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The Prevalence of Cancer-Associated Autoantibodies in Patients with Gastric Cancer and Progressive Grades of Premalignant Lesions
被引:24
|作者:
Meistere, Irena
[1
]
Werner, Simone
[2
]
Zayakin, Pawel
[1
]
Silina, Karina
[1
]
Rulle, Undine
[1
]
Pismennaja, Angelina
[1
]
Santare, Daiga
[3
,4
,5
]
Kikuste, Ilze
[3
,4
,6
]
Isajevs, Sergejs
[3
,4
,5
]
Leja, Marcis
[3
,4
,5
,6
]
Kupcinskas, Limas
[7
,8
]
Kupcinskas, Juozas
[7
,8
]
Jonaitis, Laimas
[7
,8
]
Wu, Chun-Ying
[9
]
Brenner, Hermann
[2
,10
,11
,12
]
Line, Aija
[1
]
Kalnina, Zane
[1
]
机构:
[1] Latvian Biomed Res & Study Ctr, Canc Biomarker & Immunotherapy Grp, Riga, Latvia
[2] German Canc Res Ctr, Div Clin Epidemiol & Aging Res, Heidelberg, Germany
[3] Univ Latvia, Inst Clin & Prevent Med, Riga, Latvia
[4] Univ Latvia, Fac Med, Riga, Latvia
[5] Riga East Univ Hosp, Riga, Latvia
[6] Digest Dis Ctr GASTRO, Riga, Latvia
[7] Lithuanian Univ Hlth Sci, Med Acad, Inst Digest Res, Kaunas, Lithuania
[8] Lithuanian Univ Hlth Sci, Med Acad, Dept Gastroenterol, Kaunas, Lithuania
[9] Taichung Vet Gen Hosp, Div Gastroenterol & Hepatol, Taichung, Taiwan
[10] German Canc Res Ctr, Div Prevent Oncol, Heidelberg, Germany
[11] Natl Ctr Tumor Dis NCT, Heidelberg, Germany
[12] German Canc Res Ctr, German Canc Consortium DKTK, Heidelberg, Germany
关键词:
TUMOR-ASSOCIATED ANTIGENS;
LUNG-CANCER;
CANCER/TESTIS ANTIGENS;
NY-ESO-1;
EXPRESSION;
P53;
AUTOANTIBODIES;
ESOPHAGEAL CANCER;
SERUM PEPSINOGEN;
CELL CARCINOMA;
FOLLOW-UP;
ADENOCARCINOMAS;
D O I:
10.1158/1055-9965.EPI-17-0238
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background: Serum autoantibodies against tumor-associated antigens (TAAs) are detectable in early-stage gastric cancer patients; however, the time point during cancerogenesis when they appear in circulation is still obscure. Methods: In this study, we developed a recombinant antigen microarray and analyzed the prevalence of autoantibodies against 102 TAAs in 829 gastric cancer patients and 929 healthy controls from Caucasian and Asian populations, as well as 100 patients with chronic atrophic gastritis and 775 individuals staged according to different grades of intestinal metaplasia. Results: Six antigens, including CTAG1B/CTAG2, DDX53, IGF2BP2, TP53, and MAGEA3, were predominantly reacting with sera from gastric cancer patients when compared with healthy controls, and the seroreactivity was associated with intestinal-type gastric cancer, but not with patients' Helicobacter pylori status, grade, age, gender, or stage of gastric cancer. We detected gastric cancer-associated seroreactivity in 13% of patients with advanced/severe intestinal metaplasia, which was increased in comparison with mild/moderate intestinal metaplasia (5.3%) and was comparable with that seen in early-stage gastric cancer patients (12%). Moreover, by testing serum samples taken 1 to 9 years before the clinical diagnosis of 18 incident gastric cancer cases, we detected autoantibody responses against several TAAs-SOX2, MYC, BIRC5, IGF2BP1, and MUC1. Conclusions: Our results suggest that humoral immune response against TAAs is generated already during premalignant stages. Impact: Based on the obtained results, cancer-associated auto-antibodiesmight make a valuable contribution to the stratification of high-risk patients with premalignant lesions in the stomach through enhancing the positive predictive power of existing risk models. Cancer Epidemiol Biomarkers Prev; 26(10); 1564-74. (C) 2017 AACR.
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页码:1564 / 1574
页数:11
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