Insertional oncogenesis by HPV70 revealed by multiple genomic analyses in a clinically HPV‐negative cervical cancer. Issue 2 (4th September 2019)

• Record Type: Journal Article
• Authors: Van Arsdale, Anne; Patterson, Nicole E.; Maggi, Elaine C.; Agoni, Lorenzo; Van Doorslaer, Koenraad; Harmon, Bryan; Nevadunsky, Nicole; Kuo, Dennis Y.S.; Einstein, Mark H.; Lenz, Jack; Montagna, Cristina
• Is Part Of: Genes, chromosomes & cancer. Volume 59:Issue 2(2020)
• Page Start: 84
• Page End: 95
• Publication Date: 2019-09-04
• Subjects: BCL11B -- cancer -- cervical carcinoma -- fluorescent in situ hybridization -- HPV DNA -- HPV70 -- hybridization capture -- insertional oncogenesis -- long range sequencing -- oncogene; Cancer -- Genetic aspects -- Periodicals; 616.994042
• DOI: 10.1002/gcc.22799
• Languages: English
• ISSNs: 1045-2257

Abstract

Abstract: Cervical carcinogenesis, the second leading cause of cancer death in women worldwide, is caused by multiple types of human papillomaviruses (HPVs). To investigate a possible role for HPV in a cervical carcinoma that was HPV‐negative by PCR testing, we performed HPV DNA hybridization capture plus massively parallel sequencing. This detected a subgenomic, URR‐E6‐E7‐E1 segment of HPV70 DNA, a type not generally associated with cervical cancer, inserted in an intron of the B‐cell lymphoma/leukemia 11B ( BCL11B ) gene in the human genome. Long range DNA sequencing confirmed the virus and flanking BCL11B DNA structures including both insertion junctions. Global transcriptomic analysis detected multiple, alternatively spliced, HPV70‐ BCL11B, fusion transcripts with fused open reading frames. The insertion and fusion transcripts were present in an intraepithelial precursor phase of tumorigenesis. These results suggest oncogenicity of HPV70, identify novel BCL11B variants with potential oncogenic implications, and underscore the advantages of thorough genomic analyses to elucidate insights into HPV‐associated tumorigenesis.