2001
DOI: 10.1002/1097-0142(20010815)92:4<805::aid-cncr1386>3.0.co;2-9
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Human papillomavirus positive squamous cell carcinoma of the oropharynx

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Cited by 424 publications
(399 citation statements)
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References 33 publications
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“…In this study, we found an HPV prevalence of 24.3% in our cohort, which is lower than the prevalence in OSCC and tonsillar cancer reported for the USA (45-83%) 4,5 or northern Europe (26-93%), 5,23,24 but comparable to data for central Europe (14-33%) [25][26][27] . We considered HPV-association of samples when high risk HPV-DNA was detected along with p16INK4a expression.…”
Section: Discussioncontrasting
confidence: 70%
“…In this study, we found an HPV prevalence of 24.3% in our cohort, which is lower than the prevalence in OSCC and tonsillar cancer reported for the USA (45-83%) 4,5 or northern Europe (26-93%), 5,23,24 but comparable to data for central Europe (14-33%) [25][26][27] . We considered HPV-association of samples when high risk HPV-DNA was detected along with p16INK4a expression.…”
Section: Discussioncontrasting
confidence: 70%
“…In contrast and as observed in our study, p53 is frequently upregulated in HPVnegative tumors due to mutations in the TP53 gene as a result of exposure to tobacco and/or alcohol. 10,16,20,27,47 Although p21 Cip1/WAF1 is known to be a downstream effector of p53, 48,49 it was surprising to find overexpression in HPV-positive tumors harboring low or no detectable levels of p53. Such observations have also been reported by Milde-Langosch et al 50 in HPV-associated uterine cervical tumors and suggest that also p53-independent mechanisms may lead to p21 Cip1/WAF1 accumulation as described previously.…”
Section: Discussionmentioning
confidence: 99%
“…26 This may have a strong effect on survival, because it has been indicated that tumors with intact p53 are still capable of inducing apoptosis in response to radiation therapy, which results in a favorable clinical outcome. 27 This study was undertaken to investigate the expression of key cell cycle proteins in the pRb pathway (p16 INK4A cyclin D1, p27 Kip1 pRb) and the p53 cascade (p14 ARF MDM2, p53 and p21 Cip1/WAF1 ), using a series of 77 tonsillar squamous cell carcinomas for which the HPV16 status and the clinical follow-up data were available. Tonsillar squamous cell carcinomas show the highest prevalence of oncogenic HPV and are thus ideally suited to search for molecular and clinicopathological differences induced by either HPV, or tobacco and alcohol consumption.…”
mentioning
confidence: 99%
“…39,40 In a review on epidemiologic and molecular bases, Ha and Califano 41 attrib- uted to HR HPV a role in oral carcinogenesis but only in a small subset of cases, with differences reported in clinical outcome, response to radiotherapy and prognosis. 21,22,33,[42][43][44][45] In this context, it becomes important to identify this cluster principally on the basis of key immunohistochemical cell cycle markers that are inexpensive and reliable, such as PCNA, MIB-1 and survivin. Several reports have focused on the identification of useful markers such as molecules involved in the proliferation pathway or in the regulation of apoptosis, which may influence the cell death/cell viability balance toward cell proliferation or cancer.…”
Section: Discussionmentioning
confidence: 99%