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• W2575837388 abstract "Cervical cancer remains one of the leading causes of cancer-related deaths worldwide. Here we report the extensive molecular characterization of 228 primary cervical cancers, one of the largest comprehensive genomic studies of cervical cancer to date. We observed notable APOBEC mutagenesis patterns and identified SHKBP1, ERBB3, CASP8, HLA-A and TGFBR2 as novel significantly mutated genes in cervical cancer. We also discovered amplifications in immune targets CD274 (also known as PD-L1) and PDCD1LG2 (also known as PD-L2), and the BCAR4 long non-coding RNA, which has been associated with response to lapatinib. Integration of human papilloma virus (HPV) was observed in all HPV18-related samples and 76% of HPV16-related samples, and was associated with structural aberrations and increased target-gene expression. We identified a unique set of endometrial-like cervical cancers, comprised predominantly of HPV-negative tumours with relatively high frequencies of KRAS, ARID1A and PTEN mutations. Integrative clustering of 178 samples identified keratin-low squamous, keratin-high squamous and adenocarcinoma-rich subgroups. These molecular analyses reveal new potential therapeutic targets for cervical cancers." @default.
• W2575837388 created "2017-01-26" @default.
• W2575837388 creator A5025199544 @default.
• W2575837388 creator A5034868991 @default.
• W2575837388 creator A5058191692 @default.
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• W2575837388 date "2017-01-23" @default.
• W2575837388 modified "2023-10-16" @default.
• W2575837388 title "Integrated genomic and molecular characterization of cervical cancer" @default.
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• W2575837388 doi "https://doi.org/10.1038/nature21386" @default.
• W2575837388 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5354998" @default.
• W2575837388 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28112728" @default.
• W2575837388 hasPublicationYear "2017" @default.
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