Comparative evaluation of genetic assays to identify oral pre-cancerous fields

被引:28
作者
Bremmer, Jantine F. [4 ]
Braakhuis, Boudewijn J. M. [2 ]
Brink, Arjen [2 ,4 ]
Broeckaert, Mark A. M. [3 ]
Belien, Jeroen A. M. [3 ]
Meijer, Gerrit A. [3 ]
Kuik, Dirk J. [1 ]
Leemans, C. Rene [2 ]
Bloemena, Elisabeth [3 ]
van der Waal, Isaac [4 ]
Brakenhoff, Ruud H. [1 ,2 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, Dept Otolaryngol Head Neck Surg, NL-1007 MB Amsterdam, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, Dept Pathol, NL-1007 MB Amsterdam, Netherlands
[3] Vrije Univ Amsterdam Med Ctr, Dept Clin Epidemiol & Biostat, NL-1007 MB Amsterdam, Netherlands
[4] Vrije Univ Amsterdam Med Ctr, Dept Oromaxillofacial Surg & Oral Pathol, NL-1007 MB Amsterdam, Netherlands
关键词
DNA ploidy; field cancerization; leukoplakia; loss of heterozygosity; MLPA;
D O I
10.1111/j.1600-0714.2008.00682.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
BACKGROUND: Oral squamous cell carcinomas often develop in a pre-cancerous field, defined as mucosal epithelium with cancer-related genetic alterations, and which may appear as a clinically visible lesion. The test characteristics of three genetic assays that were developed to detect pre-cancerous fields were investigated and compared to histology. METHODS: In total, 10 pre-cancerous fields that were not visible at clinical inspection and gave rise to malignant transformation based on an identical TP53 mutation in tumor and mucosal epithelium in the surgical margin, as well as 10 normal oral mucosa specimens were analyzed for numerical chromosomal changes with multiplex ligation-dependent probe amplification (MLPA), for loss of heterozygosity (LOH), with microsatellite PCR and for DNA index alterations with DNA image analysis. RESULTS: No alterations were detected in normal tissue by either of the assays. Both MLPA and LOH assays detected all pre-cancerous fields. DNA cytometry identified aneuploidy in four of 10 pre-cancerous fields, while the corresponding tumors that developed in these fields were shown to be aneuploid. CONCLUSIONS: Both the MLPA and LOH assay seem suitable for screening pre-cancerous fields in subjects at high risk for oral cancer even in the absence of clinically abnormal appearing oral mucosa. Measurements of DNA index might be valuable to determine the time to progression. J Oral Pathol Med (2008) 37: 599-606
引用
收藏
页码:599 / 606
页数:8
相关论文
共 37 条
  • [2] [Anonymous], COCHRANE DATABASE SY
  • [3] Interlaboratory reproducibility of semiautomated cell cycle analysis of flow cytometric DNA-histograms obtained from fresh material of 1,295 breast cancer cases
    Bergers, E
    Montironi, R
    vanDiest, PJ
    Prete, E
    Baak, JPA
    [J]. HUMAN PATHOLOGY, 1996, 27 (06) : 553 - 560
  • [4] BOCKING A, 1995, ANAL QUANT CYTOL, V17, P1
  • [5] Braakhuis BJM, 2003, CANCER RES, V63, P1727
  • [6] A noninvasive genetic screening test to detect oral preneoplastic lesions
    Bremmer, JF
    Braakhuis, BJM
    Ruijter-Schippers, HJ
    Brink, A
    Duarte, HMB
    Kuik, DJ
    Bloemena, E
    Leemans, CR
    van der Waal, IC
    Brakenhoff, RH
    [J]. LABORATORY INVESTIGATION, 2005, 85 (12) : 1481 - 1488
  • [7] Copy-number methods dramatically underestimate loss of heterozygosity in cancer
    Calhoun, Eric S.
    Gallmeier, Eike
    Cunningham, Steven C.
    Eshleman, James R.
    Hruban, Ralph H.
    Kern, Scott E.
    [J]. GENES CHROMOSOMES & CANCER, 2006, 45 (11) : 1070 - 1071
  • [8] A systematic review of measures of effectiveness in screening for oral cancer and precancer
    Downer, Martin C.
    Moles, David R.
    Palmer, Stephen
    Speight, Paul M.
    [J]. ORAL ONCOLOGY, 2006, 42 (06) : 551 - 560
  • [9] Medical progress - Head and neck cancer
    Forastiere, A
    Koch, W
    Trotti, A
    Sidransky, D
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (26) : 1890 - 1900
  • [10] METHOD FOR ANALYSIS OF CELLULAR DNA CONTENT OF PARAFFIN-EMBEDDED PATHOLOGICAL MATERIAL USING FLOW-CYTOMETRY
    HEDLEY, DW
    FRIEDLANDER, ML
    TAYLOR, IW
    RUGG, CA
    MUSGROVE, EA
    [J]. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1983, 31 (11) : 1333 - 1335