Journal of Experimental & Clinical Cancer Research (Apr 2020)

Urinary expression of let-7c cluster as non-invasive tool to assess the risk of disease progression in patients with high grade non-muscle invasive bladder Cancer: a pilot study

  • Manuela Spagnuolo,
  • Manuela Costantini,
  • Mariaconsiglia Ferriero,
  • Marco Varmi,
  • Isabella Sperduti,
  • Giulia Regazzo,
  • Lucia Cicchillitti,
  • Ana Belén Díaz Méndez,
  • Giovanni Cigliana,
  • Vincenzo Pompeo,
  • Andrea Russo,
  • Valentina Laquintana,
  • Riccardo Mastroianni,
  • Giulia Piaggio,
  • Umberto Anceschi,
  • Aldo Brassetti,
  • Alfredo Bove,
  • Gabriele Tuderti,
  • Rocco Simone Flammia,
  • Michele Gallucci,
  • Giuseppe Simone,
  • Maria Giulia Rizzo

DOI
https://doi.org/10.1186/s13046-020-01550-w
Journal volume & issue
Vol. 39, no. 1
pp. 1 – 11

Abstract

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Abstract Background High grade non-muscle-invasive bladder cancer (HG-NMIBC) is a heterogeneous disease with variable risk of progression. Urinary microRNAs are promising biomarkers for BC detection and surveillance. Let-7c-5p miRNA, clustered with miR-99a-5p and -125b-5p, is deregulated in cancer, including BC. The aim of this study is to evaluate urinary let-7c cluster expression in Ta/T1 HG-NMIBC patients and its impact on progression-free survival (PFS). Methods Quantitative Real-Time-Polymerase-Chain-Reaction (qRT-PCR) was used to analyze the let-7c cluster expression in 57 urine and 49 neoplastic paired tissue samples prospectively collected from transurethral resection (TUR) HG-NMIBC patients. Twenty urine and 10 bladder tissue samples were collected and analyzed as normal controls. QRT-PCR was also used to detect intra−/extra-cellular let-7c cluster in BC cells. Receiver Operating Characteristic (ROC) curves were used to identify urinary miRNAs cut-off values predicting T-stage and PFS. Uni/multivariable Cox regression was performed to identify predictors of PFS. A nomogram predicting progression risk and a decision curve analysis (DCA) were performed. Results Urinary let-7c was significantly up-regulated in patients compared with controls, while the whole cluster was down-regulated in tumor tissues. Supporting these findings, in vitro comparison of extra−/intra-cellular ratios of cluster levels between BC cells, showed a higher ratio for let-7c in HG-NMIBC versus low-grade cells. Urinary let-7c cluster expression was increased in higher T-stage and was an independent predictor of progression. Lower EORTC-score and downregulation of urinary cluster were predictors of higher PFS on univariable Cox regression, while on multivariable analysis only cluster expression was an independent progression predictor. On DCA, a benefit was evident for patients with a PFS probability > 20%. Conclusions Urinary let-7c cluster evaluation may improve prognosis, identifying patients at risk of progression and addressing early radical treatment.

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