The Significance of Molecular Biomarkers on Clinical Survival Outcome Differs Depending on Colon Cancer Sidedness.


Journal

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

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 01 12 2019
revised: 10 12 2019
accepted: 12 12 2019
entrez: 2 1 2020
pubmed: 2 1 2020
medline: 11 1 2020
Statut: ppublish

Résumé

This retrospective study focused on the correlation between molecular markers and prognostic outcomes of colon cancer patients depending on sidedness. A total of 117 stage I-III colon cancer patients who underwent colectomy were enrolled. Novel methylation markers (KIF1A, PAX5 and VGF) were selected for epigenetic evaluation and p53 and ERCC1 protein expression was examined for the investigation of genetic alterations. High frequency of methylation was observed in 68.2% of right-sided and 39.7% of left-sided colon cancer cases (p=0.004). Abnormal p53 was identified in 52.3% of right-sided and 75.3% of left-sided cases (p=0.015). In right-sided cases, highly methylated genes demonstrated significantly favorable disease-free survival (p=0.049). Regarding left-sided cases, advanced T stage (p=0.028) and abnormal p53 (p=0.028) were revealed to be significant predictive factors of the disease-free survival outcome. Molecular alterations, as significant prognostic factors, might differ depending on the sidedness of colon cancers.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
This retrospective study focused on the correlation between molecular markers and prognostic outcomes of colon cancer patients depending on sidedness.
MATERIALS AND METHODS METHODS
A total of 117 stage I-III colon cancer patients who underwent colectomy were enrolled. Novel methylation markers (KIF1A, PAX5 and VGF) were selected for epigenetic evaluation and p53 and ERCC1 protein expression was examined for the investigation of genetic alterations.
RESULTS RESULTS
High frequency of methylation was observed in 68.2% of right-sided and 39.7% of left-sided colon cancer cases (p=0.004). Abnormal p53 was identified in 52.3% of right-sided and 75.3% of left-sided cases (p=0.015). In right-sided cases, highly methylated genes demonstrated significantly favorable disease-free survival (p=0.049). Regarding left-sided cases, advanced T stage (p=0.028) and abnormal p53 (p=0.028) were revealed to be significant predictive factors of the disease-free survival outcome.
CONCLUSION CONCLUSIONS
Molecular alterations, as significant prognostic factors, might differ depending on the sidedness of colon cancers.

Identifiants

pubmed: 31892568
pii: 40/1/201
doi: 10.21873/anticanres.13941
doi:

Substances chimiques

Biomarkers, Tumor 0
Neoplasm Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

201-211

Informations de copyright

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

Auteurs

Sho Hirabayashi (S)

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Masamichi Hayashi (M)

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan m-hayashi@med.nagoya-u.ac.jp.

Goro Nakayama (G)

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Shinji Mii (S)

Department of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Norifumi Hattori (N)

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Hiroshi Tanabe (H)

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Mitsuro Kanda (M)

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Chie Tanaka (C)

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Daisuke Kobayashi (D)

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Suguru Yamada (S)

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Masahiko Koike (M)

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Michitaka Fujiwara (M)

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Masahide Takahashi (M)

Department of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Yasuhiro Kodera (Y)

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

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Classifications MeSH