Abstract

Background: Esophageal squamous cell carcinoma (ESCC) acts as a fatal malignant tumor among human beings and is marked by late-stage diagnosis, frequent recurrence, metastasis, and therapy resistance. Tumor abnormal protein (TAP) remarkably affects cancer development and progression of human cancers. TAP has been shown to be a biomarker for gastric and lung cancer progression. Nevertheless, the clinical value exhibited by TAP for ESCC has not been well-explained in the current literature.Methods: The present study included 183 ESCC cases who received surgical resection and 183 cases who had normal physical checkup from March 2013 to January 2015 at the People's Hospital of Chizhou, and used the TAP detection agent for evaluating the TAP relative level.Results: As found, ESCC patients presented an obviously higher TAP expression relative to cases who had normal physical checkup. Moreover, TAP expression was significantly downregulated after surgery. Furthermore, the TAP expression was correlated with gender, smoking, pathologic differentiation, and pN stage, but not with age, tumor location, surgical type, pT stage, and vascular invasion. High expression of TAP was significantly correlated with poorer overall survival (OS) rate in ESCC patients. TAP was an independent prognostic predictor in ESCC patients, based on the multivariate survival analysis.Conclusion: The study reveals how TAP upregulation promotes ESCC malignant progression, and concludes that TAP acts as the therapeutic target and potential biomarker specific to ESCC.

Highlights

  • Up to now, esophageal cancer ranks seventh among all common cancer types and ranks sixth among all the causes that lead to cancer-related deaths all over the world

  • tumor abnormal protein (TAP) expression was significantly downregulated after surgery

  • The TAP expression was correlated with gender, smoking, pathologic differentiation, and pN stage, but not with age, tumor location, surgical type, pT stage, and vascular invasion

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Summary

Introduction

Esophageal cancer ranks seventh among all common cancer types and ranks sixth among all the causes that lead to cancer-related deaths all over the world. USSR scholars Kostyantin, A. and Galakhin identified the tumor abnormal protein (TAP), and many literatures revealed that TAP was closely associated with the progression and occurrence of numerous cancers [3, 4]. TAP results from the glycosylation changes regarding cancer cells. Like breast, ovarian, colon, endometrial, stomach, lung cancers, etc., the upregulation of TAP is seen [6]. TAP remarkably affects tumor development, progression, and metastasis, making it a significant indicator of tumor prognosis. Esophageal squamous cell carcinoma (ESCC) acts as a fatal malignant tumor among human beings and is marked by late-stage diagnosis, frequent recurrence, metastasis, and therapy resistance. Tumor abnormal protein (TAP) remarkably affects cancer development and progression of human cancers. The clinical value exhibited by TAP for ESCC has not been well-explained in the current literature

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