Detection of serum p53 antibodies in patients with esophageal squamous cell carcinoma: correlation with clinicopathologic features and tumor markers.

Author(s):  
H Shimada ◽  
K Nakajima ◽  
T Ochiai ◽  
Y Koide ◽  
S I Okazumi ◽  
...  
2018 ◽  
Vol 31 (Supplement_1) ◽  
pp. 135-135
Author(s):  
Hideaki Shimada ◽  
Satoshi Yajima ◽  
Yoko Oshima ◽  
Masaaki Ito ◽  
Tatsuki Nanami ◽  
...  

Abstract Background Serum antibodies are induced even ata the eraly phase of carcinogenesis. Serum p53 antibodies (s-p53-Abs) have been developed and approved as routine blood test for monitoring esophageal squamous cell carcinoma (SCC). Recently, we have developed new ELISA systems to detect serum anti-IgG auto-antibodies against tumor antigens in patients with esophageal (SCC). In this paper, we focused on serum auto-antibodies against p53, NY-ESO-1, Galectin-1 and RalA. Methods Serum samples of patients with esophageal SCC were obtained before surgery. Serum anti-IgG antibodies against several tumor antigens were analyzed by newly developed ELISA systems. Target tumor antigens were p53, NY-ESO-1, Galectin-1 and RalA. Cut-off values were fixed using mean + 3SD of values of a total of 74 healthy controls. Changing pattern of serum p53 antibodies titers was also assessed during postoperative follow-up. Results Positive rates of serum antibodies were 18% for p53, 31% for NY-ESO-1, 10% for Galectin-1 and 9% for RalA. Positive rates of these antibodies in healthy controls were 0%. Combination assay improved positive rates without increased false positive rates as follows; p53 + NY-ESO-1 = 40%, p53 + NY-ESO-1 + Galectin-1 = 47%, p53 + NY-ESO-1 + Galectin-1 + RalA = 51%. Although some patients with extremely-high antibody titer for p53 persistently positive even after curative surgery, changing patterns of serum titers seemed to be associated with clinical outcome. Conclusion Although antibody titer of s-p53-Abs seemed to be associated with tumor burden, the titer gradually decresed at the last several months of the terminal stage. Such independent changing pattern of serum autoantibodies may have adding information to conventinal serum markers. We have developed new ELISA system to detect serum autoantibodies for patients with esophageal SCC. Although the positive rates of single serum auto-antibody were still relatively low, combination assay with plural auto-antibodies may be useful. Disclosure All authors have declared no conflicts of interest.


Odontology ◽  
2008 ◽  
Vol 96 (1) ◽  
pp. 32-37 ◽  
Author(s):  
Yutaka Yamazaki ◽  
Itsuo Chiba ◽  
Makoto Ishikawa ◽  
Chiharu Satoh ◽  
Ken-ichi Notani ◽  
...  

2021 ◽  
Author(s):  
Zhangjiao Wang ◽  
Yong Shen ◽  
Qingxia Xu

Abstract Objective: To seek potential metastatic tumor markers in esophageal squamous cell carcinoma (ESCC) by bioinformatics. Methods: Four datasets (GSE70409, GSE26886, GSE161533, GSE17351) were downloaded from GEO database, and the differential expression of mRNA was screened by Limma software package. Gene ontology function and kyoto encyclopedia of genes and genomes pathway enrichment analysis were performed using the database for annotation; Protein–protein interaction network of these DEGs was constructed based on STRING database; then, the hub gene were identified by six algorithms of Cytoscape software. Using GEPIA2 database and OncoLnc database to analyze the survival of hub genes. Immune infiltration was analyzed by TIMER2 database and CIBERSORT deconvolution method. Results: A total of 244 differentially expressed genes(DEGs)were screened from 4 data sets of GEO database, including 164 up-regulated genes and 80 down-regulated genes, which were mainly enriched at extracellular region and extracellular space, and involved in biological processes such as cell adhesion and proteolysis related to tumor invasion and metastasis. KEGG results showed that DEGs were mainly enriched in PI3K-Akt signal pathway and extracellular matrix (ECM) receptor interaction signal pathway. Through the protein interaction analysis of DEGs, we found that three hub genes (CXCL8, MMP9 and MMP13) were highly expressed in ESCC. However, the GEPIA2 database shows that only CXCL8 is associated with the overall survival of ESCC patients. The results of immune infiltration showed that macrophages and resting dendritic cells increased significantly, while mast cells and monocytes decreased significantly. Conclusion: Three hub genes and immune infiltrating cells may play an important role in ESCC, and are expected to become potential tumor markers of ESCC and be used in the diagnosis and treatment of ESCC.


2019 ◽  
Vol 87 ◽  
pp. 1-10 ◽  
Author(s):  
Farhadul Islam ◽  
Vinod Gopalan ◽  
Simon Law ◽  
Johnny Cheuk-on Tang ◽  
Alfred King-yin Lam

Cancer ◽  
2000 ◽  
Vol 89 (8) ◽  
pp. 1677-1683 ◽  
Author(s):  
Hideaki Shimada ◽  
Akihiko Takeda ◽  
Miwako Arima ◽  
Shinichi Okazumi ◽  
Hisahiro Matsubara ◽  
...  

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