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HPV and Cervical Cancer: Mechanisms

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Information about HPV and Cervical Cancer: Mechanisms

Published on April 28, 2008

Author: brandolina1

Source: slideshare.net

Description

HPV and Cervical Cancer: a look at some of the signal transduction pathways, mechanisms of carcinogenesis, and therapeutics.
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HPV & Cervical Cancer: Mechanisms Brandy Wells Advanced Cell Biology II Spring 2008, Johns Hopkins University

Cervical Cancer Basics Cancer of the cervix 2 nd most common cancer in women worldwide Profiles like an STD (sexually transmitted disease) because of STD-dependent development

Cancer of the cervix

2 nd most common cancer in women worldwide

Profiles like an STD (sexually transmitted disease) because of STD-dependent development

HPV is Necessary Cause of Cervical Cancer Human papillomavirus DNA required for development of cervical cancer HPV DNA detected in 90-100% of cervical cancer specimens compared to 5-20% in epidemiological control specimens Bosch et al., 2002.

Human papillomavirus DNA required for development of cervical cancer

HPV DNA detected in 90-100% of cervical cancer specimens compared to 5-20% in epidemiological control specimens

HPV is Epitheliotropic All characterized strains only infect epithelial cells, specifically skin anogenital mucosa oropharyngeal mucosa Human Papillomavirus model*

All characterized strains only infect epithelial cells, specifically

skin

anogenital mucosa

oropharyngeal mucosa

HPV Genome E1-E7 = “Early” genes (nonstructural) L1, L2 = Capsid genes URR = upstream regulatory region E6 & E7 proteins play major role in immortality & malignant transformation of infected cells E5 has role, but not required to maintain cancer phenotype Munoz et al. 2006.

E1-E7 = “Early” genes (nonstructural)

L1, L2 = Capsid genes

URR = upstream regulatory region

E6 & E7 proteins play major role in immortality & malignant transformation of infected cells

E5 has role, but not required to maintain cancer phenotype

HPV Classification: Carcinogenic Risk Over 100 HPV strains identified Risk assessment based on transformative potential of a strain’s E proteins Low  found in benign lesions only Intermediate  found in benign lesions & invasive cancers High  usually found in carcinomas; occasionally seen in benign lesions Furumoto et al., 2002. 16, 18, 45, 56 High Risk 31, 33, 35, 51, 52, 58 Intermediate Risk 60, 11, 42, 43, 44 Low Risk

Over 100 HPV strains identified

Risk assessment based on transformative potential of a strain’s E proteins

Low  found in benign lesions only

Intermediate  found in benign lesions & invasive cancers

High  usually found in carcinomas; occasionally seen in benign lesions

Early Genes Hijack Cell Cycle Checkpoint HPV’s E6 & E7 proteins interact with key cell cycle proteins including pRB & p53, effectively over-riding the G 1 /S-phase checkpoint Mechanism E7 binds & phosphorylates pRB, activating E2F transcription factor DNA replication proteins of host cell are then expressed; unchecked S-phase occurs E6 marks p53 for proteolytic degradation so it cannot activate apoptosis ( note: absence of p53 is not necessary for E6 to cause immortalization)

HPV’s E6 & E7 proteins interact with key cell cycle proteins including pRB & p53, effectively over-riding the G 1 /S-phase checkpoint

Mechanism

E7 binds & phosphorylates pRB, activating E2F transcription factor

DNA replication proteins of host cell are then expressed; unchecked S-phase occurs

E6 marks p53 for proteolytic degradation so it cannot activate apoptosis ( note: absence of p53 is not necessary for E6 to cause immortalization)

E6 & E7 in Cervical Cancer Progression Furumoto et al., 2002.

Consequences of the HPV Hijack Keratinocyte differentiation retarded Checkpoint dependence gone Chromosomal instability; accumulation of oncogenic mutations Increased loss of cell cycle/growth control Cancer

Keratinocyte differentiation retarded

Checkpoint dependence gone

Chromosomal instability; accumulation of oncogenic mutations

Increased loss of cell cycle/growth control

Cancer

High-Risk HPV Oncoproteins: E6 Hausen, 2000. (1) Band et al., 1990 (2) Werness et al., 1990 & Sheffner et al., 1993 (3) Werness et al., 1990 & Thomas, 1998 (4) White et al.,1994 (5) Kessis et al., 1996 & Havre et al., 1995 (6) Klingelhutz et al., 1996 (7) Ronco et al., 1998 (8) Banks et al., 1998 & 1999 (1) Cell immmortalization (2) Binding of E6-associated protein results in degradation of specific host cell proteins [p53] (3) Anti-apoptotic effect (4) Chromosomal destabilization (5) Enhancement of foreign DNA integration & mutagenicity (6) Activation of telomerase (7) Blockade of interferon functions (8) Degradation of Bak protein Investigator E6 Identified Function

E6 is Pleiotropic Stimulates expression of transcription factor HIF-1 α Prognostic Marker: Higher levels of HIF-1 α expression in early-stage invasive cervical cancer correlated to shorter overall survival time HPV-16 E6 protein from SWISS-Model Repository (P03126)

Stimulates expression of transcription factor HIF-1 α

Prognostic Marker: Higher levels of HIF-1 α expression in early-stage invasive cervical cancer correlated to shorter overall survival time

Significance of HIF-1 α Expression in Cervical Cancer In cells with normal functioning p53 , HIF-1 α is expressed in instances of hypoxia (as its name, hypoxia-inducible factor , implies) HIF-1 α binds & stabilizes p53 to induce apoptosis of hypoxic cells, however p53 is degraded by E6 in HPV-infected cells Instead, HIF-1 α stimulates neoangiogenesis for tumor cells, providing the vascularization necessary for cancer progression

In cells with normal functioning p53 , HIF-1 α is expressed in instances of hypoxia (as its name, hypoxia-inducible factor , implies)

HIF-1 α binds & stabilizes p53 to induce apoptosis of hypoxic cells, however p53 is degraded by E6 in HPV-infected cells

Instead, HIF-1 α stimulates neoangiogenesis for tumor cells, providing the vascularization necessary for cancer progression

Evidence of HIF-1 α Overexpression in Cervical Cancer No expression of HIF-1 α in normal specimens Antibody treatment less likely to disrupt normal cells HIF-1 α expression identified by nuclear staining/ immunohistochemistry A B Invasive cervical cancer specimens exhibiting strong (A) & weak (B) HIF-1 α expression Birner et al., 2000

No expression of HIF-1 α in normal specimens

Antibody treatment less likely to disrupt normal cells

HIF-1 α expression identified by nuclear staining/ immunohistochemistry

Candidate for Anti-angiogenesis Therapy? Reduction of HIF-1 α -induced angiogenesis may slow progression rate by cutting off oxygen & nutrient supply to tumor cells HIF-1 α mediates angiogenesis through activation of VEGF pathway Vascular endothelial growth factor stimulates angiogenesis & release of similar factors AntiHIF-1 α or antiVEGF antibody treatment may control progression of cervical cancer

Reduction of HIF-1 α -induced angiogenesis may slow progression rate by cutting off oxygen & nutrient supply to tumor cells

HIF-1 α mediates angiogenesis through activation of VEGF pathway

Vascular endothelial growth factor stimulates angiogenesis & release of similar factors

AntiHIF-1 α or antiVEGF antibody treatment may control progression of cervical cancer

High-Risk HPV Oncoproteins: E7 Hausen, 2000. (1) Munger & Phelps, 1993 (2) Arroyo et al., 1993 & Zerfass et al., 1995 (3) Putthenveettil et al., 1996 (4) Jones et al., 1997 & Funk et al., 1997 (5) Kessis et al., 1996 & Reznikoff et al., 1996 (6) Oda et al., 1999 (7) Dyson et al., 1989, 1992. (1) Cell immmortalization (2) Activation of cyclins E & A (3) Induction of apoptosis (4) Inhibition of cyclin-dependent kinase inhibitors (5) Enhancement of foreign DNA integration & mutagenicity (6) Degradation of Blk tyrosine kinase (7) Inactivation of retinoblastoma protein-related pocket proteins Investigator E7 Identified Function

E7 is Pleiotropic Inactivation of p21 CIP-1 & p27 KIP-1 (cdk inhibitors) results in growth stimulation of infected cells Inactivation of tumor suppressor transcription factor interferon 1 ( IRF-1 ) through direct interaction HPV-1a E7 protein from SWISS-Model Repository (P06465)

Inactivation of p21 CIP-1 & p27 KIP-1 (cdk inhibitors) results in growth stimulation of infected cells

Inactivation of tumor suppressor transcription factor interferon 1 ( IRF-1 ) through direct interaction

IRF-1 Deactivation by E7 May explain the immune-resistance mechanism of HPV-infected cervical cancer cells 1. IRF-1 activated during exposure to viral infection, IFNs, TNF α , etc. 2. Histone deacetylase ( HDAC ) mediates accessibility to chromatin of IRF-1 inducible genes, such as IFN- β 3. IFN- β expression stimulates anti-proliferative effect on cell Normal role of IRF-1 in tumor suppressor mechanism

May explain the immune-resistance mechanism of HPV-infected cervical cancer cells

1. IRF-1 activated during exposure to viral infection, IFNs, TNF α , etc.

2. Histone deacetylase ( HDAC ) mediates accessibility to chromatin of IRF-1 inducible genes, such as IFN- β

3. IFN- β expression stimulates anti-proliferative effect on cell

Mechanism of IRF-1 Inactivation E7 interacts with HDAC and IRF-1 Blocks expression of IRF-1 inducible genes by inhibiting HDAC Result: Cell proliferation evades immune response Park et al., 2000.

E7 interacts with HDAC and IRF-1

Blocks expression of IRF-1 inducible genes by inhibiting HDAC

Result: Cell proliferation evades immune response

Notch1 Signaling Pathway in HPV-Cervical Cancer Notch1 expression would inhibit expression of HPV regulatory region (URR ) & subsequent E6 / E7 expression Novel protective role against HPV-induced transformation Talora et al., 2002.

Notch1 expression would inhibit expression of HPV regulatory region (URR ) & subsequent E6 / E7 expression

Novel protective role against HPV-induced transformation

Consequences of Notch1 Downregulation Downregulation of Notch1 expression inhibits cell growth & differentiation Required for maintenance of malignant phenotype in later stages of invasive cervical cancer (maintains E6/E7 expression) Mechanism poorly understood, but may eventually reveal drug target A/B: Notch1 staining in normal cervical biopsy Notch1 staining in CIN lesion (C) & invasive cervical cancer (D) biopsies Talora et al., 2002.

Downregulation of Notch1 expression inhibits cell growth & differentiation

Required for maintenance of malignant phenotype in later stages of invasive cervical cancer (maintains E6/E7 expression)

Mechanism poorly understood, but may eventually reveal drug target

E6 & E7 Integrate into Host Genome Progression of the tumor condition requires integration of viral genes into host genome Chromatin remodeling or negative regulation of transcription (involving E2) Benign or pre-malignant lesions show viral genes to be extrachromosomal Consequences Stabilization of mRNA transcripts of viral genes Results in constant E6 & E7 levels required to maintain phenotype of malignant cells

Progression of the tumor condition requires integration of viral genes into host genome

Chromatin remodeling or negative regulation of transcription (involving E2)

Benign or pre-malignant lesions show viral genes to be extrachromosomal

Consequences

Stabilization of mRNA transcripts of viral genes

Results in constant E6 & E7 levels required to maintain phenotype of malignant cells

Carcinogenesis by HPV Bosch et al. 2002.

Preventative Intervention Vaccination against HPV infection HPV testing (PCR) is useful as an alternative primary screening tool for cervical cancer Clinical trials have indicated HPV testing as a way to solve cases where cytology-based screening results are ambiguous Determination of strain (e.g. HPV-16) characterizes associated carcinogenic risk

Vaccination against HPV infection

HPV testing (PCR) is useful as an alternative primary screening tool for cervical cancer

Clinical trials have indicated HPV testing as a way to solve cases where cytology-based screening results are ambiguous

Determination of strain (e.g. HPV-16) characterizes associated carcinogenic risk

CIN: Pre-Cancerous Warning Cervical intraepithelial neoplasia (CIN) observed in disease progression New, abnormal, disorganized growth of cervix epithelium Gynecological CIN Diagnosis Atypical Pap smear (not definitive!) Culposcopy: definitively determines if CIN present by examining specimen under culposcope

Cervical intraepithelial neoplasia (CIN) observed in disease progression

New, abnormal, disorganized growth of cervix epithelium

Gynecological CIN Diagnosis

Atypical Pap smear (not definitive!)

Culposcopy: definitively determines if CIN present by examining specimen under culposcope

Stages of CIN 1. CIN I Number & depth of abnormal cells is low 2. CIN II Abnormal cell growth penetrates about ½ the thickness of cervical epithelium 3. CIN III “ carcinoma in-situ” Abnormal cell growth penetrates entire thickness of cervical epithelium 4. Invasive Cervical Cancer Abnormal cell growth penetrates beyond cervical epithelium

1. CIN I

Number & depth of abnormal cells is low

2. CIN II

Abnormal cell growth penetrates about ½ the thickness of cervical epithelium

3. CIN III

“ carcinoma in-situ”

Abnormal cell growth penetrates entire thickness of cervical epithelium

4. Invasive Cervical Cancer

Abnormal cell growth penetrates beyond cervical epithelium

Stages of CIN: Histology NORMAL CIN I CIN II CIN III Furumoto et al., 2002.

Cervical Cancer Cofactors HPV is NOT sufficient cause for cervical cancer Combination of HPV & 1 or more cofactors increase risk of cancer progression Hormonal contraceptives Smoking Parity

HPV is NOT sufficient cause for cervical cancer

Combination of HPV & 1 or more cofactors increase risk of cancer progression

Hormonal contraceptives

Smoking

Parity

HPV Vaccination Gardasil ® is only FDA-approved viral vaccine for HPV 16*, 18*, 6 & 11 *high risk strains Contains purified virus-like particles (VLPs) of L1 gene product to activate humoral immune response in host L1 = major capsid (structural) protein VLPs = self-assembled capsid proteins in immuno-relevant organization

Gardasil ® is only FDA-approved viral vaccine for HPV 16*, 18*, 6 & 11

*high risk strains

Contains purified virus-like particles (VLPs) of L1 gene product to activate humoral immune response in host

L1 = major capsid (structural) protein

VLPs = self-assembled capsid proteins in immuno-relevant organization

Treatment Options Cryotherapy/laser surgery – freezing off or cutting away of abnormal cervical epithelial cells Partial/full hysterectomy – removal of uterus & cervix, sometimes ovaries & fallopian tubes Radiation therapy/chemotherapy

Cryotherapy/laser surgery – freezing off or cutting away of abnormal cervical epithelial cells

Partial/full hysterectomy – removal of uterus & cervix, sometimes ovaries & fallopian tubes

Radiation therapy/chemotherapy

References Bosch et al. 2002. The causal relationship between human papillomavirus and cervical cancer. J Clin Pathol 55:244-265. Birner et al. 2000. Overexpression of Hypoxia-inducible Factor 1 α Is a Marker for Unfavorable Prognosis in Early-stage Invasive Cervical Cancer. Cancer Research 60:4693-4696 Furumoto et al. 2002. Human papillomavirus (HPV) and cervical cancer. J Medical Investigation 49:124-122. Hausen, H. 2000. Papillomaviruses Causing Cancer: Evasion from Host-Cell Control in Early Events in Carcinogenesis. J Natl Cancer Inst 92:690–8 Munoz et al. 2006. HPV in the etiology of human cancer. Vaccine 24S3:S3/1-S3/10 Park et al. 2000. Inactivation of Interferon Regulatory Factor-1 Tumor Suppressor Protein by HPV E7 Oncoprotein. J Bio Chem 275;10:6764-6769. Talora et al. 2002. Specific down-modulation of Notch1 signaling in cervical cancer cells is required for sustained HPV-E6/E7 expression and late steps of malignant transformation. Genes & Dev 16:2252-2263 http://emc.medicines.org.uk/emc/assets/c/html/DisplayDoc.asp?DocumentID=19016

Bosch et al. 2002. The causal relationship between human papillomavirus and cervical cancer. J Clin Pathol 55:244-265.

Birner et al. 2000. Overexpression of Hypoxia-inducible Factor 1 α Is a Marker for Unfavorable Prognosis in Early-stage Invasive Cervical Cancer. Cancer Research 60:4693-4696

Furumoto et al. 2002. Human papillomavirus (HPV) and cervical cancer. J Medical Investigation 49:124-122.

Hausen, H. 2000. Papillomaviruses Causing Cancer: Evasion from Host-Cell Control in Early Events in Carcinogenesis. J Natl Cancer Inst 92:690–8

Munoz et al. 2006. HPV in the etiology of human cancer. Vaccine 24S3:S3/1-S3/10

Park et al. 2000. Inactivation of Interferon Regulatory Factor-1 Tumor Suppressor Protein by HPV E7 Oncoprotein. J Bio Chem 275;10:6764-6769.

Talora et al. 2002. Specific down-modulation of Notch1 signaling in cervical cancer cells is required for sustained HPV-E6/E7 expression and late steps of malignant transformation. Genes & Dev 16:2252-2263

http://emc.medicines.org.uk/emc/assets/c/html/DisplayDoc.asp?DocumentID=19016

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