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ADAR1 is a promising risk stratification biomarker of remnant liver recurrence after hepatic metastasectomy for colorectal cancer.

Authors :
Hata, Nanako
Shigeyasu, Kunitoshi
Umeda, Yuzo
Yano, Shuya
Takeda, Sho
Yoshida, Kazuhiro
Fuji, Tomokazu
Yoshida, Ryuichi
Yasui, Kazuya
Umeda, Hibiki
Takahashi, Toshiaki
Kondo, Yoshitaka
Kishimoto, Hiroyuki
Mori, Yoshiko
Teraishi, Fuminori
Yamamoto, Hideki
Michiue, Hiroyuki
Nakamura, Keiichiro
Tazawa, Hiroshi
Fujiwara, Toshiyoshi
Source :
Scientific Reports. 2/6/2023, Vol. 13 Issue 1, p1-10. 10p.
Publication Year :
2023

Abstract

Adenosine-to-inosine RNA editing is a process mediated by adenosine deaminases that act on the RNA (ADAR) gene family. It has been discovered recently as an epigenetic modification dysregulated in human cancers. However, the clinical significance of RNA editing in patients with liver metastasis from colorectal cancer (CRC) remains unclear. The current study aimed to systematically and comprehensively investigate the significance of adenosine deaminase acting on RNA 1 (ADAR1) expression status in 83 liver metastatic tissue samples collected from 36 patients with CRC. The ADAR1 expression level was significantly elevated in liver metastatic tissue samples obtained from patients with right-sided, synchronous, or RAS mutant-type CRC. ADAR1-high liver metastasis was significantly correlated with remnant liver recurrence after hepatic metastasectomy. A high ADAR1 expression was a predictive factor of remnant liver recurrence (area under the curve = 0.72). Results showed that the ADAR1 expression level could be a clinically relevant predictive indicator of remnant liver recurrence. Patients with liver metastases who have a high ADAR1 expression requires adjuvant chemotherapy after hepatic metastasectomy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20452322
Volume :
13
Issue :
1
Database :
Academic Search Index
Journal :
Scientific Reports
Publication Type :
Academic Journal
Accession number :
161748140
Full Text :
https://doi.org/10.1038/s41598-023-29397-z