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Paolo Vineis Imperial College London Causal models of carcinogenesis: a historical perspective

Paolo Vineis Imperial College London Causal models of carcinogenesis: a historical perspective. 1. Models of carcinogenesis 2. Examples: smoking, asbestos 3. Role of mutation, cell selection, epigenetics 4. Causal models.

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Paolo Vineis Imperial College London Causal models of carcinogenesis: a historical perspective

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  1. Paolo Vineis Imperial College LondonCausal models of carcinogenesis: a historical perspective

  2. 1. Models of carcinogenesis2. Examples: smoking, asbestos3. Role of mutation, cell selection, epigenetics4. Causal models

  3. Armitage and Doll in 1954 proposed a multistage model based on the observation that the incidence rate of most epithelial tumors rises with a power of age (5-6th power). They hypothesized:- that cancer is not due to age itself but to prolonged duration of exposure to carcinogens- that for a life-long exposure an increase with a power of 6 means that there are 6 stages in carcinogenesis- for discontinued exposures the model becomes more complex

  4. I(t)= r1r2 … r(n-1) (t-w)n-1where r is the transition rate from a stage to the followingt is agew is the time mecessary to last-stage cells to give rise to a clinically overt cancerAs an approximation:I(t)=K t n-1(n-1) refers to the transition rates

  5. The relationship with age holds true for most epithelial cancers (exponential of age: 6 for oesophagus, stomach, pancreas, bladder, rectum, colon), but not for lung and breast (cohort phenomena)THE BASIC IDEA IS THAT IT IS NOT AGE BUT DURATION OF EXPOSURE

  6. EXPERIMENTS BY IVERSEN: TREATMENT OF MICE WITH DMBA (CARCINOGENESIS, 1991) A SINGLE DOSE OF 51.2 MICROGRAMS GAVE A TUMOR RATE OF 40%, WHILE THE SAME DOSE DIVIDED INTO 50 DOSES OF 1 MICROGRAM GAVE A 100% RATE

  7. REPEATED EXPOSURE TO SMALL DOSES SEEMS TO BE THE MOST HAZARDOUS SITUATION OBSERVED TO EXPECTED RATIO: ACETONE 0.04 DMBA 51.2 MICROG 0.62 25.6, TWICE 1.74 10, 6 TIMES 2.93 2.6, 20 TIMES 7.04 1, 50 TIMES 7.95 EXPERIMENTS WITH UV LIGHT IN MICE SHOWED THAT CONTINUOUS EXPOSURE AT LOW DOSES WAS MOST EFFECTIVE AN INCREASING TIME INTERVAL BETWEEN EACH DOSE MAY ALSO INCREASE THE RISK

  8. TOBACCO SMOKINGEXAMPLE: ACS COHORT (Hammond et al, 1977)Age at start SMR NNON-SMOKERS 1.025+ 3.2 2020-24 9.7 11015-19 12.8 315<15 15.1 101Years since cessation (20 cigs/day)0 13.7 351<1 29.1 331-4 12.0 335-9 7.2 2210+ 1.0 5

  9. EXAMPLE: ASBESTOS (Seidman et al, 1977)Years since cessation: % increase of CI5-9 -0.210-14 0.415-19 1.220-24 1.325-30 1.7

  10. On this basis, tobacco smoking has been considered to be both an early and a late stage carcinogen by Doll (1978) and Day and Brown (1980)while asbestos has been considered an early stage carcinogen for mesothelioma (risk never decreases after cessation, age at start is extremely important)

  11. Other models introduce different assumptions:(a) clonal expansion (Cairns 1975; Moolgavkar)(a) killing of stem cells (Cairns 2002)

  12. Multistage carcinogenesis and the incidence of colorectal cancer E. Georg Luebeck and Suresh H. Moolgavkar PNAS | November 12, 2002 | vol. 99 | no. 23 | 15095-15100 The TSCE model posits that a malignant cell arises after two rare events in a stem cell. After the first event,assumed to occur with rate µ1 per cell per year, the initiatedtem cell expands clonally, giving rise to an intermediate (initiated)lesion. Initiated stem cells divide symmetrically with rate alpha and die or differentiate with rate beta. With rate µ2, however, aninitiated cell may divide asymmetrically, giving rise to a malignantdaughter cell, the progenitor of a carcinoma. The growthof the intermediate lesion is described mathematically by a stochasticbirth-death process

  13. SELECTION IN CANCER: usual view It is commonly recognized that somatic MUTATION (irreversible change in DNA information content) initiates the process of carcinogenesis The mutated cell(s) are selected in vivo because of their growth advantage, loss of contact inhibition, loss of apoptotic pathway(s), etc. This is selection after mutation, i.e. SELECTION FOR THE MUTANT PHENOTYPE. (R Albertini)

  14. SELECTION FOR MUTANT PHENOTYPES IS ALSO SELECTION FOR MUTATOR PHENOTYPES(current view)

  15. CHILDREN TREATED FOR LEUKEMIA • Treatments included multiple cytotoxic and genotoxic agents • All treatments included a purine analogue, e.g. 6-MP, 6-TG

  16. Proliferation of Mutators in a Cell PopulationMao EF, Lane L, Lee J & Miller JHJournal of Bacteriology (1997)Vol 179 (2): 417-422

  17. IN HUMANS, AS IN BACTERIA, SELECTION FOR MUTANT PHENOTYPES IS ALSO SELECTION FOR MUTATOR PHENOTYPES(WHICH ARE PRESENT AT LOW FREQUENCIES IN MOST INDIVIDUALS)(R. Albertini)

  18. A NON-CANCER MODEL OF DARWINIAN MECHANISM: PNH Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired stem cell disorder characterized by intravascular hemolysis, and bone marrow failure. The characteristic defect in PNH is the somatic mutation of the PIG-A gene in hematopoietic cells.

  19. The current hypothesis explaining the disorder suggests that there are two components: (1) hematopoietic stem cells with the characteristic defect are present in the marrow of many if not all normal individuals in very small numbers; (2) some aplastogenic influence suppresses the normal stem cells but does not suppress the defective stem cells, thus allowing the proportion of these cells to increase. (“darwinian” interpretation) Bessler M, Mason P, Hillmen P, Luzzatto L. Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria.Lancet 1994 Apr 16;343(8903):951-3

  20. A new paradigm:epigenetics

  21. Information heritable during cell division other than the DNA sequence itself.

  22. Models of causality: from simple to complex

  23. Necessary and sufficient causes Necessary YesNo YesChr 21 Guillotine Down syndr. Cut neck Sufficient NoMycobacterium Tobacco Pulmonary TB Lung cancer (R Saracci, 2005)

  24. What about genetic causation? Necessary YesNo Yes two Rb XP-related mutations cancer Sufficient No one Rb All others mutation

  25. Insufficient Non-redundant component of an Unnecessary Sufficient Complex (INUS)

  26. ‚ ƒ  Use of graphical models to disentangle complex GEI (Vineis et al, paper in preparation)

  27. What is interaction?

  28. The absent minded Mr Smith A. the probability that Mr Smith leaves the gas alight is 50%, or p(A) = 0.5 (“environmental exposure”) B. the probability that the alarm system does not work is 1%, or p(B) = 0.01 (“genetic risk”) C. the probability that a fire develops for reasons other than those considered here (the “background risk”) is 1/1,000, or p(not A and not B) = p(C) = 0.001

  29. 1. The scenario of population average (prior probability). The probability of a fire occurring through the causal chain involving only two factors is: p(A and B) - p(not A and not B) = (0.5 x 0.01)-0.001= 0.005-0.001=0.004. The relative risk of a fire occurring through this chain, compared to the risk of fire through some other causal chain (C, the “background risk”) is 0.005/0.001=5.

  30. 2. A scenario of partial knowledge of individual risk. If Mr Smith knows that he left the gas on but he does not know if the alarm works, then the probability of a fire is: p(B given A) - p(non-A and non-B) = 0.01 - 0.001 = 0.009. The relative risk for this causal chain compared to the background risk is 0.01/0.001 = 10. 3. The scenario of perfect knowledge of extrinsic and intrinsic risk factors. If Mr Smith knows both that he left the gas on AND that the alarm does not work, then the probability of a fire is 1; the probability that the fire arises as a consequence of this particular causal chain is 1 - 0.001, and the relative risk is 1/0.001 = 1000.

  31. What really counts is the combination of factors, and in particular the fact that some exposures can “complete an incomplete causal chain”. What makes this insight particularly important for the problem of attributing causes of cancer (or any other disease) is that while we are confident that multiple factors act through causal chains such as these, we are almost always quite ignorant about what components make up these chains. (Vineis and Kriebel, Enviromental Health, 2006)

  32. My favourite approach: Schaffner’s “conditionalized realism” A theory is “true” conditionally on: Truth of auxiliary hypotheses (e.g. data in animals, molecular biology) Lack of valid alternative explanations Role of “middle range theories” (eg cell selection) Also: Wesley Salmon’s idea of “propagation of a mark” contributes to seeing causal inference as mutual support between different layers of reality (molecules to populations)

  33. Summary 1(a) different mathematical models are compatible witht the evidence on age-specific cancer incidence(b) different biological models (e.g. involving clonal expansion or stem cell death) are compatible with epidemiologic evidence(c) however, it is likely that selection of mutated clones AND of clones with mutator phenotype is involved(d) a rapidly expanding new paradigm based on epigenetics is now developing

  34. Summary 2 Different epistemological models are compatible with the evidence, except a naive one based on necessary and sufficient causes (a) Mackie's model of INUS (b) Salmon's propagation of a mark (c) Shaffner's multilayer model based on “middle-range” theories and conditionalized realism (d) a Bayesian approach to interaction

  35. THE END

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