCD-NPs, with A2780 cells showing significant sensitivity compared to normal HDF cells, indicating selective targeting of cancer cells. Flow cytometry analysis confirmed that ZCD-NPs induced apoptosis and necrosis in A2780 cells, as evidenced by increased expression of apoptotic genes such as p53 and caspases 8 and 9. In addition, ZCD-NPs exhibited potent antioxidant activity, effectively scavenging free radicals. These results suggest that ZCD-NPs have promising properties for targeted cancer therapy and antioxidant applications, which warrant further exploration in clinical settings.

Flow cytometry results indicate that ZCD-NPs induce apoptosis in A2780 cells in a concentration-dependent manner, with significant increases in apoptotic rates at higher concentrations.

Fig. 1. Flow cytometry results indicate that ZCD-NPs induce apoptosis in A2780 cells in a concentration-dependent manner (Faezi, Mahmoud, et al., 2025).

AO/PI staining analyses show that ZCD-NPs induce significant cytotoxic effects in A2780 cells, as evidenced by decreased green and increased red. DAPI staining further confirms a dose-dependent increase in nuclear condensation and fragmentation, characteristic of apoptosis.

Fig. 2. Fluorescence graph of A2780 cells stained with AO/PI and DAPI (Faezi, Mahmoud, et al., 2025).

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