# Teadenol B as a Component of Microorganism-Fermented Tea Extract Inhibited Breast Cancers by Promoting Autophagy

**Authors:** Ying Zhao, Zhang-Gui Ding, Yu-Jie Yan, Rui Yang, Miao-Miao Qi, Shu-Kang Pan, Ji-Ling Xie, Yu-Hui Sun, Jin Xiang

PMC · DOI: 10.3390/molecules29040872 · Molecules · 2024-02-16

## TL;DR

Teadenol B, a compound in fermented tea, inhibits breast cancer by promoting autophagy and reducing DNA repair enzymes.

## Contribution

Teadenol B is shown to inhibit all four breast cancer subtypes and promote autophagy, offering a novel therapeutic approach.

## Key findings

- Teadenol B significantly reduced DCTD levels in all four breast cancer cell types.
- Teadenol B suppressed tumor growth in mice without affecting body weight.
- Teadenol B increased LC3-II conversion, indicating autophagy promotion.

## Abstract

Breast cancer is a significant threat to life and health, which needs more safe and effective drugs to be explored. Teadenol B is a characteristic chemical component of microbial fermented tea. This study discovered that teadenol B could exhibit obvious inhibitory effects on all four different clinical subtype characteristics of breast cancer cells. Proteomic studies show that deoxycytidine triphosphate deaminase (DCTD), which could block DNA synthesis and repair DNA damage, had the most significant and consistent reduction in all four types of breast cancer cells with the treatment of teadenol B. Considering MDA-MB-231 cells exhibit poor clinical prognosis and displayed substantial statistical differences in KEGG pathway enrichment analysis results, we investigated its impact on the size and growth of MDA-MB-231 triple-negative breast tumors transplanted into nude mice and demonstrated that teadenol B significantly suppressed tumor growth without affecting body weight significantly. Finally, we found that the conversion of LC3-I to LC3-II in MDA-MB-231 increased significantly with teadenol B treatment. This proved that teadenol B could be a strong autophagy promotor, which explained the down-regulation of DCTD to some extent and may be the potential mechanism underlying teadenol B’s anti-breast cancer effects. This finding provides new evidence for drinking fermented tea to prevent breast cancer and highlights the potential of teadenol B as a novel therapeutic option for breast cancer prevention and treatment, necessitating further investigations to clarify its exact target and the details involved.

## Linked entities

- **Proteins:** DCTD (dCMP deaminase), Map1lc3a (microtubule-associated protein 1 light chain 3 alpha), Map1lc3a (microtubule-associated protein 1 light chain 3 alpha)
- **Chemicals:** Teadenol B (PubChem CID 68196394)
- **Diseases:** breast cancer (MONDO:0004989)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** DCTD (dCMP deaminase) [NCBI Gene 1635], MAP1LC3A (microtubule associated protein 1 light chain 3 alpha) [NCBI Gene 84557] {aka ATG8E, LC3, LC3A, MAP1ALC3, MAP1BLC3}
- **Diseases:** tumor (MESH:D009369), Breast Cancers (MESH:D001943)
- **Chemicals:** Fermented Tea (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** MDA-MB-231 — Homo sapiens (Human), Breast adenocarcinoma, Cancer cell line (CVCL_0062)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC10892666/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10892666/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC10892666/full.md

---
Source: https://tomesphere.com/paper/PMC10892666