# Circaea mollis Siebold & Zucc. Induces Apoptosis in Colorectal Cancer Cells by Inhibiting c-Myc Through the Mediation of RPL5

**Authors:** So-Mi Park, Nanyeong Kim, Ye-Rin Park, Seok Woo Kim, Ji Hoon Jung, Yun-Cheol Na, Daeho Kwon, Hyungsuk Kim, Hyeung-Jin Jang

PMC · DOI: 10.3390/ijms26104664 · International Journal of Molecular Sciences · 2025-05-13

## TL;DR

A traditional plant called Circaea mollis shows potential in fighting colorectal cancer by reducing a harmful protein called c-Myc.

## Contribution

This study reveals that Circaea mollis induces apoptosis in colorectal cancer cells by inhibiting c-Myc via RPL5 mediation.

## Key findings

- CS&Z induces apoptosis and G1/S phase cell cycle arrest in colorectal cancer cells.
- CS&Z suppresses c-Myc, and this effect is reversed by RPL5 depletion.
- CS&Z synergizes with doxorubicin and 5-fluorouracil in treating colorectal cancer.

## Abstract

Colorectal cancer remains a significant global health concern. In this study, we investigated the anticancer potential of Circaea mollis Siebold & Zucc. (CS&Z), a traditional medicinal plant known for its anti-inflammatory, anti-arthritic, and antioxidant properties, in the treatment of colorectal cancer. We found that CS&Z induces apoptosis and G1/S phase cell cycle arrest in colorectal cancer cells, primarily through the suppression of the proto-oncogene c-Myc. Specifically, the depletion of RPL5, a ribosomal protein associated with c-Myc regulation, reversed the suppression of c-Myc by CS&Z. Additionally, when co-administered with the standard chemotherapeutic agents doxorubicin and 5-fluorouracil, CS&Z demonstrated synergistic effects, thereby further emphasizing its potential efficacy as a therapeutic option for the treatment of colorectal cancer. Moreover, the constituents of CS&Z, detected through liquid chromatography–mass spectrometry analysis, reportedly exhibit anticancer activities. Taken together, our findings suggest that CS&Z holds promise as a natural product capable of modulating oncogenic signaling in colorectal cancer and may serve as a complementary agent in future therapeutic strategies.

## Linked entities

- **Genes:** MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 4609], RPL5 (ribosomal protein L5) [NCBI Gene 6125]
- **Chemicals:** doxorubicin (PubChem CID 31703), 5-fluorouracil (PubChem CID 3385)
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 4609] {aka MRTL, MYCC, bHLHe39, c-Myc}, RPL5 (ribosomal protein L5) [NCBI Gene 6125] {aka L5, MSTP030, PPP1R135, uL18}
- **Diseases:** Colorectal Cancer (MESH:D015179), inflammatory (MESH:D007249), arthritic (MESH:D015535)
- **Chemicals:** 5-fluorouracil (MESH:D005472), doxorubicin (MESH:D004317)
- **Species:** Circaea mollis (species) [taxon 658105]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12111350/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12111350/full.md

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Source: https://tomesphere.com/paper/PMC12111350