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Viruses and Cancer

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Viruses and Cancer Cancers of viral aetiology Hepatocellular carcinoma (HBV and HCV) Burkitt s lymphoma (EBV) nasopharyngeal carcinoma (EBV) Hodgkins disease (EBV ... – PowerPoint PPT presentation

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Title: Viruses and Cancer


1
Viruses and Cancer
2
Cancers of viral aetiology
  • Hepatocellular carcinoma (HBV and HCV)
  • Burkitts lymphoma (EBV)
  • nasopharyngeal carcinoma (EBV)
  • Hodgkins disease (EBV)
  • cervical carcinoma (HPV)
  • Kaposis sarcoma (HHV-8)
  • adult T cell leukaemia/lymphoma (HTLV-1)

3
Criteria
  • epidemiology
  • virus in tumour tissue
  • viral genes and oncogenesis

4
Mechanisms of Oncogenesis
  1. modulation of cell cycle control (The virus may
    alter the regulatory mechanisms controlling the
    progress of the cell cycle and cell division)
  2. modulation of apoptosis (the virus must prevent
    the host cell from undergoing apoptosis, a normal
    cellular response to viral-induced injury, which
    would otherwise abort the further development of
    uncontrolled cell proliferation)
  3. ROS (Reactive oxygen species) mediated damage

5
Cell Cycle Control
  • pRB ( a tumor suppressor protein that is
    dysfunctional in several major cancers. One
    function of pRb is to prevent excessive cell growt
    h by inhibiting cell cycle progression until a
    cell is ready to divide)
  • cyclin D1 (cell cycle control)

6
Modulation of Apoptosis
  • P53 (transcription factor activated by DNA damage
    that can induce growth arrest and apoptosis)
  • Bcl-2 (supress apoptosis)
  • FLICE inhibitory proteins (FLIPs) (inhibit
    apoptosis signalling)

7
ROS Damage
  • inflammatory responses generate radicals,
    including OH. and NO.
  • free radicals target
  • DNA (mutation)
  • protein (nitration, nitrosation)
  • RNA
  • lipids (lipid peroxidation)

8
ROS Damage
  • Free radicals may promote cancer by
  • mutating cancer related genes
  • activating signal transduction pathways
  • promoting angiogenesis
  • exerting selective pressure (p53 and NO.)

9
Hepatocellular Carcinoma
10
Hepatocellular Carcinoma
  • HCC is one of the most prevalent malignant
    diseases in the world
  • chronic infection with HBV or HCV accounts for
    more than 80 of HCC cases
  • other risk factors include aflatoxin B1, heavy
    alcohol consumption and smoking

11
HCC and HBV
  • insertional activation
  • HBx
  • transactivation of proinflammatory genes
  • interaction with p53
  • generation of ROS

12
HCC and HCV
  • HCV sequences are present in HCC tissue
  • HCV antigen expression in HCC (or other tissue)
    cannot be assessed
  • HCV contains genes with potential oncogenic
    function

13
HCV genes
  • HCV core protein has been shown to
  • cause HCC in transgenic mice
  • modulate apoptosis
  • drive cells to proliferation
  • generate ROS

14
HCC and hepatitis viruses
  • mass vaccination against HBV will radically
    reduce the incidence of HCC in SE Asia
  • elimination of HCV or HBV reduces the risk of
    developing HCC

15
Human Herpesvirus 8 and Kaposis Sarcoma
16
Kaposis Sarcoma
  • Kaposis sarcoma (KS) is a mesenchymal tumour
    involving blood and lymphatic vessels
  • KS occurs in three forms
  • classical
  • endemic
  • epidemic

17
Pathology of KS
  • Multicentric lesions composed of interweaving
    bands of spindle cells that form irregular
    vascular channels
  • Spindle cells express markers of endothelial
    cells (CD34 and Factor VIII)

18
KS and HIV
  • The incidence of KS in HIV positive gay men is
    20,000 fold that of the general population
  • KS is 20 times more common in homosexual men with
    AIDS than other risk groups
  • the risk of KS in HIV positive men increases with
    the frequency and risk of sexual activity

19
Herpesviruses and KS
  • In 1994 RDA isolated viral sequences from KS
    tissue
  • these sequences were identified as a new
    herpesvirus, designated HHV-8
  • HHV-8 has now been found in almost 100 of
    tissues from all forms of KS

20
Epidemiology
  • HHV-8 seropositivity in various populations is
    correlated with the population risk of KS
  • Longtitudinal surveys have shown infection with
    HHV-8 precedes the onset of KS

21
Virus and Tumour Tissue
  • In individuals with KS, HHV-8 sequences are found
    in tumour but not in adjacent tissue
  • within KS lesions, HHV-8 DNA and antigen
    expression is localised to spindle cells

22
Genes and oncogenesis
  • HHV-8 encodes homologues of human proteins
  • (examples)
  • cyclin D1
  • G-protein coupled receptor
  • bcl-2
  • FLICE inhibitory protein
  • And others

23
v-cyclin D1
  • HHV-8 v-cyclin is expressed in KS lesions and
    interacts with CDK6
  • v-cyclin in complex with CDK6 is not inhibited by
    p16 INK4a or p27Kip1

24
HHV-8 (G protein-coupled receptor) GPCR
  • HHV-8 encodes a viral G protein-coupled receptor
    (vGPCR).
  • v-GPCR is homologous to the IL-8 receptor
  • v-GPCR has been shown to transform cells and
    tumour formation.

25
HHV-8 bcl-2
  • the viral protein has both sequence and
    structural homology to bcl-2 family proteins
  • v-bcl-2 is functional
  • the role of v-bcl-2 in the viral life cycle is
    not yet clear

26
v-FLIP
  • v-FLIPs inhibit apoptosis signalling through
    death receptors
  • HHV-8 v-FLIP physically interacts with
    pro-caspase-8 and prevents recruitment to DISC

27
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28
Non-homologous Viral Genes
  • Latency -associated nuclear antigen (LANA) is
    essential to the maintenance of HHV-8
  • LANA interacts with p53 and suppresses its
    transcriptional activity
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