# Repurposing Doxycycline to Overcome High‐Glucose–Induced Mitochondrial Biogenesis–Mediated Chemoresistance in Colorectal Cancer Cells

**Authors:** Chang‐Han Wu, Ching‐Wen Huang, Yen‐Cheng Chen, Kwan‐Ling Yip, Zhi‐Feng Miao, Wei‐Chih Su, Tsung‐Kun Chang, Hsiang‐Lin Tsai, Yung‐Sung Yeh, Hsiao‐Sheng Liu, Jaw‐Yuan Wang

PMC · DOI: 10.1111/jcmm.70795 · Journal of Cellular and Molecular Medicine · 2025-10-13

## TL;DR

High glucose increases chemoresistance in colorectal cancer, but doxycycline can help overcome this resistance by targeting mitochondrial biogenesis.

## Contribution

Repurposing doxycycline to counteract high-glucose-induced chemoresistance in colorectal cancer.

## Key findings

- High glucose increases mitochondrial mass and chemoresistance in CRC cells.
- Doxycycline reduces mitochondrial biogenesis and chemoresistance in hyperglycaemic CRC models.

## Abstract

Chemoresistance is a major contributor to treatment failure in most patients with cancer. Hyperglycaemia enhances chemoresistance in stage III colorectal cancer (CRC) patients, potentially through a mechanism involving c‐Myc. Phospho‐PGC‐1α (p‐PGC‐1α), a transcription coactivator, regulates energy metabolism with c‐Myc and is a key regulator of mitochondrial biogenesis. We hypothesised that high glucose (HG) promotes mitochondrial biogenesis by upregulating c‐Myc and p‐PGC‐1α, thus enhancing chemoresistance in CRC cells, and that inhibiting mitochondrial biogenesis alleviates this chemoresistance. In vitro, HG significantly increased mitochondrial mass (p < 0.001), oxygen consumption rate (p < 0.001), cell migration (p < 0.05) and oxaliplatin resistance (p < 0.001) in LoVo and HCT116 cells. p‐PGC‐1α and COX4 protein expression were increased in the HG and oxaliplatin‐resistance groups in LoVo and HCT116 cells (all p < 0.001) and decreased in the doxycycline group (p < 0.001). In vivo, doxycycline combined with oxaliplatin more notably reduced tumour volume than oxaliplatin alone in hyperglycaemic BALB/c nude mice (p < 0.05). c‐Myc, p‐PGC‐1α and COX4 protein expression were significantly higher in tissues with CRC and hyperglycaemia who experienced relapse than in those with CRC and normoglycaemia who did not experience relapse (all p < 0.05). Overall, this study demonstrated that HG upregulates p‐PGC‐1α and COX4 expression to enhance oxaliplatin resistance by promoting mitochondrial biogenesis and indicates that doxycycline can overcome the chemoresistance induced by HG. Repurposing of doxycycline might reduce chemoresistance in hyperglycaemic CRC patients receiving adjuvant chemotherapy.

## Linked entities

- **Genes:** MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 4609], PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891], COX4I1 (cytochrome c oxidase subunit 4I1) [NCBI Gene 1327]
- **Proteins:** COX4I1 (cytochrome c oxidase subunit 4I1)
- **Chemicals:** doxycycline (PubChem CID 54671203), oxaliplatin (PubChem CID 9887053)
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** COX4I1 (cytochrome c oxidase subunit 4I1) [NCBI Gene 1327] {aka COX IV-1, COX4, COX4-1, COXIV, COXIV-1, MC4DN16}, MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 4609] {aka MRTL, MYCC, bHLHe39, c-Myc}, PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891] {aka LEM6, PGC-1(alpha), PGC-1alpha, PGC-1v, PGC1, PGC1A}
- **Diseases:** CRC (MESH:D015179), cancer (MESH:D009369)
- **Chemicals:** glucose (MESH:D005947), High-Glucose (-), Doxycycline (MESH:D004318), oxygen (MESH:D010100), oxaliplatin (MESH:D000077150)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** LoVo — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0399), HCT116 — Homo sapiens (Human), Colon carcinoma, Cancer cell line (CVCL_0291)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12516229/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12516229/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12516229/full.md

---
Source: https://tomesphere.com/paper/PMC12516229