4.8 Article

FGFBP1 as a potential biomarker predicting bacillus Calmette-Guerin response in bladder cancer

Journal

FRONTIERS IN IMMUNOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.954836

Keywords

bladder cancer; bacillus Calmette-Guerin; FGFBP1; biomarker; PD-L1

Categories

Funding

  1. Natural Science Foundation Committee of China [NSFC 82073162]
  2. Natural Science Foundation of Guangdong Province of China [2021A1515010762]
  3. Outstanding Youth Development Scheme of Nanfang Hospital, Southern Medical University [2019J009]
  4. Dean's research fund of Nanfang Hospital, the Southern Medical University [2020Z005, 2019B008]
  5. Beijing Bethune Charitable Foundation [mnzl202017]

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Fibroblast growth factor binding protein 1 (FGFBP1) is upregulated in failures of BCG therapy and is associated with poor prognosis and immune escape in bladder cancer patients. There is a positive correlation between FGFBP1 and PD-L1 expression, making it a potential biomarker for accurately predicting BCG response.
Accurate prediction of Bacillus Calmette-Guerin (BCG) response is essential to identify bladder cancer (BCa) patients most likely to respond sustainably, but no molecular marker predicting BCG response is available in clinical routine. Therefore, we first identified that fibroblast growth factor binding protein 1 (FGFBP1) was upregulated in failures of BCG therapy, and the increased FGFBP1 had a poor outcome for BCa patients in the E-MTAB-4321 and GSE19423 datasets. These different expression genes associated with FGFBP1 expression are mainly involved in neutrophil activation, neutrophil-mediated immunity, and tumor necrosis factor-mediated signal pathways in biological processes. A significant positive correlation was observed between FGFBP1 expression and regulatory T-cell (Treg) infiltration by the Spearman correlation test in the BCG cohort (r = 0.177) and The Cancer Genome Atlas (TCGA) cohort (r = 0.176), suggesting that FGFBP1 may influence the response of BCa patients to BCG immunotherapy through immune escape. Though FGFBP1 expression was positively correlated with the expressions of PD-L1, CTLA4, and PDCD1 in TCGA cohort, a strong association between FGFBP1 and PD-L1 expression was only detected in the BCG cohort (r = 0.750). Furthermore, elevated FGFBP1 was observed in BCa cell lines and tissues in comparison to corresponding normal controls by RT-qPCR, Western blotting, and immunohistochemical staining. Increased FGFBP1 was further detected in the failures than in the responders by immunohistochemical staining. Notably, FGFBP1 is positively associated with PD-L1 expression in BCa patients with BCG treatment. To sum up, FGFBP1 in BCa tissue could be identified as a promising biomarker for the accurate prediction of BCG response in BCa.

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