Journal Article DKFZ-2019-02023

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Absence of disruptive TP53 mutations in high-risk human papillomavirus-driven neck squamous cell carcinoma of unknown primary.

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2019
Wiley Interscience New York, NY [u.a.]

Head & neck 41(11), 3833-3841 () [10.1002/hed.25915]
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Abstract: To enforce the evidence for causality between high-risk human papillomavirus (hrHPV) infections and neck squamous cell carcinoma from unknown primary (NSCCUP) and provide biological basis for treatment de-intensification, we searched for TP53 mutations in association with HPV status.TP53 mutations were searched for by amplification of exons 4 to 10.Of the 70 NSCCUP, 27 (39%) harbored HPV infection. TP53 sequencing resulted in the identification of 19 patients harboring single mutations including 16 disruptive alterations (84%). The association of TP53 mutations and HPV could be evaluated in 48 NSCCUP including those with disruptive mutation in any exon (n = 16) and those without mutations but with complete sequence of exons 4 to 9 (n = 32): no disruptive mutations were found in the 17 HPV-driven NSCCUP but in 16 of the 31 non-HPV-driven NSCCUP (P = .0002).In a fraction of cases, NSCCUP is an HPV-driven entity harboring wild-type TP53 gene or nondisruptive TP53 mutations. HPV-driven NSCCUP might benefit from treatment de-intensification.

Classification:

Note: Head Neck. 2019 Nov;41(11):3833-3841

Contributing Institute(s):
  1. Infektionen und Krebs-Epidemiologie (F022)
  2. Infektionen und Krebs-Epidemiologie (F020)
  3. Molekulare Grundlagen von HNO-Tumoren (A102)
Research Program(s):
  1. 319H - Addenda (POF3-319H) (POF3-319H)

Appears in the scientific report 2019
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Medline ; BIOSIS Previews ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; IF < 5 ; JCR ; NCBI Molecular Biology Database ; NationallizenzNationallizenz ; SCOPUS ; Science Citation Index ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2019-08-22, last modified 2024-02-29



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