# Antitumor Compounds From Halophilic Streptomyces violaceorubidus M4 Against Triple‐Negative Breast Cancer

**Authors:** Atousa Zia, Ensieh Salehghamari, Hanieh Jalali, Maryam Taher

PMC · DOI: 10.1002/mbo3.70095 · 2025-10-27

## TL;DR

This study explores a new compound from a salt-loving bacteria that shows promise in fighting a hard-to-treat type of breast cancer.

## Contribution

The discovery of antitumor compounds from Streptomyces violaceorubidus M4 with selective cytotoxicity against triple-negative breast cancer cells.

## Key findings

- The extract showed selective cytotoxicity against MDA-MB-231 cells with an IC50 of 48.04 μg/mL.
- The extract induced apoptosis via the extrinsic pathway, as indicated by changes in Cas-8 and P53 gene expression.
- In mouse models, the extract reduced tumor cell proliferation, mitotic cells, and angiogenesis.

## Abstract

Triple‐negative breast cancer (TNBC) is an aggressive form of breast cancer characterized by the absence of estrogen and progesterone receptors and minimal HER2 expression, restricting the available treatment options. Actinobacteria have emerged as promising sources of anticancer compounds because of their remarkable ability to produce beneficial compounds. This study aimed to evaluate the antitumor effects of the halophilic Streptomyces violaceorubidus M4 extract on TNBC both in vitro and in vivo. The extracted compounds were analyzed by LC‐MS. MTT and annexin‐PI assays were used to assess the apoptosis‐inducing effects of the compounds on MDA‐MB‐231 and MCF‐10A cells. The expression of apoptosis‐related BAX, BCL2, P53, CASPASE‐8, and CASPASE‐9 genes was analyzed using Real‐time PCR. A TNBC mouse model was established using 4T1 cell transplantation, and the animals received the extract intravenously for 21 days. S. violaceorubidus M4 contained bioactive compounds, including amino acids, carboxylic acids, coumarins, isoflavones, phosphatidylcholine, tetrahydroxyanthraquinone, and flavonoids. The extract demonstrated selective cytotoxicity against MDA‐MB‐231 cells, with an IC50 of 48.04 μg/mL after 48 h, while the IC50 for MCF‐10A cells was 132 μg/mL. The reduction in Cas‐9 expression alongside the elevation of Cas‐8 and P53 expression suggests the participation of the extrinsic pathway in the process of apoptosis. Histopathological evaluation of tumor tissues from mouse models showed that the extract injection reduced the number of mitotic cells, nuclear pleomorphism, and angiogenesis in tumor tissue. This study suggests that S. violaceorubidus M4 has a pronounced anticancer effect on TNBC and can be considered for the production of anticancer substances.

The antitumor effects of the halophilic Streptomyces violaceorubidus M4 extract on triple‐negative breast cancer, highlighting its selective cytotoxicity and apoptosis‐inducing properties. Key findings include the identification of bioactive compounds and their impact on apoptosis‐related gene expression, as well as significant reductions in tumor cell proliferation in a mouse model.

## Linked entities

- **Genes:** BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581], BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596], TP53 (tumor protein p53) [NCBI Gene 7157], casp8 (caspase 8, apoptosis-related cysteine peptidase) [NCBI Gene 58022], Casp9 (caspase 9) [NCBI Gene 12371]
- **Chemicals:** coumarins (PubChem CID 54678486), isoflavones (PubChem CID 72304)
- **Diseases:** triple-negative breast cancer (MONDO:0005494), breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, CASP9 (caspase 9) [NCBI Gene 842] {aka APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56}, CASP8 (caspase 8) [NCBI Gene 841] {aka ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5}
- **Diseases:** tumor (MESH:D009369), breast cancer (MESH:D001943), cytotoxicity (MESH:D064420), TNBC (MESH:D064726)
- **Chemicals:** isoflavones (MESH:D007529), annexin-PI (-), coumarins (MESH:D003374), MTT (MESH:C070243), carboxylic acids (MESH:D002264), amino acids (MESH:D000596), flavonoids (MESH:D005419), phosphatidylcholine (MESH:D010713)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** MCF-10A — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0598), 4T1 — Mus musculus (Mouse), Malignant neoplasms of the mouse mammary gland, Cancer cell line (CVCL_0125), MDA-MB-231 — Homo sapiens (Human), Breast adenocarcinoma, Cancer cell line (CVCL_0062)

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12558596/full.md

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Source: https://tomesphere.com/paper/PMC12558596