High-risk human papillomaviruses (HPVs) are etiological agents of cervical cancer, the second most common cause of cancer death in women worldwide and are also associated with a number of other anogenital tract carcinomas, including, anal, vulvar and penile cancers as well as approximately 20% of oral cancers, particularly oropharyngeal carcinomas. Due to the long latency period between the initial HPV infection and cancer development, It will be decades, however, before a recently introduced prophylactic vaccine that is to prevent new infections by the two most common high-risk HPVs will have a significant impact on the incidence and mortality of HPV associated cancers. Till then, 10 women will die of HPV associated cervical cancer every day in the US, alone. HPV-associated carcinogenesis is driven by viral E6/E7 oncoprotein expression;these proteins not only contribute to induction of premalignant lesions, but also mechanistically contribute to malignant progression. We have shown that the HPV E7 oncoprotein causes epigenetic reprogramming of HPV infected cells by causing a dramatic decrease in trimethylation of lysine residue 27 of histone H3. Since lysine 27 trimethylation of histone H3 marks silenced chromatin, erasing this mark causes increased expression of genes that are normally silenced in epithelial cells. Such genes include the tumor suppressor and cervical cancer biomarker p16INK4A, as well as many homeobox genes that are critical for cell fate determination and organismal development. This project is focused on investigating mechanisms and biological consequences of HPV16 E7 induced epigenetic reprogramming.
Aim 1 is to determine the mechanism by which HPV16 E7 expression causes increased expression of the two enzymes, JMJD3 and UTX, which remove the repressive trimethyl mark on lysine 27 of histone H3.
Aim 2 is to determine the biological consequences of increased JMMJD3 and UTX expression in HPV expressing epithelial cells.
Aim 3 is to determine the biological consequences of E7 mediated disruption of E2F6 containing polycomb repressive complexes and increased expression of the histone methyl transferase and oncoprotein, EZH2, in HPV16 E7 expressing epithelial cells. Since, in contrast to somatic mutations, epigenetic reprogramming is potentially reversible by small molecule inhibitors of the corresponding histone modifying enzymes, these studies may have therapeutic implications for HPV-associated lesions and cancers.

Public Health Relevance

Infections with high-risk human papillomaviruses (HPVs) have been linked to a number of human cancers, including almost all cervical carcinomas. Despite a recently introduced prophylactic vaccine, more than 10 women will die from HPV-associated cervical carcinoma every day in the US alone, for the next several decades. The focus of this proposal is to determine the molecular mechanisms of HPV16-induced reprogramming of cell identity and how this contributes to tumor development.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA066980-17
Application #
8225223
Study Section
Special Emphasis Panel (ZRG1-IDM-P (02))
Program Officer
Read-Connole, Elizabeth Lee
Project Start
1996-04-19
Project End
2015-02-28
Budget Start
2012-03-01
Budget End
2013-02-28
Support Year
17
Fiscal Year
2012
Total Cost
$405,472
Indirect Cost
$167,322
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code
02115
McBride, Alison A; Münger, Karl (2018) Expert Views on HPV Infection. Viruses 10:
Liu, Zhiyi; Pouli, Dimitra; Alonzo, Carlo A et al. (2018) Mapping metabolic changes by noninvasive, multiparametric, high-resolution imaging using endogenous contrast. Sci Adv 4:eaap9302
Chiang, Cindy; Pauli, Eva-Katharina; Biryukov, Jennifer et al. (2018) The Human Papillomavirus E6 Oncoprotein Targets USP15 and TRIM25 To Suppress RIG-I-Mediated Innate Immune Signaling. J Virol 92:
Gaglia, Marta M; Munger, Karl (2018) More than just oncogenes: mechanisms of tumorigenesis by human viruses. Curr Opin Virol 32:48-59
Meyers, Jordan M; Grace, Miranda; Uberoi, Aayushi et al. (2018) Inhibition of TGF-? and NOTCH Signaling by Cutaneous Papillomaviruses. Front Microbiol 9:389
Sharma, Surendra; Munger, Karl (2018) Expression of the cervical carcinoma expressed PCNA regulatory (CCEPR) long noncoding RNA is driven by the human papillomavirus E6 protein and modulates cell proliferation independent of PCNA. Virology 518:8-13
Wallace, Nicholas A; Münger, Karl (2018) The curious case of APOBEC3 activation by cancer-associated human papillomaviruses. PLoS Pathog 14:e1006717
Miller, Anna K; Munger, Karl; Adler, Frederick R (2017) A Mathematical Model of Cell Cycle Dysregulation Due to Human Papillomavirus Infection. Bull Math Biol 79:1564-1585
Harden, Mallory E; Prasad, Nripesh; Griffiths, Anthony et al. (2017) Modulation of microRNA-mRNA Target Pairs by Human Papillomavirus 16 Oncoproteins. MBio 8:
Grace, Miranda; Munger, Karl (2017) Proteomic analysis of the gamma human papillomavirus type 197 E6 and E7 associated cellular proteins. Virology 500:71-81

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