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  1. 医学部
  1. 医学部
  2. 学術雑誌掲載論文  (医学部)

XPC intron11 C/A polymorphism as a risk factor for prostate cancer

http://hdl.handle.net/10458/0002000473
http://hdl.handle.net/10458/0002000473
44dcd7af-5ffd-4973-9419-c6b3b71f2eca
Item type 学術雑誌論文 / Journal Article(1)
公開日 2024-01-31
タイトル
タイトル XPC intron11 C/A polymorphism as a risk factor for prostate cancer
言語 en
言語
言語 eng
キーワード
言語 en
主題Scheme Other
キーワード Cancer risk
キーワード
言語 en
主題Scheme Other
キーワード DNA repair gene
キーワード
言語 en
主題Scheme Other
キーワード Prostate cancer
キーワード
言語 en
主題Scheme Other
キーワード XPC-PAT
キーワード
言語 en
主題Scheme Other
キーワード Xeroderma pigmentosum
資源タイプ
資源タイプ journal article
アクセス権
著者 吉野, 喜裕

× 吉野, 喜裕

WEKO 27589

ja 吉野, 喜裕

ja-Kana ヨシノ, ヨシヒロ

en Yoshino, Yoshihiro


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竹内, 昌平

× 竹内, 昌平

WEKO 22917

ja 竹内, 昌平

ja-Kana タケウチ, ショウヘイ

en Takeuchi, Shouhei


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Katoh, Takahiko

× Katoh, Takahiko

WEKO 27596

en Katoh, Takahiko


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黒田, 嘉紀

× 黒田, 嘉紀

WEKO 22781
e-Rad 50234620

en Kuroda, Yoshiki

ja 黒田, 嘉紀

ja-Kana クロダ, ヨシキ


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抄録
内容記述タイプ Abstract
内容記述 Objectives: DNA repair genes play an important role in protection against environmental and endogenous DNA damage, and constitute the first line of defense against cancer. Xeroderma pigmentosum complementation group C (XPC) is involved in the damage recognition step during nucleotide excision repair. The relationship between XPC intron11 C/A polymorphism and cancer risk has not been widely studied. Hence, this study evaluated the relationship between the XPC intron11 C/A polymorphism and prostate cancer risk.

Materials and methods: This hospital-based cohort consisted of 152 patients with prostate cancer and 142 male controls. The XPC intron11 C/A genotype was determined using the PCR-RFLP method. Medical, occupational, and cigarette-smoking history was obtained from each participant using questionnaires.

Results: Logistic regression analysis revealed that compared to controls, the frequencies of the A/A and C/A genotypes were significantly higher than those of the C/C genotype in cancer patients (OR = 2.03, 95% confidence interval (CI) 1.03-3.98 and OR = 1.91, 95% CI 1.13-3.24, respectively). We also found that the frequency of the A/A genotype was significantly higher in cancer cases than in controls among non-smokers (OR = 7.7, 95% CI 1.38-42.88, compared to the C/C genotype).

Conclusion: We found that the XPC intron11 C/A polymorphism was associated with an increased risk of prostate cancer. Among non-smokers, the A/A genotype was significantly more prevalent in prostate cancer patients than in controls.
言語 en
内容記述
内容記述タイプ Other
内容記述 Citation:
Yoshino Y, Takeuchi S, Katoh T, Kuroda Y. XPC intron11 C/A polymorphism as a risk factor for prostate cancer. Environ Health Prev Med. 2016 Mar;21(2):100-4. doi: 10.1007/s12199-015-0505-z. Epub 2016 Jan 8. PMID: 26745975; PMCID: PMC4771637.
言語 en
書誌情報 en : Environmental Health and Preventive Medicine

巻 21, 号 2, p. 100-104, 発行日 2016-03
出版者
出版者 The Japanese Society for Hygiene
言語 en
ISSN
収録物識別子タイプ ISSN
収録物識別子 1342-078X
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1007/s12199-015-0505-z
著者版フラグ
出版タイプ NA
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Cite as

吉野, 喜裕, 竹内, 昌平, Katoh, Takahiko, 黒田, 嘉紀, 2016, XPC intron11 C/A polymorphism as a risk factor for prostate cancer: The Japanese Society for Hygiene, 100–104 p.

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