Investigation of EGFR copy-number variations in skin cancers

被引:0
|
作者
Zhang, Jie [1 ,2 ,3 ]
Zhang, Richu [4 ]
Shao, Yong [1 ,2 ,3 ]
Chen, Bancheng [1 ,2 ,3 ]
Hu, Xiaoping [1 ,2 ,3 ]
Wan, Jun [1 ,3 ,5 ]
Zhang, Chao [1 ,3 ]
Zhang, Wei [1 ,5 ,6 ]
Yu, Bo [1 ,2 ,3 ]
机构
[1] Shenzhen PKU HKUST Med Ctr, Shenzhen Key Lab Translat Med Dermatol, Shenzhen 510632, Guangdong, Peoples R China
[2] Peking Univ, Shenzhen Hosp, Dept Dermatol, Shenzhen, Guangdong, Peoples R China
[3] Shenzhen PKU HKUST Med Ctr, Biomed Res Inst, Shenzhen 510632, Guangdong, Peoples R China
[4] Taizhou Municipal Hosp, Dept Gen Surg, Taizhou, Zhejiang, Peoples R China
[5] Hong Kong Univ Sci & Technol, Div Life Sci, Hong Kong, Hong Kong, Peoples R China
[6] Jinan Univ, JNU HKUST Joint Lab, Guangzhou, Guangdong, Peoples R China
来源
EUROPEAN JOURNAL OF ONCOLOGY | 2011年 / 16卷 / 01期
关键词
EGFR; copy-number variations (CNVs); basal cell carcinoma (BCC); squamous cell carcinoma (SCC); actinic keratosis (AK); GROWTH-FACTOR RECEPTOR; SQUAMOUS-CELL CARCINOMAS; GEFITINIB SENSITIVITY; GENE AMPLIFICATION; PROTEIN EXPRESSION; LUNG-CANCER; PHASE-II; HEAD; VALIDATION; RECURRENT;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim. The epidermal growth factor receptor (EGFR) family members play a considerable role in carcinogenesis. Copy number variations (CNVs) have been discovered to have phenotypic consequences and to be associated with various types of cancer. CNVs of EGFR were associated with cancer pathogenesis in recent studies. However, few studies were performed in skin cancer. In this study, we aim to examine the CNVs of EGFR in skin samples. Materials and methods. A total of 195 paired-samples including basal cell carcinoma (BCC), squamous cell carcinoma (SCC) and actinic keratosis (AK) were included. Real-time PCR was used for the quantification of EGFR copy numbers. Results. CNVs of EGFR showed statistical differences between cancer samples (both SCC and BCC) and normal tissues (p<0.05). Association analysis showed that the frequencies of EGFR's CNVs were correlated with the severity of skin abnormalities (p=0.011). Conclusions. CNVs of EGFR are associated with SCC and BCC but not with AK. Eur. J. Oncol., 16 (1), 15-19, 2011
引用
收藏
页码:15 / 19
页数:5
相关论文
共 50 条
  • [1] Examination of Smad2 and Smad4 copy-number variations in skin cancers
    Yong Shao
    Jie Zhang
    Richu Zhang
    Jun Wan
    Wei Zhang
    Bo Yu
    Clinical and Translational Oncology, 2012, 14 : 138 - 142
  • [2] Examination of Smad2 and Smad4 copy-number variations in skin cancers
    Shao, Yong
    Zhang, Jie
    Zhang, Richu
    Wan, Jun
    Zhang, Wei
    Yu, Bo
    CLINICAL & TRANSLATIONAL ONCOLOGY, 2012, 14 (02): : 138 - 142
  • [3] Copy-number variations and human disease
    Hegele, Robert A.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 81 (02) : 414 - 415
  • [4] Copy-number variations and human disease - Reply
    Wong, Kendy K.
    DeLeeuw, Ronald J.
    Brown, Carolyn J.
    Lam, Wan L.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 81 (02) : 415 - 415
  • [5] Copy-number variations associated with neuropsychiatric conditions
    Cook, Edwin H., Jr.
    Scherer, Stephen W.
    NATURE, 2008, 455 (7215) : 919 - 923
  • [6] Copy-number variations associated with neuropsychiatric conditions
    Edwin H. Cook Jr
    Stephen W. Scherer
    Nature, 2008, 455 : 919 - 923
  • [7] Copy-number variations associated with autism spectrum disorder
    Kakinuma, Hiroaki
    Sato, Hitoshi
    PHARMACOGENOMICS, 2008, 9 (08) : 1143 - 1154
  • [8] Copy-Number Variations, Noncoding Sequences, and Human Phenotypes
    Klopocki, Eva
    Mundlos, Stefan
    ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 12, 2011, 12 : 53 - 72
  • [9] Estimates of penetrance for recurrent pathogenic copy-number variations
    Rosenfeld, Jill A.
    Coe, Bradley P.
    Eichler, Evan E.
    Cuckle, Howard DPhil
    Shaffer, Lisa G.
    GENETICS IN MEDICINE, 2013, 15 (06) : 478 - 481
  • [10] MET Copy-Number Status in Lung Adenocarcinomas with EGFR Alterations
    Barletta, J. A.
    Xiao, Y.
    Joshi, V. A.
    Jackman, D. M.
    Janne, P. A.
    Lee, C.
    Lindeman, N. I.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2009, 11 (06): : 664 - 664