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Environmental Health Carcinogenesis

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Title: Environmental Health Carcinogenesis


1
Environmental Health Carcinogenesis
  • Week 7

2
Genotoxicity toxic effects on genetic material
  • Cancer
  • Developmental
  • (gestational timing crucial)
  • Somatic diseases

3
The nature of life information
  • DNA structure
  • Base-sugar-triphosphate
  • Purines A, G Pyrimidines C, T(U)
  • Double helix A-T C-G pairs
  • Chromosomes (with chromatin)
  • Humans 23 autos. pairs sex pair (XY, XX)
  • DNA (code) --gt protein 3nucleic acids /1
    aminoacid
  • Universal code - the same principles and
    molecules in every organism (amoebas to humans)
  • Genes (units of information) are the same in
    every cell of an organism, but expression of
    genes varies by cell/tissue
  • Conserved and variable regions of code

4
Types of Genotoxic effects
  • Chromosomal aberrations
  • Deletions
  • Duplications
  • Inversions
  • Translocations
  • Sister chromatid exchanges
  • Gene mutations
  • Point mutations (base replacement)
  • Frameshift mutations
  • (insertion/deletion of part of gene)

5
Mutagensagents that cause a mutation
  • Mutation Alteration in the genetic code (DNA
    sequence of nucleotides), that may result in
    altered population of cells or organisms (nucleic
    DNA most important)
  • Mutations
  • Adaptation/survival and speciation
  • Disease and death

6
Effects of mutations
  • Silent - no effect
  • Change in gene expression
  • protein amount, location, timing
  • Change in structure of protein
  • Single aminoacid change (especially
    hydrophilic-phobic)
  • Multiple aminoacids/Trancation
  • Change or loss of activity
  • Inefficient or improper biochemical process
  • Altered cell function
  • Disease cancer birth defects hereditary
    diseases

7
Genotoxic factors
  • UV light (200-300nm) (gt10-10m)
  • Thymine dimerization (T-T)
  • Cytosine hydration (C H2O)
  • Ionizing radiation
  • (x/ ? -rays, lt10-10m ?, ? particles)
  • Single strand, double strand breaks, base changes
  • Biotoxins (aflatoxin-B1)
  • Viruses (HPV)

8
More genotoxic factors
  • Chemicals
  • Alkylating (diethylnitrosamine)
  • Mispairing (G-T vs G-C)
  • Depurination (transition, transversion)
  • Backbone break
  • Arylating (forming DNA adducts)
  • Intercalating (planar aromatic hydrocarbons)
  • Base analogues (5-Br-uracil 5-F-uracil)
  • Metaphase blockers
  • Deamination agents
  • Enzyme inhibitors
  • Metals (As, Be, Cd, Cr(IV, V), Ni, Pb)

9
Types of DNA damage
10
Reactive oxygen species
11
Post genetic-damage events
  • Repair
  • Apoptosis
  • Permanent change
  • Cell level
  • Tissue level
  • Organism level
  • Species level

See also p. 64 and 262 of Casarett and Doulls
Toxicology
12
Extensive DNA repair system
13
Cancer, a.k.a. malignant neoplasm
  • Uncontrolled growth and spread of abnormal cells
  • Solid tumors liver, lung, intestine, breast, etc
  • Blood and lymphatic system, incl. bone marrow
  • Reasons for increased cancer incidence
  • increased age
  • increased number of carcinogens present
  • other?

14
Cancer is the leading disease-related cause of
years of life lost in the US.
  • Causes of Death
  • All causes
  • Unintentional injuries
  • Cancer
  • Heart disease
  • Suicide, homicide
  • Congenital anomalies
  • Years of Life Lost
  • 11,761,000
  • 2,306,000
  • 1,803,000
  • 1,563,000
  • 1,247,000
  • 584,000

Estimated years of life lost before the age of
65
15
Carcinogenesis Terms
  • Chemical Carcinogenesis is the chemically-induced
    generation of cancerous growths in living
    organisms. Cancerous growths are often called
    neoplasms.
  • A neoplasm is an abnormal tissue mass, the growth
    of which exceeds and is uncoordinated with that
    of normal tissue and persists in a similar manner
    following cessation of stimulus. Unique feature
    is the continuous replication of a cell
    population.

16
Cancer is therefore the malignant uncontrolled
proliferation of neoplastic cells. Also a
description of a multitude of different disease
states (200)
17
Malignant vs. Benign Neoplasms
  • Benign
  • Usually encapsulated
  • Usually non-invasive
  • Highly differentiated
  • Rare mitoses
  • Slow growth
  • Little or no anaplasia
  • No metastases
  • Malignant
  • Encapsulated
  • Invasive
  • Poorly differentiated
  • Mitoses relatively common
  • Rapid growth
  • Anaplastic to varying degrees
  • Metastases

18
The many faces of cancer
Malignant neoplasms are usually called
carcinomas (endo- or ectoderm) or
sarcomas (mesoderm). Exceptions are hematopoietic
malignancies, melanoma, neuroblastoma, thymoma.
19
Carcinogens
  • Genotoxic Non-genotoxic

20
Many different chemical structures are
carcinogenic
21
Natural/endogenous molecules with carcinogenic
properties
22
Synthetic hormone-like structures
23
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24
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25
Millers showed that metabolic activation is key
to carcinogenicity (1950s)
26
metabolic activation, continued
27
Activation can occur also following Phase II
reactions
28
Reactive metabolites bind covalently to DNA and
form adducts which can generate mutations
29
adducts, continued
30
adducts, continued
31
Effective elimination of carcinogens is a means
of protection
32
Carcinogenesis
  • Initiation
  • Dose related
  • Dividing cells in site are targets
  • Genetic damage on expressed genes
  • Can be repaired
  • Promotion
  • Activation of initiated cell
  • First cell of tumor
  • Progression
  • Rapid (relatively) expansion of abnormal cells

See also p. 267, 271, 275 of Casarett and Doulls
Toxicology
33
Initiation and promotion
34
Polyaromatic hydrocarbons (PAHs) are initiating
agents in tumor development
35
Tumor promoters TPA is the experimental skin
tumor promoter found in croton oil
36
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37
Liver tumor incidence after daily doses of
2-acetylaminofluorene
38
Tumor response on mice initiated with 0.2?mol of
dimethylbenzanthracene and promoted with
12-O-tetradecanoylphorbol-13-acetate
39
Potency of carcinogens
  • Defined as the slope of the dose-response curve
    for induction of neoplasms
  • Iball index ( animals with tumors)
  • TD50 (used in comparative list)
  • T25 (dose rate that gives 25 of neoplasms at
    specific site)

See also p. 301 of Casarett and Doulls
Toxicology
40
Clonal Selection Model of Neoplastic Progression
41
The multistep pathway to colorectal cancer
By B. Vogelstein
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