Abstract

BackgroundDiagnosis of esophageal squamous cell carcinoma (SCC) may improve with early diagnosis. Currently it is difficult to diagnose SCC in the early stage because there is a limited number of tumor markers available.ResultsFifty-two esophageal SCC SEREX antigens were identified by SEREX (serological identification of antigens by recombinant cDNA expression cloning) using a cDNA phage library and sera of patients with esophageal SCC. Sequence analysis revealed that three of these antigens were similar in amino acid sequences, and they were designated as ECSA (esophageal carcinoma SEREX antigen)-1, -2 and -3. The ECSA family was also similar to an EST clone, hepatocellular carcinoma-associated antigen 25a (HCA25a). Serum antibody levels to ECSA-1, -2 and -3 were significantly higher in patients with esophageal SCC than in healthy donors. Based on the conserved amino acid sequences, three peptides were synthesized and used for enzyme-linked immunosorbent assays (ELISA). The serum antibody levels against one of these peptides were significantly higher in patients with esophageal SCC. This peptide sequence was also conserved in FAM119A, GOSR1 and BBS5, suggesting that these are also ECSA family members. Reverse transcription followed by quantitative PCR analysis showed that the mRNA expression levels of ECSA-1, -2 and -3 and FAM119A but not of HCA25a, GOSR1 and BBS5 were frequently elevated in esophageal SCC tissues.ConclusionsWe have identified a new gene family designated ECSA. Serum antibodies against the conserved domain of the ECSA family may be a promising tumor marker for esophageal SCC.

Highlights

  • Diagnosis of esophageal squamous cell carcinoma (SCC) may improve with early diagnosis

  • Serological screening of cDNA Library A phage expression library was constructed from the mRNA of an esophageal SCC cell line, T.Tn

  • Expression of ECSA in esophageal SCC The expression of the ECSA family members was examined by realtime RT-PCR, and the results showed that the mRNA expression levels of ECSA-1, -2 and -3 and FAM119A were elevated more frequently in tumor tissues than in the surrounding normal tissues (Figure 7a, b, c and 7e; Additional File 3)

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Summary

Introduction

Diagnosis of esophageal squamous cell carcinoma (SCC) may improve with early diagnosis. Despite improvements in surgical techniques and adjuvant chemoradiotherapy, many patients suffer from rapid recurrence of the disease and have a poor prognosis [4]. Several tumor markers have been identified in esophageal SCC, they are not sufficiently prevalent to allow for use as a general diagnostic tool [5,6,7]. It has been known for several decades that the immune system is able to recognize tumor cells [8,9], and by

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