Abstract

This study proposed label-free fluorescence lifetime imaging and phasor analysis methods to discriminate different grades of cervical intraepithelial neoplasia (CIN). The human cervical tissue lesions associated with cellular metabolic abnormalities were detected by the status changes of important coenzymes in cells and tissues, reduced nicotinamide adenine dinucleotide (phosphate) (NAD(P)H) and flavin adenine dinucleotide (FAD). Fluorescence lifetime imaging microscopy (FLIM) was used to study human cervical tissues, human cervical epithelial cells, and standard samples. Phasor analysis was applied to reveal the interrelation between the metabolic changes and cancer development, which can distinguish among different stages of cervical lesions from low risk to high risk. This approach also possessed high sensitivity, especially for healthy sites of CIN3 tissues, and indicated the dominance of the glycolytic pathway over oxidative phosphorylation in high-grade cervical lesions. This highly adaptive, sensitive, and rapid diagnostic tool exhibits a great potential for cervical precancer diagnosis.

Highlights

  • Cervical cancer is one of the leading causes of cancer deaths in women, and it is the fourth most common malignant tumor in women worldwide, with about 530,000 new cases and 270,000 deaths each year [1,2,3]

  • Cervical cancer usually develops from cervical intraepithelial neoplasia (CIN), which is a precancerous lesion categorized as low-grade squamous intraepithelial lesions (LSIL) and high-grade squamous intraepithelial lesions (HSIL)

  • HSIL includes moderate dysplasia and severe dysplasia, which are of high risk and may develop into cervical cancer [4,5,6]

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Summary

Introduction

Cervical cancer is one of the leading causes of cancer deaths in women, and it is the fourth most common malignant tumor in women worldwide, with about 530,000 new cases and 270,000 deaths each year [1,2,3]. Cervical cancer usually develops from cervical intraepithelial neoplasia (CIN), which is a precancerous lesion categorized as low-grade squamous intraepithelial lesions (LSIL) and high-grade squamous intraepithelial lesions (HSIL). LSIL is sometimes called CIN1, which is of low risk and usually resolves without treatment. HSIL includes moderate dysplasia ( called CIN2) and severe dysplasia ( called CIN3), which are of high risk and may develop into cervical cancer [4,5,6]. The transformation from human papillomavirus (HPV) infection into cervical cancer takes about 5-10 years; but if cervical cancer is diagnosed at an early stage, or is found at the CIN stage of precancer, the chance of a cure can be greatly increased [7]. Early detection and diagnosis of precancerous lesions are essential for appropriate treatment

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