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EBSCOhost Psychology and Behavioral Sciences Collection
Beschreibungen/Notizen
The Cancer Genome Atlas profiled 279 head and neck squamous cell carcinomas (HNSCCs) to provide a comprehensive landscape of somatic genomic alterations. Here we show that human-papillomavirus-associated tumours are dominated by helical domain mutations of the oncogene
PIK3CA
, novel alterations involving loss of
TRAF3
, and amplification of the cell cycle gene
E2F1
. Smoking-related HNSCCs demonstrate near universal loss-of-function
TP53
mutations and
CDKN2A
inactivation with frequent copy number alterations including amplification of 3q26/28 and 11q13/22. A subgroup of oral cavity tumours with favourable clinical outcomes displayed infrequent copy number alterations in conjunction with activating mutations of
HRAS
or
PIK3CA
, coupled with inactivating mutations of
CASP8
,
NOTCH1
and
TP53
. Other distinct subgroups contained loss-of-function alterations of the chromatin modifier
NSD1
,
WNT
pathway genes
AJUBA
and
FAT1
, and activation of oxidative stress factor
NFE2L2
, mainly in laryngeal tumours. Therapeutic candidate alterations were identified in most HNSCCs.
The Cancer Genome Atlas presents an integrative genome-wide analysis of genetic alterations in 279 head and neck squamous cell carcinomas (HNSCCs), which are classified by human papillomavirus (HPV) status; alterations in
EGFR
,
FGFR
,
PIK3CA
and cyclin-dependent kinases are shown to represent candidate targets for therapeutic intervention in most HNSCCs.
Large-scale analysis of head and neck cancers
Squamous cell head and neck cancer is one of the most common and deadly cancers. Despite initial responses to combinations of surgery, radiation and chemotherapy, approximately half of all tumours recur, usually within two years of initial diagnosis. Molecular markers and targeted therapies have had little impact on this disease to date. Here, The Cancer Genome Atlas team presents a detailed genome-wide overview of alterations and highlights critical genetic events of potential biological and clinical significance in head and neck squamous cell carcinomas (HNSCCs) with different human papillomavirus status. Mutational profiles reveal distinct subgroups of HNSCCs. Mutations in EGFR, FGFRs, PIK3CA and cyclin-dependent kinases represent candidate targets for therapeutic intervention in the majority of HNSCCs.