# Proteomic Profiling Reveals TPR and FGA as Predictive Serum Biomarkers of Relapse to First- and Second-Generation EGFR-TKIs in Advanced Lung Adenocarcinoma

**Authors:** Pritsana Raungrut, Wararat Chiangjong, Thipphanet Masjon, Saowanee Maungchanburi, Thidarat Ruklert, Narongwit Nakwan

PMC · DOI: 10.3390/biomedicines13071608 · Biomedicines · 2025-06-30

## TL;DR

This study identifies TPR and FGA as potential blood markers to predict relapse after EGFR-TKI treatment in lung cancer patients.

## Contribution

The study introduces TPR and FGA as novel serum biomarkers for predicting relapse after EGFR-TKI therapy in lung adenocarcinoma.

## Key findings

- TPR and FGA levels were significantly higher in patients with late relapse compared to early relapse.
- TPR and FGA showed strong diagnostic performance with AUCs of 0.946 and 0.809, respectively.
- The findings suggest TPR and FGA could help predict relapse after EGFR-TKI treatment.

## Abstract

Background: Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) significantly enhance the median survival of patients with lung adenocarcinoma (ADC) that harbor EGFR-sensitive mutations. However, most patients inevitably experience tumor relapse owing to drug resistance. We aimed to identify potential serum biomarkers for predicting post-EGFR-TKI treatment relapse in patients with advanced-stage lung ADC. Methods: Among 27 patients, including 6 and 21 with early and late relapse, respectively, differentially expressed proteins between patients with early and late relapses were identified using liquid chromatography and tandem mass spectrometry and subsequently validated using Western blotting. Predictive ability was assessed using the receiver operating characteristic curve and area under the curve (AUC) analysis. The association between the clinical variables and treatment response was evaluated using the chi-square test. Results: The serum expression levels of the translocated promoter region (TPR), junction plakoglobin (JUP), and fibrinogen alpha chain (FGA) were significantly higher in patients with late rather than early relapse. The findings indicated that TPR and FGA exhibited good diagnostic performance, with AUCs of 0.946 (p = 0.002; 95% confidence interval [CI], 0.84–1.05) and 0.809 (p = 0.034; 95% CI, 0.65–0.97), respectively. Conclusions: Our results suggest that the TPR and FGA levels are potential predictors of post-EGFR-TKI treatment relapse.

## Linked entities

- **Genes:** TPR (translocated promoter region, nuclear basket protein) [NCBI Gene 7175], FGA (fibrinogen alpha chain) [NCBI Gene 2243], JUP (junction plakoglobin) [NCBI Gene 3728]
- **Diseases:** lung adenocarcinoma (MONDO:0005061)

## Full-text entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, FGA (fibrinogen alpha chain) [NCBI Gene 2243] {aka AMYLD2, Fib2}, JUP (junction plakoglobin) [NCBI Gene 3728] {aka CTNNG, DP3, DPIII, PDGB, PG, PKGB}
- **Diseases:** tumor (MESH:D009369), ADC (MESH:D000230), Lung Adenocarcinoma (MESH:D000077192)
- **Species:** 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/PMC12292068/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12292068/full.md

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Source: https://tomesphere.com/paper/PMC12292068