| Literature DB >> 28356981 |
Trang T B Pham1, Naohide Oue1, Manabu Yamamoto2, Megumu Fujihara3, Teruyoshi Ishida4, Shoichiro Mukai1, Naoya Sakamoto1, Kazuhiro Sentani1, Wataru Yasui1.
Abstract
Approximately 70 years have passed since the atomic bombs were dropped on Nagasaki and Hiroshima. To elucidate potential biomarkers and possible mechanisms of radiation-induced cancer, the expression of FKTN, which encodes fukutin protein and causes Fukuyama-type congenital muscular dystrophy, was analyzed in gastric cancer (GC) tissue samples from atomic bomb survivors. Expression of cluster of differentiation (CD) 10 was also evaluated, as it has previously been observed that positive fukutin expression was frequently noted in CD10-positive GC cases. In the first cohort from Hiroshima Red Cross Hospital and Atomic-Bomb Survivors Hospital (Hiroshima, Japan; n=92), 102 (53%) of the GC cases were positive for fukutin. Expression of fukutin was not associated with exposure status, but was associated with CD10 expression (P=0.0001). The second cohort was from Hiroshima University Hospital (Hiroshima, Japan; n=86), and these patients were also in the Life Span Study cohort, in which atomic bomb radiation doses were precisely estimated using the DS02 system. Expression of fukutin was detected in 58 (67%) of GC cases. GC cases positive for fukutin were observed more frequently in the low dose-exposed group than in the high dose-exposed group (P=0.0001). Further studies with a larger cohort, including precise radiation dose estimation, may aid in clarifying whether fukutin could serve as a potential biomarker to define radiation-induced GC in atomic-bomb survivors.Entities:
Keywords: FKTN; atomic bomb; fukutin; gastric cancer; radiation carcinogenesis
Year: 2016 PMID: 28356981 PMCID: PMC5351402 DOI: 10.3892/ol.2016.5520
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967