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1102273
Herceptin and cancer
Description
Undergraduate BMS238 Cell and molecular biology (Cancer) Mind Map on Herceptin and cancer, created by Kristi Brogden on 29/07/2014.
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bms238 cell and molecular biology
cancer
undergraduate
Mind Map by
Kristi Brogden
, updated more than 1 year ago
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Created by
Kristi Brogden
over 10 years ago
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Resource summary
Herceptin and cancer
Cancer
Can be caused by
Physical carcinogens
Ultraviolet and ionizing radiation
Biological carcinogens
Infections from certain viruses, bacteria or parasites
Chemical carcinogens
Asbestos
Tobacco smoke
Human epidermal growth factor receptors
HER
Family of structurally-related cell surface proteins
HER proteins undergo a conformational change upon ligand binding
essential for dimerization and signalling
Exception HER2
HER2/HER3 pair has strongest mitogenic signalling
Signalling pathways
Ligand binding causes a conformational change which leads to dimerisation
Dimerisation activates the tyrosine kinase domain
HER2 is in a conformation which promotes dimerisation
Different combinations of receptors stimulate different signalling pathways
HER pathways:
Stimulate cell proliferation
Stimulates cell survival
Are anti apoptotic
Are proto-oncogenes
Can become oncogenic by
Over expression
Mutation
1984
Published that a mutant form of HER2 causes cancer in rats
HER2
Frequently amplified in breast cancer samples
Gene amplification
When DNA replication goes wrong the cell can end up with hundreds of copies of a gene
Normal cells are diploid so 2n
The copy number of a gene can be determine by using a technique called fluorescence in situ hybridisation
FISH
If the gene is a proto-oncogene like HER2 this can cause cancer
Gene amplification of HER2 leads to increased levels of the receptor
Normal breast tissue has around 20,000 copies per cell
Cancerous tissue can have up to 2 million copies per cell
Negative prognostic marker for several cancers
Over-expression of HER2 correlates with poor survival rates
Median survival for breast cancer patients without treatment
HER2 positive 3 years
HER2 normal 6-7 years
HER2 over-expressing breast cancer can be targeted using theraputic antibodies
Antibodies
Can be raised against nearly any protein
Are very specific
Binding can interfere with receptor signalling
Binding can target cells for destruction by the bodies immune system
First step in making a theraputic antibody
Making a monoclonal antibody
Process published in 1975
monoclonal antibodies recognise a single epitope on an antigen
As you have a cell line that makes that antibody, vast quantities of the antibody can be made
It was thought that monoclonal antibodies would revolutionise medicine
However, murine antibodies are not well tolerated in humans
This is solved by a process called humanisation
4D5
Treating HER2 overexpressing cells with 4D5 - which binds the extracellular domain of HER2 - inhibits their proliferation
Monoclonal antibody
Injecting mice with 4D5 surpresses tumour growth
Injected radio-labelled 4D5 targets HER2 positive breast cancer cells in women
Humanised version
Herceptin (Trastuzumab)
Herceptin
An IgG1 molecule consists of
2 heavy chains
2 light chains
Complementary determining regions(CDR's)
Hypervariable regions of the antibody
Involved in antigen binding
Up to 6 CDRs can be involved in binding an antigen
How its generated
1) Clone the murine heavy and light chain cDNA encoding 4D5
2) Clone the murine CDRs of 4D5 into human IgG1 heavy and light chain plasmids
3) The humanised antibody is then made by transfecting CHO cells with light chain and heavy chain plasmids
Future directions
Cancer returns in around 25% of women treated with herceptin/chemotherapy
The cancer is resistant to herceptin treatment
HER2 dimerisation inhibitors
Pertuzumab gained FDA approval in 2012
Used in combination with herceptin and chemotherapy
Increases disease free survival in HER2 positive metastatic cancer by 6 months
Antibody drug conjugates
Trastuzuman emtansine gained FDA approval in 2013
Delivers toxic drug to HER2 positive tumours
Increases overall survival by 6 months
Targeting other HER family members
Theraputic antibodies being developed against HER3
Media attachments
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