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BHCS2004 - Cell Biology in Health and Disease - Cancer Cell Biology Summary $10.43   Add to cart

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BHCS2004 - Cell Biology in Health and Disease - Cancer Cell Biology Summary

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A complete summary of the cancer cell biology aspect of the BHCS2004 Cell biology in health and disease module at University of Plymouth.

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  • November 10, 2023
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  • 2023/2024
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Cancer Cell Biology



What Causes Cancer

 Environmental carcinogens cause mutation

 DNA damage and mutations are also caused by endogenous factors produced by normal
cellular metabolism

 DNA damage can lead to mutations

o UV light commonly induces cyclobutene pyrimidine dimers (CPD)

o Cytosine residues with CPD deaminate into uracil

o This induces a C > T mutation



DNA Damage Repair

 5 main pathways for repair

o Direct repair

o Base excision repair

o Nucleotide excision repair

o Mismatch repair

o Double stranded break repair

 Inherited defects in these pathways increase the risk of cancer



Nucleotide Excision Repair Mutations

 Mutations cause Xeroderma pigmentosum

 Autosomal recessive disease with very high risk of skin cancer

 NER is the only pathway to remove UV-induced pyrimidine dimers in humans

 16 NER proteins in humans



Types of Mutations

 Germline mutations

o Present in eggs or sperm

o Are heritable

o Causes hereditary cancer

,  Somatic mutations

o Occur in non-germline tissues

o Are non-heritable

o Later onset



Gene Mutations

 Oncogene

o A gene that played a normal role in the cell that has been altered by mutation and
now may contribute to growth of tumour

 Tumour suppressor genes

o A protective gene that normally limits the growth of tumour

 Gatekeepers

o Genes that directly regulate tumour growth by inhibiting tumour growth or
preventing death

 Caretakers

o Inactivation leads to genomic instability and increased risk of mutation in all genes



Knudson’s 2-hit Hypothesis

 That tumour suppressor genes require both alleles to be inactivated to cause a phenotypic
change



Cancer Hallmarks

 Evading growth suppression

 Avoiding immune destruction

 Enabling replicative immortality

 Tumour promoting inflammation

 Activating invasion and metastasis

 Inducing or accessing vasculature

 Genome instability and mutation

 Resisting cell death

 Deregulating cellular metabolism

 Sustaining proliferative signalling

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