Associations between expression levels of nucleotide excision repair proteins in lymphoblastoid cells and risk of squamous cell carcinoma of the head and neck

被引:7
|
作者
Han, Peng [1 ,2 ,3 ]
Liu, Hongliang [1 ,2 ]
Shi, Qiong [1 ,2 ,4 ]
Liu, Zhensheng [1 ,2 ]
Troy, Jesse D. [1 ,5 ]
Lee, Walter T. [1 ,6 ]
Zevallos, Jose P. [7 ,8 ]
Li, Guojun [9 ,10 ,11 ]
Sturgis, Erich M. [9 ,10 ,11 ]
Wei, Qingyi [1 ,2 ,12 ]
机构
[1] Duke Univ, Med Ctr, Duke Canc Inst, 905 S LaSalle St, Durham, NC 27710 USA
[2] Duke Univ, Sch Med, Dept Med, Durham, NC 27706 USA
[3] Xi An Jiao Tong Univ, Affiliated Hosp 1, Coll Med, Dept Otorhinolaryngol Head & Neck Surg, Xian, Shaanxi, Peoples R China
[4] Fourth Mil Med Univ, Xijing Hosp, Dept Dermatol, Xian, Shaanxi, Peoples R China
[5] Duke Univ, Med Ctr, Div Blood & Marrow Transplantat, Durham, NC USA
[6] Duke Univ, Med Ctr, Dept Surg, Div Head & Neck Surg & Commun Sci, Durham, NC 27710 USA
[7] Washington Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, St Louis, MO 63110 USA
[8] Univ N Carolina, Dept Epidemiol, Gillings Sch Global Publ Hlth, Chapel Hill, NC USA
[9] Univ Texas MD Anderson Canc Ctr, Dept Head, Houston, TX 77030 USA
[10] Univ Texas MD Anderson Canc Ctr, Dept Neck Surg, Houston, TX 77030 USA
[11] Univ Texas MD Anderson Canc Ctr, Dept Epidemiol, Houston, TX 77030 USA
[12] Duke Univ, Sch Med, Dept Populat Hlth Sci, Durham, NC USA
基金
美国国家卫生研究院;
关键词
biomarker; DNA repair; head and neck cancer; NER pathway; protein expression; MESSENGER-RNA EXPRESSION; INDUCED DNA-ADDUCTS; XERODERMA-PIGMENTOSUM; INTERNATIONAL HEAD; CANCER STATISTICS; POOLED ANALYSIS; LUNG-CANCER; IN-VITRO; GENES; SUSCEPTIBILITY;
D O I
10.1002/mc.22801
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Squamous cell carcinoma of head and neck (SCCHN) is one of the most common malignancies worldwide, and nucleotide excision repair (NER) is involved in SCCHN susceptibility. In this analysis of 349 newly diagnosed SCCHN patients and 295 cancer-free controls, we investigated whether expression levels of eight core NER proteins were associated with risk of SCCHN. We quantified NER protein expression levels in cultured peripheral lymphocytes using a reverse-phase protein microarray. Compared with the controls, SCCHN patients had statistically significantly lower expression levels of ERCC3 and XPA (P = 0.001 and 0.001, respectively). After dividing the subjects by controls' median values of expression levels, we found a dose-dependent association between an increased risk of SCCHN and low expression levels of ERCC3 (adjusted OR, 1.75, and 95% CI: 1.26-2.42; P-trend = 0.008) and XPA (adjusted OR, 1.88; 95% CI, 1.35-2.60; P-trend = 0.001). We also identified a significant multiplicative interaction between smoking status and ERCC3 expression levels (P = 0.014). Finally, after integrating demographic and clinical variables, we found that the addition of ERCC3 and XPA expression levels to the model significantly improved the sensitivity of the expanded model on SCCHN risk. In conclusion, reduced protein expression levels of ERCC3 and XPA were associated with an increased risk of SCCHN. However, these results need to be confirmed in additional large studies.
引用
收藏
页码:784 / 793
页数:10
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