Chromosomal instability, aneuploidy and routine high-resolution DNA content analysis in oral cancer risk evaluation

被引:1
作者
Giaretti, Walter [1 ]
Pentenero, Monica [2 ]
Gandolfo, Sergio [2 ]
Castagnola, Patrizio [1 ]
机构
[1] IRCCS AOU San Martino IST, Dept Diagnost Oncol, Biophys & Cytometry Sect, I-16132 Genoa, Italy
[2] Univ Turin, Oral Med & Oral Oncol Sect, Dept Clin & Biol Sci, I-10043 Turin, TO, Italy
关键词
aneuploidy; chromosomal instability; DNA flow cytometry; DNA image cytometry; oral cancer; oral 'field cancerization'; theory; oral potentially malignant disorders; SQUAMOUS-CELL CARCINOMA; FLOW-CYTOMETRIC ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; POTENTIALLY MALIGNANT LESIONS; GENETICALLY ALTERED FIELDS; PARAFFIN-EMBEDDED TISSUE; NF-KAPPA-B; PREMALIGNANT LESIONS; EPITHELIAL DYSPLASIA; NECK-CANCER;
D O I
10.2217/FON.12.116
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Carcinogen exposure of the oral cavity is thought to create an extensive 'field cancerization'. According to this model, a very early precursor of oral cancer is a patch of normal-appearing mucosa in which stem cells share genetic/genomic aberrations. These precancerous fields then become clinically visible as white and red lesions (leuko- and erythro-plakias), which represent the vast majority of the oral potentially malignant disorders. This review focuses on aneuploidy (where it is from) and on biomarkers associated with DNA aneuploidy in oral mucosa and oral potentially malignant disorders, as detected by DNA image and flow cytometry. Data from the literature strongly support the association of DNA ploidy with dysplasia. However, work is still needed to prove the clinical value of DNA ploidy in large-scale prospective studies. Using high-resolution DNA flow cytometry with fresh/frozen material and the degree of DNA aneuploidy (DNA Index) might improve the prediction of risk of oral cancer development.
引用
收藏
页码:1257 / 1271
页数:15
相关论文
共 151 条
  • [1] The flow cytometric analysis of premalignant and malignant lesions in head and neck squamous cell carcinoma
    Abou-Elhamd, Kamal-Eldin Ahmed
    Habib, Tito Naeem
    [J]. ORAL ONCOLOGY, 2007, 43 (04) : 366 - 372
  • [2] Genomic microarrays in human genetic disease and cancer
    Albertson, DG
    Pinkel, D
    [J]. HUMAN MOLECULAR GENETICS, 2003, 12 : R145 - R152
  • [3] Oral field cancerization: Current evidence and future perspectives
    Punnya V. Angadi
    J. K. Savitha
    Sanjay S. Rao
    Y. Sivaranjini
    [J]. Oral and Maxillofacial Surgery, 2012, 16 (2) : 171 - 180
  • [4] [Anonymous], CA CANC J CLIN, DOI DOI 10.3322/CAAC.20107
  • [5] [Anonymous], 2012, MITELMAN DATABASE CH
  • [6] Telomeres and telomerase in cancer
    Artandi, Steven E.
    DePinho, Ronald A.
    [J]. CARCINOGENESIS, 2010, 31 (01) : 9 - 18
  • [7] Genome stability is ensured by temporal control of kinetochore-microtubule dynamics
    Bakhoum, Samuel F.
    Thompson, Sarah L.
    Manning, Amity L.
    Compton, Duane A.
    [J]. NATURE CELL BIOLOGY, 2009, 11 (01) : 27 - U51
  • [8] Chromatid cohesion defects may underlie chromosome instability in human colorectal cancers
    Barber, Thomas D.
    McManus, Kirk
    Yuen, Karen W. Y.
    Reis, Marcelo
    Parmigiani, Giovanni
    Shen, Dong
    Barrett, Irene
    Nouhi, Yasaman
    Spencer, Forrest
    Markowitz, Sanford
    Velculescu, Victor E.
    Kinzler, Kenneth W.
    Vogelstein, Bert
    Lengauer, Christoph
    Hieter, Philip
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (09) : 3443 - 3448
  • [9] Barnes L., 2005, World Health Organization classification of tumours, pathology and genetics of head and neck tumours
  • [10] BERLINGER NT, 1987, ARCH OTOLARYNGOL, V113, P1301