# Factors associated with clinical outcomes of breast cancer based on glucose metabolic activity of subcutaneous adipose tissue

**Authors:** Jinci Mai, Huanhua Wu, Wanwan Wu, Jinjun Zhou, Yuee Wu, Xiaobei Duan, Rizhao Wu, Youzhu Hu, Zuowu Zhen, Binhao Huang

PMC · DOI: 10.3389/fonc.2026.1722085 · Frontiers in Oncology · 2026-02-23

## TL;DR

This study shows that glucose metabolic activity in subcutaneous fat is linked to worse outcomes in breast cancer patients.

## Contribution

The study introduces SUVmean_SAT as a novel independent prognostic factor for breast cancer progression.

## Key findings

- SUVmean_SAT and AJCC stage are significant independent prognostic factors for breast cancer.
- Combining SUVmean_SAT with AJCC stage improves predictive accuracy for progression-free survival.
- High SUVmean_SAT is associated with increased risk of cancer progression.

## Abstract

Obesity increases the risk of breast cancer, with dysfunctional metabolic activity in subcutaneous adipose tissue (SAT) implicated as a key underlying mechanism. This study sought to explore the correlation between SAT metabolic activity and clinical prognosis among patients with breast cancer.

Body composition parameters at the level of the third lumbar vertebra and clinicopathological data from 74 patients with breast cancer were collected. Two Cox models were established using the least absolute shrinkage and selection operator (LASSO) for variable selection. The two models were compared using the time-dependent area under the receiver operating characteristic curve (AUC) and the net reclassification index (NRI). Furthermore, the confounding effects on the association among the mean standard uptake value of subcutaneous adipose tissue (SUVmean_SAT), American Joint Committee on Cancer (AJCC) stage, and progression status in patients with breast cancer were assessed.

Twenty-five out of 74 patients experienced recurrence during a median follow-up of 18 months. AJCC stage (p < 0.001) and SUVmean_SAT (p = 0.001) were significant independent prognostic factors. The AUC value and NRI of the combined Cox model (SUVmean_SAT plus AJCC stage) were higher than those of the Cox model based on AJCC stage alone. In addition, changes in the effect estimates showed a 12.2% decrease in hazard ratios when SUVmean_SAT was added to the AJCC stage model. High SUVmean_SAT was significantly associated with an increased risk of progression-free survival in patients with breast cancer.

A comprehensive assessment incorporating both SUVmean_SAT and AJCC stage may enhance understanding of the impact of adiposity on breast cancer prognosis.

## Linked entities

- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** SMN1 (survival of motor neuron 1, telomeric) [NCBI Gene 6606] {aka BCD541, GEMIN1, SMA, SMA1, SMA2, SMA3}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, CCNB1 (cyclin B1) [NCBI Gene 891] {aka CCNB}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, MKI67 (marker of proliferation Ki-67) [NCBI Gene 4288] {aka KIA, MIB-, MIB-1, PPP1R105}, HK1 (hexokinase 1) [NCBI Gene 3098] {aka CNSHA5, HK, HK1-ta, HK1-tb, HK1-tc, HKD}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, SAT1 (spermidine/spermine N1-acetyltransferase 1) [NCBI Gene 6303] {aka DC21, KFSD, KFSDX, SAT, SSAT, SSAT-1}
- **Diseases:** Obesity (MESH:D009765), gastric cancer (MESH:D013274), Cancer (MESH:D009369), metabolic syndrome (MESH:D024821), adipose inflammation (MESH:D007249), liver cancer (MESH:D006528), adipose (MESH:D018205), breast cancer (MESH:D001943), lymph node metastases (MESH:D008207), infection (MESH:D007239), colorectal cancer (MESH:D015179), metastases (MESH:D009362)
- **Chemicals:** Glucose (MESH:D005947), 18F-FDG (MESH:D019788), FDG-6-phosphate (-)
- **Species:** Meleagris gallopavo (common turkey, species) [taxon 9103], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12967984/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12967984/full.md

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Source: https://tomesphere.com/paper/PMC12967984