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Rev Fac Odon<strong>to</strong>l Bauru2002; 10(2):63-7(LOH), which may conta<strong>in</strong> putative tumoursupressor genes <strong>in</strong> <strong>oral</strong>, oropharyngeal, and otherhead and neck cancers 25 .Follow<strong>in</strong>g the pioneer studies by Partridge andcolleagues 14 , deletions <strong>in</strong> the long arm ofchromosome 3 <strong>in</strong> <strong>oral</strong> cancer has now beenhighlighted as a very common event, occurr<strong>in</strong>g <strong>in</strong>approximately 70% of all SCC 15 . Furthermore, itwas shown that allelic imbalance or LOH <strong>in</strong> 3p werepresent <strong>in</strong> dysplastic mucosa but not <strong>in</strong> normalmucosa and, therefore, an early event <strong>in</strong> the processof carc<strong>in</strong>ogenesis 5 . In potential malignancies,deletions of 3p were rather frequent, especially whendysplasias recurred, or when SCC developed. 3pdeletions thus might serve as a biomarker <strong>to</strong> identifylesions that may relapse or even undergo malignantchange 32 . Moreover, it has been demonstrated thatif one <strong>in</strong>troduced an <strong>in</strong>tact human chromosome 3<strong>in</strong><strong>to</strong> different tumorigenic <strong>cell</strong> l<strong>in</strong>es, tumourigenicitywould be suppressed <strong>in</strong> each <strong>cell</strong> l<strong>in</strong>e, with significantdecrease <strong>in</strong> <strong>in</strong> vitro growth rate and morphologicchanges 24 .Loss of loci <strong>in</strong> chromosome 9p and amplificationof 11q have also been related <strong>to</strong> SCC of head andneck. However, no reports have been found <strong>in</strong>potentially malignant lesions. Both have shownstrik<strong>in</strong>g prognostic value for cancer rather than<strong>predict</strong>ive of development of cancer.Image-based ploidy analysisVery recently image-based ploidy analysis hasbeen shown highly effective <strong>to</strong> <strong>predict</strong> malignanttransformation with high sensitivity and specificityand can be applied rout<strong>in</strong>ely <strong>to</strong> biopsy samples <strong>in</strong> ahospital sett<strong>in</strong>g.Cumulative evidence po<strong>in</strong>ts <strong>to</strong> abnormalities <strong>in</strong>the number of chromosomes (aneuploidy) as a causerather than a consequence of malignanttransformation 21 . Notwithstad<strong>in</strong>g this, consider<strong>in</strong>gthat cancer and genetic <strong>in</strong>stability are almostsynonyms, mutations <strong>in</strong> genes that control segregationof chromosomes dur<strong>in</strong>g mi<strong>to</strong>sis and/or centrosomalaberrations are critical <strong>to</strong> determ<strong>in</strong>e malignantchange. As a matter of fact, aberrant chromosomalsegregation occur exclusively <strong>in</strong> aneuploid tumour<strong>cell</strong>l<strong>in</strong>es, caus<strong>in</strong>g, therefore, aberration of DNAcontent (ploidy) <strong>to</strong> play an essential role oncarc<strong>in</strong>ogenesis 21, 22 .A Norwegian study has recently revealed whatappears <strong>to</strong> be the first successful attempt <strong>to</strong> establisha methodology for prognostication of potentiallymalignant lesions of the <strong>oral</strong> mucosa. One hundredand fifty patients with an <strong>in</strong>itial diagnosis ofleukoplakia had their lesions analyzed by image-basedploidy and were followed up for 9 years. Out of the27 aneuploid lesions, 21 underwent malignanttransformation. From the 20 tetraploid lesions, 12changed <strong>in</strong><strong>to</strong> the malignant phenotype, whilst only 3out of the 103 diploid lesions became malignant 21 .Although DNA ploidy measurements by imagecy<strong>to</strong>metry is a very crude method, with a coefficien<strong>to</strong>f variation of 3-5%, which translates <strong>to</strong> 1-2chromosomes per nucleus, the long follow-up timepresented <strong>in</strong> this study supports the notion that DNAcontent is a highly sensitive and a specific markerfor <strong>predict</strong><strong>in</strong>g the subsequent occurrence of an <strong>oral</strong><strong>squamous</strong> <strong>cell</strong> <strong>carc<strong>in</strong>oma</strong> 22 .ACKNOWLEDGEMENTSThe authors are thankfull <strong>to</strong> Dr. Jonathan Millerfor DNA image (www.jonathanpmiller.com) and Dr.Patrick O. Brown (Howard Hughes MedicalInstitute - Stanford University) for DNA microchipimage. The images are illustrate <strong>in</strong> the front page ofthis journal.RESUMOInúmeras tentativas têm sido feitas paraestabelecer ou mesmo desenvolver marcadores paradeterm<strong>in</strong>ar a susceptibilidade de tecidoshis<strong>to</strong>logicamente normais sofrerem transformaçãomaligna. A literatura é extremamente vasta noassun<strong>to</strong>, mui<strong>to</strong> embora um marcador def<strong>in</strong>itivo parao <strong>carc<strong>in</strong>oma</strong> de boca a<strong>in</strong>da não tenha sidoestabelecido. Os <strong>in</strong>dicadores atuais podem sersubdivididos em morfológicos (cl<strong>in</strong>ico-pa<strong>to</strong>lógico) emoleculares (serológicos/salivares e genômicos).Dentre eles, destacam-se o p53 tan<strong>to</strong> no soro comono sítio da lesão, a deleção de porções do gene 3p e,mais recentemente, a análise de ploidia baseada emimagem. Embora <strong>to</strong>dos sejam cientificamenteobje<strong>to</strong>s de muita pesquisa e resultadosespeculatórios, a ploidia baseada em imagem pareceser o mé<strong>to</strong>do mais sensível e confiável para prevertransformação maligna em lesões cancerizáveis damucosa bucal.UNITERMOS: Lesões cancerizáveis;Marcadores tumorais; Carc<strong>in</strong>oma esp<strong>in</strong>o-celular;Análise de ploidia por imagem; Câncer, prevenção.65

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