# The LBX2‐AS1–miR‐491‐5p–PKM2 Positive Feedback Loop Promotes Radiation Resistance of Esophageal Cancer by Enhancing Glycolysis

**Authors:** Fuhui Zhang, Zhiwu Wang, Xuemin Yao, Qingyu Zhang

PMC · DOI: 10.1155/bmri/1876375 · BioMed Research International · 2025-11-13

## TL;DR

This study identifies a feedback loop involving LBX2-AS1, miR-491-5p, and PKM2 that increases resistance to radiation in esophageal cancer by boosting glycolysis and altering the cell cycle.

## Contribution

The study reveals a novel positive feedback loop involving LBX2-AS1, miR-491-5p, and PKM2 that promotes radioresistance in esophageal cancer.

## Key findings

- LBX2-AS1 upregulation increases PKM2, HIF-1α, and cyclin D1, enhancing glycolysis and radioresistance.
- Downregulating LBX2-AS1 or miR-491-5p reduces cell proliferation, glycolysis, and radiation resistance.
- High LBX2-AS1 levels in patient serum correlate with worse survival and increased metastasis.

## Abstract

Radioresistance is a significant factor affecting the therapeutic efficacy of radiotherapy. This study is aimed at investigating the molecular mechanism by which LBX2‐AS1 regulates pyruvate kinase M2 (PKM2) to influence radioresistance and its potential as a biomarker for radioresistance in esophageal cancer.

Radioresistant sub‐cell lines, KYSE150R, were established in KYSE150 cells, and PKM2, cyclin D1, HIF‐1α, and LBX2‐AS1 levels were elevated in KYSE150R. Upregulated and downregulated PKM2 sub‐cell lines were established. Upregulating PKM2 increased the PKM2 level in the nucleus and increased levels of HIF‐1α, cyclin D1, and LBX2‐AS1. The knockdown of PKM2 showed the opposite result. Downregulated LBX2‐AS1 sub‐cell lines were established. Downregulation of LBX2‐AS1 decreased cell proliferation, glycolysis, cell cycle progression, and radioresistance, along with a reduction in cyclin D1, HIF‐1α, and PKM2 levels. The dual‐luciferase reporter system was used to verify that LBX2‐AS1 directly binds to miR‐491‐5p, and miR‐491‐5p directly binds to the 3 ′UTR of PKM2 mRNA. Downregulation of miR‐491‐5p in sh‐LBX2‐AS1 cells could increase cell proliferation, cell cycle, glycolysis, and radiation resistance. The LBX2‐AS1 level in serum of patients with esophageal cancer was detected, and its clinical relevance was analyzed. Results showed that high LBX2‐AS1 levels correlated with worse disease control, increased lymphatic metastasis, and poorer overall and progression‐free survival.

LBX2‐AS1‐miR‐491‐5p‐PKM2 positive feedback loop enhances the radioresistance of esophageal cancer cells by altering the cell cycle and enhancing glycolysis. High level of LBX2‐AS1 in serum was correlated with worse DCR, lymphatic metastasis, worse overall survival, and progression‐free survival.

## Linked entities

- **Genes:** LBX2-AS1 (LBX2 antisense RNA 1) [NCBI Gene 151534], PKM (pyruvate kinase M1/2) [NCBI Gene 5315], ccnd1.S (cyclin D1 S homeolog) [NCBI Gene 379161], HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091]
- **Proteins:** PKM (pyruvate kinase M1/2), HIF1A (hypoxia inducible factor 1 subunit alpha), ccnd1.S (cyclin D1 S homeolog)
- **Diseases:** esophageal cancer (MONDO:0007576)

## Full-text entities

- **Genes:** CCND1 (cyclin D1) [NCBI Gene 595] {aka BCL1, D11S287E, PRAD1, U21B31}, DCR (Down syndrome chromosome region) [NCBI Gene 1637] {aka DSCR}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, PKM (pyruvate kinase M1/2) [NCBI Gene 5315] {aka CTHBP, HEL-S-30, OIP3, PK3, PKM2, TCB}, LBX2-AS1 (LBX2 antisense RNA 1) [NCBI Gene 151534]
- **Diseases:** lymphatic metastasis (MESH:D008207), Esophageal Cancer (MESH:D004938)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** KYSE150R — Homo sapiens (Human), Esophageal squamous cell carcinoma, Cancer cell line (CVCL_C3LZ), KYSE150 — Homo sapiens (Human), Esophageal squamous cell carcinoma, Cancer cell line (CVCL_1348)

## Full text

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## Figures

37 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12612690/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12612690/full.md

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Source: https://tomesphere.com/paper/PMC12612690