Abstract

Esophageal squamous carcinoma (ESCC) has a high morbidity and mortality rate. Identifying risk metabolites associated with its progression is essential for the early prevention and treatment of ESCC. A total of 373 ESCC, 40 esophageal squamous dysplasia (ESD), and 218 healthy controls (HC) subjects were enrolled in this study. Gas chromatography-mass spectrometry (GC/MS) was used to acquire plasma metabolic profiles. Receiver operating characteristic curve (ROC) and adjusted odds ratio (OR) were calculated to evaluate the potential diagnosis and prediction ability markers. The levels of alpha-tocopherol and cysteine were progressively decreased, while the levels of aminomalonic acid were progressively increased during the various stages (from precancerous lesions to advanced-stage) of exacerbation in ESCC patients. Alpha-tocopherol performed well for the differential diagnosis of HC and ESD/ESCC (AUROC>0.90). OR calculations showed that a high level of aminomalonic acid was not only a risk factor for further development of ESD to ESCC (OR>13.0) but also a risk factor for lymphatic metastasis in ESCC patients (OR>3.0). A low level of alpha-tocopherol was a distinguished independent risk factor of ESCC (OR< 0.5). The panel constructed by glycolic acid, oxalic acid, glyceric acid, malate and alpha-tocopherol performed well in distinguishing between ESD/ESCC from HC in the training and validation set (AUROC>0.95). In conclusion, the oxidative stress function was impaired in ESCC patients, and improving the body’s antioxidant function may help reduce the early occurrence of ESCC.

Highlights

  • Esophageal cancer (EC) is the seventh most common cancer and the sixth most common cause of cancer death globally, causing about 572 000 new cases and 509 000 deaths worldwide [1]

  • Samples for this study were collected at the First Affiliated Hospital of Nanjing Medical University, and the sampling period was from June 2019 to June 2021

  • A total of 631 subjects were included in this study, including 218 healthy controls (HC), 373 with esophageal squamous cell carcinoma (ESCC) and 40 with esophageal squamous dysplasia (ESD)

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Summary

Introduction

Esophageal cancer (EC) is the seventh most common cancer and the sixth most common cause of cancer death globally, causing about 572 000 new cases and 509 000 deaths worldwide [1]. Esophageal squamous cell carcinomas (ESCC) are the most common histological type of EC, accounting for approximately 90% of esophageal cancer cases worldwide [2]. ESCC, accounting for approximately 50% of all ESCC cases worldwide [3, 4]. Esophageal squamous dysplasia (ESD) is a primary precancerous lesion for ESCC, with a significantly increased risk of developing into ESCC [6]. Surveying the metabolic change and associated risk factors occurring during ESCC and establishing suitable non-invasive adjunctive assays development could provide implications for early diagnosis and potential therapeutic strategies

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