Possible predictive significance of serum RalA autoantibodies on relapse‑free survival in patients with colorectal cancer
Author(s) -
Mitsunori Ushigome,
Hideaki Shimada,
Yoshihiro Nabeya,
Fumiaki Shiratori,
Hiroaki Soda,
Nobuhiro Takiguchi,
Isamu Hoshino,
Akiko Kuwajima,
Tomoaki Kaneko,
Kimihiko Funahashi
Publication year - 2020
Publication title -
molecular and clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.442
H-Index - 7
eISSN - 2049-9469
pISSN - 2049-9450
DOI - 10.3892/mco.2020.2180
Subject(s) - carcinoembryonic antigen , colorectal cancer , cancer , medicine , oncogene , antibody , stage (stratigraphy) , antigen , gastroenterology , oncology , immunology , biology , cell cycle , paleontology
RalA protein, a member of the Ras superfamily of small GTPases, is a tumor antigen that induces serum RalA antibodies (s-RalA-Abs). The present study explored the clinicopathological and prognostic significance of s-RalA-Abs in patients with colorectal cancer. Serum samples were obtained from 314 patients with colorectal cancer at stage 0/I (n=71), stage II (n=86), stage III (n=78), stage IV (n=64) and recurrence (n=15). Samples were analyzed for the presence of s-RalA-Abs using ELISA. The cutoff optical density value was fixed at 0.324 (mean of heathy controls + 3 standard deviations). The overall positive rate for serum anti-RalA antibodies was 14%. The presence of s-RalA-Abs was not significantly associated with clinicopathological characteristic factors. Additionally, the s-RalA-Abs(+) group demonstrated significantly poor relapse-free survival rates. The s-RalA-Abs (+)/carcinoembryonic antigen (CEA)(+) group exhibited the worst prognosis and s-RalA-Abs(+)/CEA(+) was an independent risk factor for poor relapse-free survival. Although the positive rate was not high, s-RalA-Abs may be a useful predictor of poor relapse-free survival in patients with colorectal cancer.
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