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Zbornik - Društvo genetičara Srbije

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226 ZBORNIK ABSTRAKATA III KONGRESA GENETIÈARA SRBIJE V-Pos-23<br />

Subotica, 30. novembar - 4. decembar 2004.<br />

KORELACIJA INFEKCIJE VISOKORIZIÈNIM HUMANIM<br />

PAPILOMA VIRUSIMA SA TOKOM BOLESTI U BOLESNIKA SA ORALNIM<br />

KARCINOMU USNE DUPLJE<br />

Z. Magiæ 1 , N. Joviæ 2 , R. Kozomara 2 i J. Stojanoviæ 1<br />

1<br />

Institut za medicinska istraivanja, Vojnomedicinska akademija, Beograd<br />

2<br />

Klinika za maksilofacijalnu hirurgiju, Vojnomedicinska akademija, Beograd<br />

Analizirano je 50 pacijenata u II i III stadijumu OSCC jezika i poda usne duplje<br />

(histološki i nuklearni gradus 1, 2 i 3). Starost pacijenata se kretala od 45 do 72 godine,<br />

97% su bili pušaèi dok je 93% konzumiralo alkohol. DNK iz tumorskog tkiva je<br />

izolovana fenol-hloroformskom ekstrakcijom. Prisustvo visokoriziènih tipova HPV (16,<br />

18, 31 i 33) je detktovano PCR-om i PAGE-om. HPV infekcija je detktovana kod 64%<br />

pacijenata. HPV16 je detektovan kod 10 pacijenata (31.2%), HPV18 i HPV31 kod 6<br />

(18.7%), dok HPV33 nije detektovan. Kod 3 pacijenta (9.3%) su detektovani<br />

istovremeno HPV16 i HPV31 a HPV18 i HPV31 kod 7 (21%). Tumori u III klinièkom<br />

stadijumu su u 58% sluèajeva sadrali neki od ispitivanih virusa. Umereno-diferentovani<br />

OSCC sa srednjim nuklearnim gradusom su najèešæe bili inficirani sa HPV (46.8%),<br />

dobro diferentovani 40.6%, a slabo-difrentovani svega 12.5%. Distribucija HPV<br />

infekcije u tumorima niskog nuklearnog gradusa (28.1%) i visokog nuklearnog gradusa<br />

(25%) je bila slièna. Pušenje i konzumacija alkohola su zavisni prediktivni faktor HPV<br />

infekcije. Period bez pojave bolesti (DFI) u ispitivanoj grupi pacijenata se kretao od 4 do<br />

36 meseci. DFI i ukupno preivljavanje (OS) kod pacijenata sa HPV infekcijom su bili<br />

znaèajno kraæi u odnosu na pacijente bez HPV infekcije (log rank test). Karcinomi usne<br />

duplje su èesto inficirani kancerogenim tipovima HPV. U ispitivanoj grupi pacijenata<br />

napena je znaèajna povezanost infekcije tumora kancerogenim tipovima HPV sa tokom i<br />

prognozom bolesti.<br />

CORRELATION OF HIGH RISK HUMAN PAPILLOMAVIRUS INFECTION<br />

WITH DISEASE PROGRESSION IN PATIENTS WITH ORAL<br />

SQUAMOCELLULAR CARCINOMA<br />

We analysed 50 patients with stage II and III of hystologically confirmed OSCC of the<br />

tonguae or oral floor (hystological and nucler grade 1, 2 or 3). Patients were 45-72 years<br />

old, 97% were heavy smokers, 93% were alcochol consumers. Genomicic DNA was isolated<br />

according to standard procedure with phenol/chloroform/isoamilalcohol. Presence<br />

of HPV types 16, 18, 31 and 33 was detected by PCR/PAGE. HPV infection was detected<br />

in 64% of patients. HPV16 was found in 10 pts (31.2%), HPV18 and HPV31 in 6<br />

(18.7%) and none with HPV33. Double positeve HPV infection HPV16+31 was detected<br />

in 3 patients (9.3%) and HPV18+31 in 7 patients (21%). Tumors in clinical stage III was<br />

more likely to contain HPV (58%). Moderately-differentiated OSCC with medium-nuclear<br />

grade were more likely to contain HPV (46.8%), well-differentiated to (40.6%) and<br />

poorly- differentiated in only (12.5%). Low-nuclear grade was detected in 28.1% and<br />

high-nuclear grade in 25% HPV positive tumors. Tobaco usage and alcochol consumption<br />

were an dependent predictor of HPV risk for OSCC. Disease-free interval (DFI) of<br />

patients ranged from 4 to 36 months. DFI and overall survival (OS) in pts with HPV infection<br />

compared to the pts without HPV infection was significantly shorter (log rank<br />

test). Infection with oncogenic HPV is frequent in oral cancers. Viral oncogene expression<br />

and viral integration suggest firm correlation between HPV infection and clinical<br />

course of disease in the examined grouop of patients.

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