Characteristics of Gastric Carcinomas With High ERCC1 Expression and the Prognostic Value of ERCC1 Expression.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 18 04 2020
revised: 28 04 2020
accepted: 29 04 2020
entrez: 4 6 2020
pubmed: 4 6 2020
medline: 13 6 2020
Statut: ppublish

Résumé

We aimed to evaluate the characteristics of gastric carcinoma with high excision repair cross complementing 1 (ERCC1) expression and the prognostic value of ERCC1 expression. ERCC1 expression was evaluated by immunohistochemistry in 309 surgically resected gastric carcinoma specimens using a tissue microarray. Cancer-related survival was analysed using competing risk analysis. Compared to ERCC1-low gastric carcinomas, ERCC1-high gastric carcinomas showed less local invasion (p=0.0013), lower N stage (p=0.0302), earlier pTNM stage (p=0.0003), and less frequent recurrence (p=0002). Patients with ERCC1-high gastric carcinoma showed lower cumulative incidence function estimate of cancer-related death [3.37; 95% confidence intervaI (CI)=0.89-8.75] than did those with ERCC1-low gastric carcinoma (17.12; 95% CI=12.24-22.69; p-value by Gray's test=0.0012). Adjusted proportional sub-distribution hazard ratio for cancer-related death in the patients with ERCC1-high tumour was 0.272 (95% CI=0.084-0.878; p=0.0295). High ERCC1 expression may be an independent positive prognostic marker for gastric carcinoma.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
We aimed to evaluate the characteristics of gastric carcinoma with high excision repair cross complementing 1 (ERCC1) expression and the prognostic value of ERCC1 expression.
MATERIALS AND METHODS METHODS
ERCC1 expression was evaluated by immunohistochemistry in 309 surgically resected gastric carcinoma specimens using a tissue microarray. Cancer-related survival was analysed using competing risk analysis.
RESULTS RESULTS
Compared to ERCC1-low gastric carcinomas, ERCC1-high gastric carcinomas showed less local invasion (p=0.0013), lower N stage (p=0.0302), earlier pTNM stage (p=0.0003), and less frequent recurrence (p=0002). Patients with ERCC1-high gastric carcinoma showed lower cumulative incidence function estimate of cancer-related death [3.37; 95% confidence intervaI (CI)=0.89-8.75] than did those with ERCC1-low gastric carcinoma (17.12; 95% CI=12.24-22.69; p-value by Gray's test=0.0012). Adjusted proportional sub-distribution hazard ratio for cancer-related death in the patients with ERCC1-high tumour was 0.272 (95% CI=0.084-0.878; p=0.0295).
CONCLUSION CONCLUSIONS
High ERCC1 expression may be an independent positive prognostic marker for gastric carcinoma.

Identifiants

pubmed: 32487614
pii: 40/6/3203
doi: 10.21873/anticanres.14301
doi:

Substances chimiques

Biomarkers, Tumor 0
DNA-Binding Proteins 0
ERCC1 protein, human EC 3.1.-
Endonucleases EC 3.1.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3203-3208

Informations de copyright

Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Jung Wook Yang (JW)

Department of Pathology, Gyeongsang National University School of Medicine, Jinju, Republic of Korea.
Department of Pathology, Gyeongsang National University Hospital, Jinju, Korea.

Jeong-Hee Lee (JH)

Department of Pathology, Gyeongsang National University School of Medicine, Jinju, Republic of Korea.
Department of Pathology, Gyeongsang National University Hospital, Jinju, Korea.
Gyungsang Institute of Health Science, Jinju, Republic of Korea.

Jong Sil Lee (JS)

Department of Pathology, Gyeongsang National University School of Medicine, Jinju, Republic of Korea.
Department of Pathology, Gyeongsang National University Hospital, Jinju, Korea.
Gyungsang Institute of Health Science, Jinju, Republic of Korea.

Dong Chul Kim (DC)

Department of Pathology, Gyeongsang National University School of Medicine, Jinju, Republic of Korea.
Department of Pathology, Gyeongsang National University Hospital, Jinju, Korea.
Gyungsang Institute of Health Science, Jinju, Republic of Korea.

Dae Hyun Song (DH)

Department of Pathology, Gyeongsang National University School of Medicine, Jinju, Republic of Korea.
Gyungsang Institute of Health Science, Jinju, Republic of Korea.
Department of Pathology, Changwon Gyeongsang National University Hospital, Changwon, Republic of Korea.

Se Min Jang (SM)

Department of Pathology, Changwon Gyeongsang National University Hospital, Changwon, Republic of Korea.

Hyo Jung An (HJ)

Department of Pathology, Changwon Gyeongsang National University Hospital, Changwon, Republic of Korea.

Hyun Min Koh (HM)

Department of Pathology, Changwon Gyeongsang National University Hospital, Changwon, Republic of Korea.

Minhye Kim (M)

Department of Pathology, Gyeongsang National University Hospital, Jinju, Korea.

Ji Min Na (JM)

Department of Pathology, Gyeongsang National University Hospital, Jinju, Korea.

Sang-Ho Jeong (SH)

Department of Surgery, Gyeongsang National University School of Medicine, Jinju, Republic of Korea.

Young-Joon Lee (YJ)

Department of Surgery, Gyeongsang National University School of Medicine, Jinju, Republic of Korea.

Gyung Hyuck Ko (GH)

Department of Pathology, Gyeongsang National University School of Medicine, Jinju, Republic of Korea gyunghko@gnu.ac.kr.
Department of Pathology, Gyeongsang National University Hospital, Jinju, Korea.
Gyungsang Institute of Health Science, Jinju, Republic of Korea.

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Classifications MeSH