chapter 3 tumor viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 mar 15, 2007

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Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

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Page 1: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Chapter 3

Tumor Viruses

3.1, 3.2, 3.5

3.7 - 3.11

3.4

Mar 15, 2007

Page 2: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

What is a virus ? - A virus is a microscopic particle (ranging in size from 20 - 300 nm) that can infect the cells of a biological organism. Viruses can replicate themselves only by infecting a host cell and, therefore, cannot reproduce on their own.

Virion: virus particle including a capsid (coat) and the viral genome

Page 3: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Figure 3.1 The Biology of Cancer (© Garland Science 2007)

3.1 Peyton Rous discovered a chicken sarcoma virus (1909)

Page 4: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Peyton Rous

1. Discovered a virus that causes

cancers in chickens (Rous

sarcoma virus, 1911)

2. His findings:

(1) established a precedent

that some viruses can

cause cancers

(2) cancer viruses provide a

genetic simplification for the

study of cancer

Page 5: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Figure 3.4a The Biology of Cancer (© Garland Science 2007)

3.2 Rous sarcoma virus is discovered to transform infected cells in culture

A focus of Rous sarcoma virus (RSV) -transformed chicken embryo fibroblasts surrounded by a monolayer of uninfected cells.

Page 6: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Transformation

- Process of converting a normal cell into a cell having some or many of the attributes of a cancer cell

Page 7: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Table 3.2 The Biology of Cancer (© Garland Science 2007)

3.5 Tumor viruses induce multiple changes in cell phenotype including acquisition of tumorigenicity

1.2.3.4.5.6.

7.8.9.

Page 8: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

1.Altered morphology – rounded, refractile

Page 9: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

2. Loss of contact inhibition - ability to grow over one another (pile up)

6. High saturation density - ability to accumulate large numbers of cells in culture dish

Page 10: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Figure 3.12 The Biology of Cancer (© Garland Science 2007)

Anchorage-independent growth

3. Ability to grow without attachment to solid substrate - anchorage independence

Page 11: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

4. Ability to proliferate indefinitely - immortalization (Chapter 10)

5. Reduced requirement for mitogenic growth factors

7. Inability to halt proliferation in response to deprivation of growth factors

8. Increased transport of glucose

Page 12: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Figure 3.13 The Biology of Cancer (© Garland Science 2007)

9. tumorigencity

Immunocomprimizednude mice

- no thymus (no T cell response)

- no hair

Page 13: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Figure 3.17 The Biology of Cancer (© Garland Science 2007)

3.7 Retroviral genomes become integrated into the chromosomes of infected cells

- Tumor viruses consist of DNA tumor viruses and RNA tumor viruses

- Rous sarcoma virus (RSV) is an RNA virus. How could the genomic RNA integrate into the chromosomal DNA of an infected cell?

Page 14: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

The virion of RSV (and other related viruses)

Page 15: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

The life cycle of an RNA tumor virus (e.g., RSV)

Retrovirus

(RT)

Page 16: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Howard Temin

David Baltimore

Renato Dulbecco

1. Propose provirus hypothesis

for retroviruses

2. Purification of reverse transcriptase

3. Focus assays

1. Purification of reverse transcriptase

2. Virion polymerases

1. Study on oncogenic DNA tumor

virus

2. Interaction between polyoma virus

(and SV40) with host cells

Page 17: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Figure 3.19 The Biology of Cancer (© Garland Science 2007)

3 retroviral genes for viral replication.

Which one is responsible for transformation?

The genome of retroviruses

Page 18: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Structure of the Rous sarcoma virus genome

avian leukosis virus → - very slowly transforming

Rous sarcoma virus → - rapidly transforming

sarcoma

Page 19: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Figure 3.20 (part 2 of 2) The Biology of Cancer (© Garland Science 2007)

genomic DNA from normal chicken cells

3.8 A version of the src gene carried by RSV is also present in uninfected cells

Page 20: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Figure 3.21 The Biology of Cancer (© Garland Science 2007)

Evolutionary tree of the src gene

The presence of src sequences was later found in Drosophila and even a sponge.

Page 21: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Figure 3.22 The Biology of Cancer (© Garland Science 2007)

3.9 RSV exploits a kidnapped cellular gene to transform cells

srcv-src : an oncogenec-src : a proto-oncogene

Page 22: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Harold Varmus

Michael Bishop

1. Cellular origin of retroviral

oncogenes

2. Retroviral transduction

3. Roles of proto-oncogenes

Page 23: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Extended ideas from these findings:

1. If retroviruses could activate c-src proto-oncogene into a potent oncogene, perhaps other carcinogens might operate in a similar way.

2. All of the transforming powers of RSV derived from the presence of a single gene – v-src. Thus, a single oncogene can change the shape, metabolism, and growth behavior of a cell.

3. Other retroviruses may acquire oncogenes from other proto-oncogenes.

Page 24: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

3.10 The vertebrate genome carries a large group of proto-oncogenes

Table 3.3 The Biology of Cancer (© Garland Science 2007)

Page 25: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Figure 3.23a The Biology of Cancer (© Garland Science 2007)

3.11 Slowly transforming retroviruses activate proto-oncogenes by inserting their genomes adjacent to these cellular genes

Can RNA viruses which do not carry oncogenes cause cancers?

Page 26: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Figure 3.23b The Biology of Cancer (© Garland Science 2007)

transcription of myc gene is controlled by viral promoters

excessive myc protein

Insertional mutagenesis

Page 27: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Table 3.4 The Biology of Cancer (© Garland Science 2007)

Page 28: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Table 3.1 The Biology of Cancer (© Garland Science 2007)

3.4 Viruses containing DNA molecules are also able to induce cancer

Page 29: Chapter 3 Tumor Viruses 3.1, 3.2, 3.5 3.7 - 3.11 3.4 Mar 15, 2007

Life cycle of DNA viruses Integration of SV40 genome

3.6 DNA Tumor virus genomes persist in virus-transformed cells by becoming part of host cell DNA