Different Susceptibility of Each L‐myc Genotype to Esophageal Cancer Risk Factors
Author(s) -
Kumimoto Hiroshi,
Hamajima Nobuyuki,
Nishizawa Kimiko,
Nishimoto Yoshio,
Matsuo Keitaro,
Harada Hideki,
Shinoda Masayuki,
Hatooka Shunzo,
Ishizaki Kanji
Publication year - 2001
Publication title -
japanese journal of cancer research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.035
H-Index - 141
eISSN - 1349-7006
pISSN - 0910-5050
DOI - 10.1111/j.1349-7006.2001.tb01155.x
Subject(s) - genotype , odds ratio , esophageal cancer , medicine , gastroenterology , allele , polymorphism (computer science) , risk factor , cancer , biology , genetics , gene
To understand the relationship between the L‐myc genotypes and esophageal cancer risk, a polynierase chain reaction‐based restriction fragment length polymorphism analysis was performed on 91 Japanese patients with esophageal cancer and 241 non‐cancer outpatients. No significant difference in the distribution of genotypes was observed between patients and controls; 18.7% LL genotype, 56.0% LS and 25.3% SS among patients, and 24.5%, 55.6% and 19.9%, respectively, among controls. Frequency of the s‐allele in patients (0.533) was slightly higher than in controls (0.477), but the difference was not statistically significant. However, the odds ratios (ORs) for smoking or heavy drinking were markedly higher in SS and LS genotypes than in LL genotype; age‐sex‐adjusted ORs for smoking was 7.57 in the SS genotype, 6.40 in the LS genotype and 1.77 in the LL genotype. Age‐sex‐adjusted ORs for heavy drinking were 19.78, 18.20 and 7.40, respectively. The age‐sex‐adjusted ORs for both factors combined were 12.77, 18.45 and 1.44, respectively. These results suggested that the L‐myc polymorphism might modify the effects of lifestyle factors on esophageal cancer risk.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom