Combined Effect on HIV and HPV in Oral Cancer
Combined Effect on HIV and HPV in Oral Cancer
批准号:
7897929
负责人:
Reuben Han-Kyu Kim
金额:
$11.8万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-09-01 至 2012-07-31
关键词:
AccountingAcquired Immunodeficiency SyndromeAddressAdultApoptosisBiologicalCD4 Lymphocyte CountCarcinogensCell Cycle RegulationCellsCervicalChildDNA DamageDental General PracticeDevelopmentEarly DiagnosisExhibitsFemaleGene ProteinsGeneticGenomeGoalsHIVHPV-High RiskHead and Neck CancerHighly Active Antiretroviral TherapyHumanHuman PapillomavirusHuman papilloma virus infectionHuman papillomavirus 16Immunocompromised HostImmunologic Deficiency SyndromesImmunosuppressionIncidenceIndividualInfectionKaposi SarcomaLaboratoriesLeadLeukoplakiaLongevityMalignant - descriptorMalignant ConversionMalignant NeoplasmsMediatingNeoplasmsNude MiceOncogenicOncogenic VirusesOralOral UlcerOral candidiasisOral cavityPathogenesisPatientsPhasePhenotypePilot ProjectsPlayPrevalencePropertyProteinsRBL2 geneRefractoryRetroviral VectorRoleSalivary Gland DiseasesScreening procedureStimulusTP53 geneTestingTrans-ActivatorsTransgenic MiceTumor Suppressor ProteinsTumorigenicityViral OncogeneVirus Replicationcarcinogenesiscell transformationcervical and anal cancerhuman CREB1 proteinkeratinocytemalignant mouth neoplasmmammalian genomemouth squamous cell carcinomanoveloral lesionoral tissueoral wartrepairedresponsesenescencetat Proteintumortumorigenesistumorigenicviral DNAvirus related cancer
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): There is emerging evidence to suggest the direct oncogenic potential of human immunodeficiency virus (HIV) through its trans-activator (Tat) protein. Tat targets the "gate keepers" of mammalian genome, i.e., p53and RB2/p130 tumor suppressors, and may challenge genetic stability by impairing DMA repair activities. Tat may also mediate the interactions of HIV with other oncogenic viruses, such as human papilloma virus (HPV).Tat is released from HIV-infected cells and is capable of penetrating into the target cells, including those harboring HPV DMA. Frequent infection with HPV in the oral cavity has been noted in immunocompromised children and adults infected with HIV. HIV+ patients are more susceptible to infection with multiple HPV subtypes, including types 16 and 18. These "high risk" HPVs are closely associated with development of malignant oral cancer. However, HPV infection alone is not sufficient for tumorigenic cell transformation, which requires additional oncogenic stimuli. Importantly, Tat positively regulates the HPV long control region (LCR) to elevate the expression of E6 and E7 viral oncogenes. Therefore, HIV may enhance the tumorigenic potential of HPV, possibly through Tat.
Our long-range goal is to elucidate the role of HIV Tat in the malignant conversion of human oral keratinocytes harboring "high risk" HPV genome.
The central hypothesis of this project is that HIV Tat enhances the tumorigenicity of HPV in HOKs. We will test this hypothesis through the following Specific Aims: (1) to investigate the effects of HIV Tat on phenotypic alteration, i.e., proliferation, differentiation, senescence, and apoptosis, of NHOK and HOK harboring HPV genome, (2) to determine the effects of HIV Tat on immortalization and tumorigenic potential of NHOK and HOK harboring HPV genome, (3) to identify the cellular genes and proteins differentially expressed by HIV Tat transduction in NHOK and HOK harboring HPV genome. These studies will ultimately lead us to develop a novel mode for early diagnosis and treatment of HPV-related oral lesions in HIV+ patients.
There is emerging evidence to suggest that Tat protein, one of gene products from human immunodeficiency virus (HIV), plays important role in the development of cancer in HIV+ patients. In this study, we will examine the role of Tat protein in the development of cancers, particularly human papilloma virus (HPV)-related cancer in oral tissue.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Epigenetic Control of HPV-associated Oral Carcinogenesis
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批准号:8735930
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项目类别:
-
资助金额:$45.34万
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财政年份:2013
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负责人:Reuben Han-Kyu Kim
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依托单位:
Epigenetic Control of HPV-associated Oral Carcinogenesis
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批准号:9115125
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项目类别:
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资助金额:$45.34万
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财政年份:2013
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负责人:Reuben Han-Kyu Kim
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依托单位:
Molecular mechanisms of drug-induced ONJ and osteomucosal chronic wounds
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批准号:9063982
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项目类别:
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资助金额:$38.5万
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财政年份:2013
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负责人:Reuben Han-Kyu Kim
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依托单位:
Molecular mechanisms of drug-induced ONJ and osteomucosal chronic wounds
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批准号:8734376
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项目类别:
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资助金额:$38.5万
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财政年份:2013
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负责人:Reuben Han-Kyu Kim
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依托单位:
Molecular mechanisms of drug-induced ONJ and osteomucosal chronic wounds
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批准号:8847574
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项目类别:
-
资助金额:$38.5万
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财政年份:2013
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负责人:Reuben Han-Kyu Kim
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依托单位:
Epigenetic Control of HPV-associated Oral Carcinogenesis
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批准号:8622014
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项目类别:
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资助金额:$45.34万
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财政年份:2013
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负责人:Reuben Han-Kyu Kim
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依托单位:
Molecular mechanisms of drug-induced ONJ and osteomucosal chronic wounds
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批准号:8482384
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项目类别:
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资助金额:$38.5万
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财政年份:2013
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负责人:Reuben Han-Kyu Kim
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依托单位:
Role of oral mucosa in bisphosphonate related osteonecrosis of the jaw
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批准号:7977957
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项目类别:
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资助金额:$11.55万
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财政年份:2010
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负责人:Reuben Han-Kyu Kim
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依托单位:
Role of oral mucosa in bisphosphonate related osteonecrosis of the jaw
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批准号:8097435
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项目类别:
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资助金额:$11.55万
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财政年份:2010
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负责人:Reuben Han-Kyu Kim
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依托单位:
Combined Effect on HIV and HPV in Oral Cancer
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批准号:7664921
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项目类别:
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资助金额:$11.46万
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财政年份:2007
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负责人:Reuben Han-Kyu Kim
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依托单位:
Combined Effect on HIV and HPV in Oral Cancer
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批准号:7487830
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项目类别:
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资助金额:$11.04万
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财政年份:2007
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负责人:Reuben Han-Kyu Kim
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依托单位:
Combined Effect on HIV and HPV in Oral Cancer
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批准号:8106228
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项目类别:
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资助金额:$12.16万
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财政年份:2007
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负责人:Reuben Han-Kyu Kim
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依托单位:
Combined Effect on HIV and HPV in Oral Cancer
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批准号:7317543
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项目类别:
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资助金额:$10.68万
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财政年份:2007
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负责人:Reuben Han-Kyu Kim
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依托单位:
海外基金