Abstract

Bladder urothelial carcinoma (BC) is a common, recurrent, life-threatening, and unpredictable disease which is difficult to diagnose. These features make it one of the costliest malignancies. Although many possible diagnostic methods are available, molecular heterogeneity and difficulties in cytological or histological examination induce an urgent need to improve diagnostic techniques. Herein, we applied Fourier transform infrared spectroscopy in imaging mode (FTIR) to investigate patients' cytology samples assigned to normal (N), low-grade (LG) and high-grade (HG) BC. With unsupervised hierarchical cluster analysis (UHCA) and hematoxylin-eosin (HE) staining, we observed a correlation between N cell types and morphology. High-glycogen superficial (umbrella) and low-glycogen piriform urothelial cells, both with normal morphology, were observed. Based on the spectra derived from UHCA, principal component analysis (PCA) and partial least squares discriminant analysis (PLS-DA) were performed, indicating a variation of protein content between the patient groups. Moreover, BC spectral cytology identified a low number of high-glycogen cells for which a shift of the carbohydrate/phosphate bands was also observed. Despite high cellular heterogeneity, PLS-DA was able to classify the spectra obtained. The voided urine FTIR cytology is one of the options that might be helpful in BC diagnosis, as high sensitivity and specificity up to 97% were determined.

Highlights

  • IntroductionBladder urothelial carcinoma (BC) cytological diagnosis awkwardness is broadly discussed in the literature [1,2]

  • Licensee MDPI, Basel, Switzerland.Bladder urothelial carcinoma (BC) cytological diagnosis awkwardness is broadly discussed in the literature [1,2]

  • According to standard hematoxylin and eosin (HE) cytological examination of voided urine, 45 patients were grouped into three groups with normal cytology (N), low-grade BC (LG BC) and highgrade BC (HG BC)

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Summary

Introduction

Bladder urothelial carcinoma (BC) cytological diagnosis awkwardness is broadly discussed in the literature [1,2]. This commonly used diagnostic method is based on examination of many subjective morphological features of cells present in urine, which, according to the diagnostic standard, are usually stained with hematoxylin and eosin (HE). Diagnosis is put forward after tissue excision and the occurrence of a thickened urothelium with disrupted stratification. In spite of this diagnostic pitfall, LG BC rarely infiltrates, and often creates papillary structures which are visible in cystoscopy and ultrasound [1,3,4,5]. BC cytology is cumbersome and subjective, but apart from this, it is cost-effective and satisfactory in the detection of highly malignant HG BC [6]

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