# 2-methoxyestradiol inhibits the malignant behavior of triple negative breast cancer cells by altering their miRNome

**Authors:** Ramadevi Subramani, Animesh Chatterjee, Diego A. Pedroza, Seeta Poudel, Preetha Rajkumar, Jeffrey Annabi, Elizabeth Penner, Rajkumar Lakshmanaswamy

PMC · DOI: 10.3389/fonc.2024.1371792 · 2024-09-12

## TL;DR

This study shows that 2-methoxyestradiol (2ME2) can inhibit the growth and spread of triple-negative breast cancer cells by altering their miRNA expression.

## Contribution

The study demonstrates that 2ME2 alters the miRNome of TNBC cells, impacting cancer-related processes.

## Key findings

- 2ME2 inhibits TNBC cell proliferation and induces apoptosis.
- 2ME2 treatment reduces migration and invasion of TNBC cells.
- 2ME2 alters miRNA expression, affecting genes involved in cancer hallmarks.

## Abstract

Triple-negative breast cancer (TNBC) is a subtype of breast cancer with no effective targeted treatment currently available. Estrogen and its metabolites influence the growth of mammary cancer. Previously, we demonstrated the anti-cancer effects of 2-methoxyestradiol (2ME2) on mammary carcinogenesis.

In the present study, we investigated the effects of 2ME2 on TNBC cells. TNBC (MDA-MB-231 and MDA-MB-468) and non-tumorigenic breast (MCF10A) cell lines were used to determine the effects of 2ME2 on cell proliferation (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium; MTS assay), cell cycle (flow cytometric assay), migration (transwell migration assay), invasion (matrigel invasion assay), apoptosis (annexin V/propidium iodide assay), colony formation (soft agar assay), and miRNome (human miRNA profiling array). The miRNome data were analyzed using the c-BioPortal and Xena platforms. Moreover, Kyoto Encyclopedia of Genes and Genomes, Gene Ontology, and reactome pathway analyses were performed.

We found that 2ME2 effectively inhibited cell proliferation and induced apoptosis. Furthermore, 2ME2 treatment arrested TNBC cells in the S-phase of the cell cycle. Treatment with 2ME2 also significantly decreased the aggressiveness of TNBC cells by inhibiting their migration and invasion. In addition, 2ME2 altered the miRNA expression in these cells. In silico analysis of the miRNome profile of 2ME2-treated MDA-MB-468 cells revealed that miRNAs altered the target genes involved in many different cancer hallmarks.

2ME2 inhibits triple negative breast cancer by impacting major cellular processes like proliferation, apoptosis, metastasis, etc. It further modifies gene expression by altering the miRNome of triple negative breast cancer cells. Overall, our findings suggest 2ME2 as a potent anti-cancer drug for the treatment of TNBC.

## Linked entities

- **Chemicals:** 2-methoxyestradiol (PubChem CID 66414)
- **Diseases:** triple-negative breast cancer (MONDO:0005494)

## Full-text entities

- **Genes:** ANXA5 (annexin A5) [NCBI Gene 308] {aka ANX5, CPB-I, ENX2, HEL-S-7, PP4, RPRGL3}
- **Diseases:** mammary carcinogenesis (MESH:D063646), metastasis (MESH:D009362), TNBC (MESH:D064726), breast cancer (MESH:D001943), cancer (MESH:D009369)
- **Chemicals:** propidium iodide (MESH:D011419), 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MESH:C070380), 2-methoxyestradiol (MESH:D000077584)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** MDA-MB-468 — Homo sapiens (Human), Breast adenocarcinoma, Cancer cell line (CVCL_0419), MCF10A — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0598), MDA-MB-231 — Homo sapiens (Human), Breast adenocarcinoma, Cancer cell line (CVCL_0062)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11424607/full.md

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Source: https://tomesphere.com/paper/PMC11424607