Genetic aberrations detected by comparative genomic hybridisation in vulvar cancers

被引:0
作者
D G Allen
A-M Hutchins
F Hammet
D J White
J P Scurry
S N Tabrizi
S M Garland
J E Armes
机构
[1] Mercy Hospital for Women,Department of Gynecologic Oncology
[2] Mercy Hospital for Women,Department of Pathology
[3] Molecular Pathology Laboratory,Department of Pathology
[4] Victorian Breast Cancer Research Consortium,Department of Microbiology and Infectious Diseases
[5] University of Melbourne and Peter MacCallum Cancer Institute,Department of Anatomical Pathology
[6] University of Melbourne and Peter MacCallum Cancer Institute,undefined
[7] Royal Women's Hospital,undefined
[8] Women's and Children's Health,undefined
[9] Royal Women's Hospital,undefined
[10] Women's and Children's Health,undefined
来源
British Journal of Cancer | 2002年 / 86卷
关键词
comparative genomic hybridisation; vulva; neoplasm; squamous cell carcinoma; human papillomavirus;
D O I
暂无
中图分类号
学科分类号
摘要
Squamous cell carcinoma of the vulva is a disease of significant clinical importance, which arises in the presence or absence of human papillomavirus. We used comparative genomic hybridisation to document non-random chromosomal gains and losses within human papillomavirus positive and negative vulvar cancers. Gain of 3q was significantly more common in human papillomavirus-positive cancers compared to human papillomavirus-negative cancers. The smallest area of gain was 3q22–25, a chromosome region which is frequently gained in other human papillomavirus-related cancers. Chromosome 8q was more commonly gained in human papillomavirus-negative compared to human papillomavirus-positive cancers. 8q21 was the smallest region of gain, which has been identified in other, non-human papillomavirus-related cancers. Chromosome arms 3p and 11q were lost in both categories of vulvar cancer. This study has demonstrated chromosome locations important in the development of vulvar squamous cell carcinoma. Additionally, taken together with previous studies of human papillomavirus-positive cancers of other anogenital sites, the data indicate that one or more oncogenes important in the development and progression of human papillomavirus-induced carcinomas are located on 3q. The different genetic changes seen in human papillomavirus-positive and negative vulvar squamous cell carcinomas support the clinicopathological data indicating that these are different cancer types.
引用
收藏
页码:924 / 928
页数:4
相关论文
共 50 条
  • [41] Detection of copy number variations in melanocytic lesions utilising array based comparative genomic hybridisation
    Ardakani, Nima Mesbah
    Thomas, Carla
    Robinson, Cleo
    Mina, Kym
    Harvey, Nathan Tobias
    Amanuel, Benhur
    Wood, Benjamin Andrew
    PATHOLOGY, 2017, 49 (03) : 285 - 291
  • [42] Microarray-based comparative genomic hybridisation of breast cancer patients receiving neoadjuvant chemotherapy
    Pierga, J-Y
    Reis-Filho, J. S.
    Cleator, S. J.
    Dexter, T.
    MacKay, A.
    Simpson, P.
    Fenwick, K.
    Iravani, M.
    Salter, J.
    Hills, M.
    Jones, C.
    Ashworth, A.
    Smith, I. E.
    Powles, T.
    Dowsett, M.
    BRITISH JOURNAL OF CANCER, 2007, 96 (02) : 341 - 351
  • [43] Genomic differences in benign and malignant follicular thyroid tumours using 1-Mb array-comparative genomic hybridisation
    Qureshi, Abdul A.
    Collins, V. P.
    Jani, P.
    EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2013, 270 (01) : 325 - 335
  • [44] Genomic differences in benign and malignant follicular thyroid tumours using 1-Mb array-comparative genomic hybridisation
    Abdul A. Qureshi
    V. P. Collins
    P. Jani
    European Archives of Oto-Rhino-Laryngology, 2013, 270 : 325 - 335
  • [45] Microarray-based comparative genomic hybridisation of breast cancer patients receiving neoadjuvant chemotherapy
    J-Y Pierga
    J S Reis-Filho
    S J Cleator
    T Dexter
    A MacKay
    P Simpson
    K Fenwick
    M Iravani
    J Salter
    M Hills
    C Jones
    A Ashworth
    I E Smith
    T Powles
    M Dowsett
    British Journal of Cancer, 2007, 96 : 341 - 351
  • [46] Molecular Cytogenetic Characterization of Esophageal Cancer Detected by Comparative Genomic Hybridization
    Chang, Yuli C.
    Yeh, Kun-Tu
    Liu, Ta-Chih
    Chang, Jan-Gowth
    JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2010, 24 (03) : 167 - 174
  • [47] Analysis of genomic aberrations associated with the clinicopathological parameters of rectal cancer by array-based comparative genomic hybridization
    Liang, Jian-Wei
    Shi, Zhi-Zhou
    Zhang, Tong-Tong
    Hao, Jia-Jie
    Wang, Zheng
    Wang, Xiao-Min
    Yang, Hai
    Wang, Ming-Rong
    Zhou, Zhi-Xiang
    Zhang, Yu
    ONCOLOGY REPORTS, 2013, 29 (05) : 1827 - 1834
  • [48] Genetic variation in CD83 and risks of cervical and vulvar cancers: A population-based case-control study
    Bodelon, Clara
    Madeleine, Margaret M.
    Johnson, Lisa G.
    Du, Qin
    Malkki, Mari
    Petersdorf, Effie W.
    Schwartz, Stephen M.
    GYNECOLOGIC ONCOLOGY, 2012, 124 (03) : 525 - 528
  • [49] Genetic differences between HPV-16-containing and -lacking oropharyngeal squamous cell carcinomas detected by comparative genomic hybridization
    Klussmann, P.
    Claessen, S.
    Preuss, S.
    Lehnen, M.
    Weissenborn, S.
    Hopman, A.
    Speel, E. J.
    ORAL ONCOLOGY, 2007, : 203 - 203
  • [50] Comparative genomic hybridisation arrays: High-throughput tools to determine targeted therapy in breast cancer
    Tan, David S. R.
    Reis-Filho, Jorge S.
    PATHOBIOLOGY, 2008, 75 (02) : 63 - 74