# Natural Product Epipyrone A from Epicoccum nigrum Exhibits Antiproliferative Activity on Canine Mammary Tumor Cells Through PI3K/Akt/mTOR Pathway Modulation

**Authors:** Consiglia Longobardi, Daria Lotito, Alessia Staropoli, Valeria Iervolino, Nunzio Antonio Cacciola, Serena Montagnaro, Francesco Vinale, Sara Damiano, Roberto Ciarcia

PMC · DOI: 10.3390/antiox15020173 · Antioxidants · 2026-01-28

## TL;DR

A natural compound from a fungus shows promise in fighting dog breast cancer by affecting key cell growth pathways.

## Contribution

Epipyrone A, a fungal metabolite, is identified as a novel antiproliferative agent for canine mammary tumors.

## Key findings

- Epipyrone A reduced cell viability in canine mammary tumor cells in a concentration- and time-dependent manner.
- The compound modulated the PI3K/Akt/mTOR pathway, showing different effects in two cell lines.
- Epipyrone A inhibited cell migration and reduced ROS levels while increasing antioxidant capacity.

## Abstract

Canine mammary tumors (CMTs) are among the most frequent neoplasms in female dogs, with current therapeutic options being limited and non-standardized, prompting the search for alternative treatments such as fungal secondary metabolites. In this study, the fungal pigment Epipyrone A (Epy A) was first isolated from Epicoccum nigrum and then tested in vitro on two CMT cell lines, P114 and CF33. The compound significantly reduced cell viability in both lines in a concentration- and time-dependent manner (p < 0.05), with the strongest effect observed at 175 µg/mL after 48 h (p < 0.0001), while showing no cytotoxicity in MDCK non-tumor cells. Epy A also inhibited cell migration and increased total antioxidant capacity in P114 cells, accompanied by a significant reduction in ROS levels. Western blot analysis revealed modulation of the PI3K/Akt/mTOR pathway, crucial in CMT biology. Specifically, P114 cells showed downregulation of mTOR and p-Akt, indicating inhibition of proliferative signaling, whereas CF33 cells exhibited increased Akt and p-Akt alongside reduced mTOR, consistent with a compensatory feedback mechanism, probably linked to the changing in oxidative balance after treatment. Overall, these results identified Epy A as a promising natural molecule with potential applications in innovative therapeutic approaches for veterinary and comparative oncology.

## Linked entities

- **Proteins:** PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha), AKT1 (AKT serine/threonine kinase 1), MTOR (mechanistic target of rapamycin kinase), Akt (Akt kinase)
- **Species:** Canis lupus familiaris (taxon 9615), Epicoccum nigrum (taxon 105696)

## Full-text entities

- **Genes:** AKT2 (AKT serine/threonine kinase 2) [NCBI Gene 449021], MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 478232] {aka FRAP1}
- **Diseases:** metastasize (MESH:D009362), cytotoxic (MESH:D064420), CMT (MESH:C537989), breast cancer (MESH:D001943), fungal (MESH:D009181), Mammary (MESH:D005348), prostatic cancer (MESH:D011471), injury to (MESH:D014947), anaplastic carcinoma (MESH:D002277), Tumor (MESH:D009369), skin tumours (MESH:D012878), CMTs (MESH:D015674)
- **Chemicals:** penicillin (MESH:D010406), FTY720 (MESH:D000068876), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MESH:C022616), PI (MESH:D011419), ethyl acetate (MESH:C007650), CD3OD (-), epicolactone (MESH:C000634109), epicocconigrone A (MESH:C000608210), MTT (MESH:C070243), CTAB (MESH:D000077286), Na2SO4 (MESH:C012036), agarose (MESH:D012685), purine (MESH:C030985), polyene (MESH:D011090), CO2 (MESH:D002245), DMSO (MESH:D004121), DAPI (MESH:C007293), formazan (MESH:D005562), formic acid (MESH:C030544), Trolox (MESH:C010643), methanol (MESH:D000432), streptomycin (MESH:D013307), Triton X-100 (MESH:D017830), BYL719 (MESH:C585539), ACN (MESH:C032159), EDTA (MESH:D004492), P114 (MESH:C007783), 2',7'-Dichlorofluorescin diacetate (MESH:C029569), H2O (MESH:D014867), 13C (MESH:C000615229), polyketide (MESH:D061065), alkaloids (MESH:D000470), SDS (MESH:D012967), progesterone (MESH:D011374)
- **Species:** Avena sativa (cultivated oat, species) [taxon 4498], Homo sapiens (human, species) [taxon 9606], Canis lupus familiaris (dog, subspecies) [taxon 9615], Avena (genus) [taxon 4496], Human immunodeficiency virus 1 (no rank) [taxon 11676], Epicoccum nigrum (species) [taxon 105696]
- **Mutations:** A from E, H1047R
- **Cell lines:** CMTs — Canis lupus familiaris (Dog), Canine mammary carcinoma, Cancer cell line (CVCL_X218), MDCK — Canis lupus familiaris (Dog), Spontaneously immortalized cell line (CVCL_0422), HEK293 — Homo sapiens (Human), Transformed cell line (CVCL_0045), CMT — Homo sapiens (Human), Charcot-Marie-Tooth neuropathy X type 1, Embryonic stem cell (CVCL_YL11), P114 — Canis lupus familiaris (Dog), Canine mammary carcinoma, Cancer cell line (CVCL_L410), CF33 — Canis lupus familiaris (Dog), Canine mammary carcinoma, Cancer cell line (CVCL_5259), HSCT6 — Rattus norvegicus (Rat), Transformed cell line (CVCL_0315), KA3IT — Homo sapiens (Human), Lung small cell carcinoma, Cancer cell line (CVCL_7023)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938005/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938005/full.md

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Source: https://tomesphere.com/paper/PMC12938005