Microbial and epigenetic factors in the pathogenesis of nasopharyngeal carcinoma
Author: Zhou, Xiaoying
Date: 2015-11-10
Location: Hillarp lecture hall, Retzius väg 8, Karolinska Institutet, Solna
Time: 13.00
Department: Inst för mikrobiologi, tumör- och cellbiologi / Dept of Microbiology, Tumor and Cell Biology
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Thesis (874.0Kb)
Abstract
While uncommon in most of the world, nasopharyngeal carcinoma (NPC) shows an unusual geographic and ethnic distribution, being highly prevalent in Southern China and Southeast Asia. Genetic susceptibility, Epstein-Barr virus (EBV) infection and additional environmental exposures are well established risk factors for NPC in endemic areas. However, the detailed molecular mechanisms of NPC pathogenesis remain largely unknown. In this thesis, several novel pathogenic mechanisms of NPC development and progression are presented.
The interaction of EBV encoded latent membrane protein 2A (LMP2A) with cellular proteins promoting invasiveness of NPC cells is described in paper I. Spleen tyrosine kinase (Syk) interacts with integrin β4 subunit (ITGβ4) in epithelial cells through an ITAM-like motif, and concurrent LMP2A expression interferes with this interaction by competitive binding to Syk. Both Syk and LMP2A affect cell surface expression of ITGβ4. Particularly, ITGβ4 concentrates at cellular protrusions in LMP2A expressing cells, which may contribute to the migration property of NPC-cells.
Paper II and paper III focus on the epigenetic alteration of candidate tumor suppressor genes (TSGs) and their possible role in NPC tumorigenesis. Cadherin 4 (CDH4) and ubiquitin-conjugating enzyme 2L6 (UBE2L6) are downregulated due to promoter hypermehtylation in NPC. Both genes suppress the proliferation and colony formation of NPC-cells. CDH4 impedes cell migration and elicits cell communication; UBE2L6 induce apoptosis of NPC cells and counteracts degradation of adipocyte triglyceride lipase (ATGL) through ISG15-conjugation of valosin-containing protein (VCP). CDH4 and UBE2L6 could be involved in both initiation and progression of NPC. Suppression of UBE2L6 encoded protein UbcH8 correlated with poor outcome in NPC patients.
In paper IV, we compared the response of NPC and normal nasopharyngeal epithelial (NNE) cell lines to bacteria and bacterial cell wall components. Strong nuclear translocation of NF-κB and significant induction of proinflammatory factors IL6, IL8, IL1α and CXCL2 were observed in NNE cells, but not in NPC cells upon exposure to Gram-positive bacteria streptococci and peptidoglycan (PGN). We identified three different mechanisms by which the activation of NF-κB in NPC cells could be hampered. It could be trapped by an enhanced accumulation of cytoplasmic lipids. I-κB degradation could be impaired due to downregulation of UBE2L6. We also showed that overexpression of lysine-specific demethylase-1 (LSD1) blocked the transcriptional activation of proinflammatory genes. Together these mechanisms might contribute to decreased immune reactivity in NPC and thus affect tumor progression.
The interaction of EBV encoded latent membrane protein 2A (LMP2A) with cellular proteins promoting invasiveness of NPC cells is described in paper I. Spleen tyrosine kinase (Syk) interacts with integrin β4 subunit (ITGβ4) in epithelial cells through an ITAM-like motif, and concurrent LMP2A expression interferes with this interaction by competitive binding to Syk. Both Syk and LMP2A affect cell surface expression of ITGβ4. Particularly, ITGβ4 concentrates at cellular protrusions in LMP2A expressing cells, which may contribute to the migration property of NPC-cells.
Paper II and paper III focus on the epigenetic alteration of candidate tumor suppressor genes (TSGs) and their possible role in NPC tumorigenesis. Cadherin 4 (CDH4) and ubiquitin-conjugating enzyme 2L6 (UBE2L6) are downregulated due to promoter hypermehtylation in NPC. Both genes suppress the proliferation and colony formation of NPC-cells. CDH4 impedes cell migration and elicits cell communication; UBE2L6 induce apoptosis of NPC cells and counteracts degradation of adipocyte triglyceride lipase (ATGL) through ISG15-conjugation of valosin-containing protein (VCP). CDH4 and UBE2L6 could be involved in both initiation and progression of NPC. Suppression of UBE2L6 encoded protein UbcH8 correlated with poor outcome in NPC patients.
In paper IV, we compared the response of NPC and normal nasopharyngeal epithelial (NNE) cell lines to bacteria and bacterial cell wall components. Strong nuclear translocation of NF-κB and significant induction of proinflammatory factors IL6, IL8, IL1α and CXCL2 were observed in NNE cells, but not in NPC cells upon exposure to Gram-positive bacteria streptococci and peptidoglycan (PGN). We identified three different mechanisms by which the activation of NF-κB in NPC cells could be hampered. It could be trapped by an enhanced accumulation of cytoplasmic lipids. I-κB degradation could be impaired due to downregulation of UBE2L6. We also showed that overexpression of lysine-specific demethylase-1 (LSD1) blocked the transcriptional activation of proinflammatory genes. Together these mechanisms might contribute to decreased immune reactivity in NPC and thus affect tumor progression.
List of papers:
I. Xiao-Ying Zhou, Liudmila Matskova, Li-Sophie Z. Rathje, Xue Xiao, Gerald Gish, Maria Werner, Ilya Ignatyev, Na-Na Yu, Wei-Lin Zhao, Fang-Yun Tian, Bo Hou, Zhe Zhang, Tony Pawson, Fu Chen, Ingemar Ernberg. SYK interaction with ITGβ4 suppressed by Epstein-Barr Virus LMP2A modulates migration and invasion of Nasopharyngeal Carcinoma Cells. Oncogene. 2015 Aug 20;34(34):4491-4499.
Fulltext (DOI)
Pubmed
II. Chun-Ping Du, Ting-Ting Huang, Di Sun, Ying-Xi Mo, Hai-Yan Feng, Xiao-Ying Zhou, Xue Xiao, Na-Na Yu, Bo Hou, Guang-Wu Huang, Ingemar Ernberg, Zhe Zhang. CDH4 as a novel putative tumor suppressor gene epigenetically silenced by promoter hypermethylation in nasopharyngeal carcinoma. Cancer Lett. 2011 Oct 1; 309 (1):54-61.
Fulltext (DOI)
Pubmed
View record in Web of Science®
III. Xiao-Ying Zhou, Jia-Zhang Wei, Fu Chen, Xue Xiao, Ting-Ting Huang, Qian He, Shu-Min Wang, Chun-Ping Du, Ying-Xi Mo, Long-De Lin, Ying Xie, Li-Li Wei, Ying Lan, Mairiko Murata, Guang-Wu Huang, Ingemar Ernberg, Liudmila Matskova, Zhe Zhang. Epigenetic downregulation of the ISG15-conjugating enzyme UbcH8 impairs lipolysis and correlates with poor prognosis in nasopharyngeal carcinoma. [Accepted]
Fulltext (DOI)
Pubmed
View record in Web of Science®
IV. Xiao-Ying Zhou, Liudmila Matskova, Xue Xiao, Yu-Feng Chen, Feng He, Guang-Wu Huang, Zhe Zhang, Ingemar Ernberg. Induction of inflammatory response in nasopharyngeal epithelial cells by microflora components is impaired in nasopharyngeal carcinoma cells. [Manuscript]
I. Xiao-Ying Zhou, Liudmila Matskova, Li-Sophie Z. Rathje, Xue Xiao, Gerald Gish, Maria Werner, Ilya Ignatyev, Na-Na Yu, Wei-Lin Zhao, Fang-Yun Tian, Bo Hou, Zhe Zhang, Tony Pawson, Fu Chen, Ingemar Ernberg. SYK interaction with ITGβ4 suppressed by Epstein-Barr Virus LMP2A modulates migration and invasion of Nasopharyngeal Carcinoma Cells. Oncogene. 2015 Aug 20;34(34):4491-4499.
Fulltext (DOI)
Pubmed
II. Chun-Ping Du, Ting-Ting Huang, Di Sun, Ying-Xi Mo, Hai-Yan Feng, Xiao-Ying Zhou, Xue Xiao, Na-Na Yu, Bo Hou, Guang-Wu Huang, Ingemar Ernberg, Zhe Zhang. CDH4 as a novel putative tumor suppressor gene epigenetically silenced by promoter hypermethylation in nasopharyngeal carcinoma. Cancer Lett. 2011 Oct 1; 309 (1):54-61.
Fulltext (DOI)
Pubmed
View record in Web of Science®
III. Xiao-Ying Zhou, Jia-Zhang Wei, Fu Chen, Xue Xiao, Ting-Ting Huang, Qian He, Shu-Min Wang, Chun-Ping Du, Ying-Xi Mo, Long-De Lin, Ying Xie, Li-Li Wei, Ying Lan, Mairiko Murata, Guang-Wu Huang, Ingemar Ernberg, Liudmila Matskova, Zhe Zhang. Epigenetic downregulation of the ISG15-conjugating enzyme UbcH8 impairs lipolysis and correlates with poor prognosis in nasopharyngeal carcinoma. [Accepted]
Fulltext (DOI)
Pubmed
View record in Web of Science®
IV. Xiao-Ying Zhou, Liudmila Matskova, Xue Xiao, Yu-Feng Chen, Feng He, Guang-Wu Huang, Zhe Zhang, Ingemar Ernberg. Induction of inflammatory response in nasopharyngeal epithelial cells by microflora components is impaired in nasopharyngeal carcinoma cells. [Manuscript]
Institution: Karolinska Institutet
Supervisor: Ingemar, Ernberg
Issue date: 2015-10-19
Rights:
Publication year: 2015
ISBN: 978-91-7676-125-0
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