Literature DB >> 32631904

The D2 and D3 Sublineages of Human Papilloma Virus 16-Positive Cervical Cancer in Guatemala Differ in Integration Rate and Age of Diagnosis.

Hong Lou1, Joseph F Boland1, Edmundo Torres-Gonzalez2, Anaseidy Albanez3, Weiyin Zhou1, Mia K Steinberg1, Lena Diaw2, Jason Mitchell1, David Roberson1, Michael Cullen1, Lisa Garland1, Sara Bass1, Robert D Burk4, Meredith Yeager1, Nicolas Wentzensen5, Mark Schiffman5, Enrique Alvirez Freites6,7, Eduardo Gharzouzi8, Lisa Mirabello5, Michael Dean9.   

Abstract

Human papillomavirus (HPV) 16 displays substantial sequence variation; four HPV16 lineages (A, B, C, and D) have been described as well as multiple sublineages. To identify molecular events associated with HPV16 carcinogenesis, we evaluated viral variation, the integration of HPV16, and somatic mutation in 96 cervical cancer samples from Guatemala. A total of 65% (62/96) of the samples had integrated HPV16 sequences and integration was associated with an earlier age of diagnosis and premenopausal disease. HPV16 integration sites were broadly distributed in the genome, but in one tumor, HPV16 integrated into the promoter of the IFN regulatory factor 4 (IRF4) gene, which plays an important role in the regulation of the IFN response to viral infection. The HPV16 D2 and D3 sublineages were found in 23% and 30% of the tumors, respectively, and were significantly associated with adenocarcinoma. D2-positive tumors had a higher rate of integration, earlier age of diagnosis, and a lower rate of somatic mutation, whereas D3-positive tumors were less likely to integrate, had later age of diagnosis, and exhibited a higher rate of somatic mutation. In conclusion, Guatemalan cervical tumors have a high frequency of very high-risk HPV16 D2 and D3 sublineages harboring distinct histology, which may help guide future therapeutic strategies to target the tumor and reduce recurrence. SIGNIFICANCE: This study details the biological and molecular properties of the most pathogenic forms of HPV16, the cause of the majority of cervical cancers. ©2020 American Association for Cancer Research.

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Year:  2020        PMID: 32631904      PMCID: PMC7501218          DOI: 10.1158/0008-5472.CAN-20-0029

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  41 in total

Review 1.  Papillomavirus genome structure, expression, and post-transcriptional regulation.

Authors:  Zhi-Ming Zheng; Carl C Baker
Journal:  Front Biosci       Date:  2006-09-01

2.  Human papillomavirus type 16 and 18 variants: race-related distribution and persistence.

Authors:  Long Fu Xi; Nancy B Kiviat; Allan Hildesheim; Denise A Galloway; Cosette M Wheeler; Jesse Ho; Laura A Koutsky
Journal:  J Natl Cancer Inst       Date:  2006-08-02       Impact factor: 13.506

3.  Genome Analysis of Latin American Cervical Cancer: Frequent Activation of the PIK3CA Pathway.

Authors:  Hong Lou; Guillermo Villagran; Joseph F Boland; Kate M Im; Sarita Polo; Weiyin Zhou; Ushie Odey; Eligia Juárez-Torres; Ingrid Medina-Martínez; Edgar Roman-Basaure; Jason Mitchell; David Roberson; Julie Sawitzke; Lisa Garland; Maria Rodríguez-Herrera; David Wells; Jennifer Troyer; Francisco Castillo Pinto; Sara Bass; Xijun Zhang; Miriam Castillo; Bert Gold; Hesler Morales; Meredith Yeager; Jaime Berumen; Enrique Alvirez; Eduardo Gharzouzi; Michael Dean
Journal:  Clin Cancer Res       Date:  2015-06-16       Impact factor: 12.531

4.  The E7 oncoprotein is translated from spliced E6*I transcripts in high-risk human papillomavirus type 16- or type 18-positive cervical cancer cell lines via translation reinitiation.

Authors:  Shuang Tang; Mingfang Tao; J Philip McCoy; Zhi-Ming Zheng
Journal:  J Virol       Date:  2006-05       Impact factor: 5.103

5.  Integration of human papillomavirus type 16 into the human genome correlates with a selective growth advantage of cells.

Authors:  S Jeon; B L Allen-Hoffmann; P F Lambert
Journal:  J Virol       Date:  1995-05       Impact factor: 5.103

6.  Epidemiologic classification of human papillomavirus types associated with cervical cancer.

Authors:  Nubia Muñoz; F Xavier Bosch; Silvia de Sanjosé; Rolando Herrero; Xavier Castellsagué; Keerti V Shah; Peter J F Snijders; Chris J L M Meijer
Journal:  N Engl J Med       Date:  2003-02-06       Impact factor: 91.245

7.  Genomic characterization of viral integration sites in HPV-related cancers.

Authors:  Clara Bodelon; Michael E Untereiner; Mitchell J Machiela; Svetlana Vinokurova; Nicolas Wentzensen
Journal:  Int J Cancer       Date:  2016-07-15       Impact factor: 7.396

8.  HPV16 E7 Genetic Conservation Is Critical to Carcinogenesis.

Authors:  Lisa Mirabello; Meredith Yeager; Kai Yu; Gary M Clifford; Yanzi Xiao; Bin Zhu; Michael Cullen; Joseph F Boland; Nicolas Wentzensen; Chase W Nelson; Tina Raine-Bennett; Zigui Chen; Sara Bass; Lei Song; Qi Yang; Mia Steinberg; Laurie Burdett; Michael Dean; David Roberson; Jason Mitchell; Thomas Lorey; Silvia Franceschi; Philip E Castle; Joan Walker; Rosemary Zuna; Aimée R Kreimer; Daniel C Beachler; Allan Hildesheim; Paula Gonzalez; Carolina Porras; Robert D Burk; Mark Schiffman
Journal:  Cell       Date:  2017-09-07       Impact factor: 41.582

9.  HPV16 genetic variation and the development of cervical cancer worldwide.

Authors:  I Cornet; T Gheit; M R Iannacone; J Vignat; B S Sylla; A Del Mistro; S Franceschi; M Tommasino; G M Clifford
Journal:  Br J Cancer       Date:  2012-11-20       Impact factor: 7.640

10.  Evolution and taxonomic classification of human papillomavirus 16 (HPV16)-related variant genomes: HPV31, HPV33, HPV35, HPV52, HPV58 and HPV67.

Authors:  Zigui Chen; Mark Schiffman; Rolando Herrero; Rob Desalle; Kathryn Anastos; Michel Segondy; Vikrant V Sahasrabuddhe; Patti E Gravitt; Ann W Hsing; Robert D Burk
Journal:  PLoS One       Date:  2011-05-27       Impact factor: 3.240

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