Page 1,2,3
(3/3) ou fichier pdf (1,5 meg)
Page 1,2,3
(3/3) or pdf file (1,5 meg)
The types of cancer seen in SLE beluga also differ widely from those seen in other cetaceans (Tables 2 and 3). Gastrointestinal epithelial cancers were the most frequent cancers seen in SLE beluga; in contrast, hemopoietic cancers are the most frequent types of cancer observed in other cetaceans (Tables 1-3). Only one of the 33 cancers (3%) seen in other cetaceans was a gastrointestinal epithelial cancer. Furthermore, no mammary gland cancers had been previously reported in other cetaceans, whereas three of these cancers have been reported in SLE beluga (23).
A single cancer was found in over 1,800 other cetaceans examined, and tumors were not found in approximately 50 beluga examined in the Canadian Arctic [D.J. St. Aubin, personal communication, cited in (22)]. Arctic data may not be fully representative, however, because the age of Arctic beluga was unknown and these were randomly selected live animals and not stranded animals that died spontaneously. A single benign tumor was observed in 55 slaughtered pilot whales in Newfoundland (24), and only two benign tumors (0.1%) were reported in 2,000 mysticetes (baleen whales) hunted in South Africa (19).
The present study can best be compared with studies on singly stranded cetaceans rather than with studies performed on cetaceans shot or caught singly or collectively in fishing gears. None of these studies have shown a cancer rate comparable to that of SLE beluga. Neoplasia was not observed in 86 small odontocetes stranded on the Oregon and California shoreline (20,21). Among 90 bottlenose dolphins (Tursiops truncatus) stranded along the Gulf coast of Texas from 1991 to 1998, two cancers (or 2%), a myelogenous leukemia and a bile duct carcinoma, were found (25). No cancers were found in 28 harbor porpoises stranded on the British coast (26). Three cancers were found during the postmortem examination of 422 odontocetes (or 0.7%) from British waters (27), and a retrovirus may have been the etiologic agent of five lymphomas observed in dolphins on the American East Coast (28).
Comparison with other species. In the Western world, cancer causes 23% of all deaths in humans, a percentage comparable to that seen in SLE beluga (29). In wild animal populations, cancer has not been reported as a major cause of mortality in adults, with the possible exception of virus-induced liver cancer in woodchuck and retrovirus-induced leukemia in rodents (30,31). Instead, trauma and starvation are among the most frequent causes of death (Figure 3) (32). Both viruses and carcinogenic contaminants have been suspected to cause a high prevalence of metastatic carcinomas in California sea lions (33).
In veterinary and human epidemiology, the number of individuals at risk must be known precisely in order to determine disease prevalence. This requirement explains why few epidemiologic cancer studies have been carried out in wild mammal populations, which are notoriously ill defined and/or widespread. SLE belugas are an exception in this regard. This population is reasonably well characterized, geographically isolated, and restricted to a relatively small area and has been the object of numerous censuses often carried out using different techniques (1,17,18). All censuses have provided similar results, so the population at risk--the denominator used to calculate the AR (15)--is reasonably well defined.
We compared the AR and the AAR with those of domestic animals and humans (Figure 4). The AR of cancer, of epithelial cancer of the proximal intestine, of gastric cancer, of gastrointestinal epithelial cancer, and of mammary cancer was generally higher in SLE beluga than in domestic animals seen in veterinary hospitals. For all types of cancer, with the exception of mammary gland cancer, the SLE beluga AAR was higher than that in all other animal species and in humans. The AAR of mammary gland cancer was the same as the rate seen in humans and was comparable to the rate seen in dogs examined in veterinary hospitals (Figure 4).
Figure 4. Adjusted annual rate (cases per 100,000) of cancer in the SLE beluga compared with that of humans and domestic animals (34,35,92-94). |
Paradoxically, the collection of epidemiologic data from the SLE population resembles more closely that of humans than that of domestic animals because the denominator used in human studies, like that used in SLE beluga, is derived from periodic census; in contrast, the data obtained from domestic animals originates from veterinary hospitals. Because the latter population comprises many (if not mostly) sick animals, the epidemiologic data from it are expected to contain a higher rate of animals with cancer than those of the general population of domestic animals (34,35).
In addition, free-ranging animals generally have a shorter life span than do domestic animals because of predation (including hunting by humans), harsh environmental conditions, and malnutrition. Older animals are more numerous in the pet animal population than in free-ranging animals because of the absence of adverse conditions and because of curative and preventive improvements in veterinary medicine (15). Because the risk of developing cancer increases with age, cancer rates in pet, zoo, and aquarium animals are expected to be higher than in free-ranging mammals (36).
Considered together, these observations indicate that cancer rates in domestic animals as shown in Figure 4 are overestimated. Yet for all cancer types, the AAR in SLE beluga is much higher than that observed in cattle, horse, and sheep examined in veterinary hospitals, higher than the rate observed in dogs and cats examined in veterinary hospitals, and higher than the rate in humans.
Possible etiologic factors. Cancer of the proximal intestine is rare in all animal species and in humans. It is frequent, however, in certain bovine and ovine populations in certain parts of the world where it has been etiologically associated with the ingestion of herbicides such as 2,4-dichlorophenoxyacetic acid (37-40).
In cattle, small intestinal cancers result from an interaction between exogenous carcinogens and viruses. Bovine papillomavirus type 4 causes papillomas in the bovine upper digestive tract. In cattle infected with that virus and fed with bracken fern (which contains powerful carcinogens), papillomas become malignant and are accompanied by intestinal adenomas and adenocarcinomas (37). A similar interplay between a virus and environmental carcinogenic compounds may be at work in SLE beluga, because gastric papillomatosis has been observed in a significant number of carcasses, and particles consistent with papillomaviruses have been observed in papillomas (5,41).
Carcinogens are present in the environment of SLE beluga and are likely ingested by these animals. The tissue benzo[a]pyrene concentrations of blue mussels were 200 times higher after their transplantation into the Saguenay River than before (42). The sediments of the Saguenay River, which is a part of the SLE beluga habitat, contain 500-4,500 ppb of total PAH (dry weight), a concentration level significantly higher than within Osaka harbor, where PAH concentrations are 2,870 ppb, and these compounds originate from aluminum smelters located upstream (Figure 5) (43).
Figure 5. Saguenay River, Québec, Canada. Polycyclic aromatic hydrocarbon concentration in sediments (parts per billion, dry weight) (43). Chimney icon: aluminum smelters. |
Belugas dig into sediments (44), and in the SLE they feed on significant amounts of bottom invertebrates (45). Invertebrates living in sediments contaminated by PAHs accumulate these compounds, in contrast to vertebrates (46). Probably because of this diet and this feeding behavior, benzo[a]pyrene DNA adducts have been detected in stranded SLE beluga tissue by acid hydrolysis of DNA followed by high-performance liquid chromatography (HPLC) and fluorescence detection, whereas they have not been detected in Arctic beluga tissue, which live in a presumably less contaminated environment (5,47). However, no differences between the two populations were observed in another study where livers were analyzed by 32P postlabeling (48). These apparently conflicting results are not surprising given that 32P postlabeling is highly sensitive for the detection of a variety of bulky DNA adducts but does not allow the precise identification of these compounds. In contrast, acid hydrolysis of DNA followed by HPLC and fluorescence detection allows the specific quantitation of benzo[a]pyrene diolepoxide, the ultimate carcinogenic form of benzo[a]pyrene. Considered together, these observations suggest that SLE beluga ingest PAHs present in benthic invertebrates, which may contribute to the elevated rate of digestive tract cancers seen in this population (5,22,49).
A causal relationship between intestinal adenocarcinoma and PAHs is further supported by the observation that in mice, chronic ingestion of coal tar mixtures (which contains benzo[a]pyrene) causes small intestinal adenocarcinoma, forestomach papilloma, and gastric carcinoma (50). In humans, the ingestion of smoked food (which contains benzo[a]pyrene) and cancer of the small intestine have been etiologically related (51).
Cytochrome P450 (CYP) present in the small intestinal epithelium is among the first and among the major enzyme molecules implicated in the biotransformation and subsequent detoxication or toxification of ingested xenobiotics, and high levels of intestinal CYP have been related with gastrointestinal cancer (52). In the rat small intestine, the highest CYP concentrations occur in the duodenum, and the most abundant CYP is CYP1A1, known to activate PAHs into carcinogenic metabolites. It is the most abundant inducible form, and its inducibility decreases dramatically from the duodenum to the ileum (53,54).
Cetaceans have high levels of CYP1A and low levels of CYP2B. Compared with Arctic beluga, SLE belugas have elevated levels of both types of enzymes, probably because CYP are induced by exposure to high levels of PCBs [reviewed by Muir et al. (7)]. Considered together, the above observations suggest that intestinal CYP1A levels are elevated in SLE beluga and that these high levels may trigger the development of intestinal cancer by activating ingested PAHs into carcinogenic compounds. Besides inducing CYP enzymes, PCBs are also known immunosuppressive compounds. The possibility that PCB-induced diminished immunosurveillance contributes to cancer etiology has been discussed elsewhere (55).
A relation between ingestion of carcinogens and cancer in wildlife is not without precedent. In bottom-dwelling fish, labial papilloma and liver cancer are strongly associated with chemical contamination of sediments (56). Lake whitefish (LWF) are the only salmonids feeding on benthic fauna. Tissue concentrations of organochlorine compounds (OC) and of heavy metals found in LWF living in the SLE are three to five times higher than those of sympatric fish species (including nonsalmonid bottom-dwelling species), and these high concentrations coincide with a high prevalence of liver cancer in LWF (57,58). Thus, beluga and LWF, two aquatic vertebrate species that widely diverge taxonomically, may both be affected by cancer because both feed on the bottom, an unusual feature within their respective taxonomic group.
Mammary gland cancers were the cause of death of three (7.7%) of the adult female beluga examined from 1983 to 1999 (23). Mammary gland cancers have not been reported in other marine mammals and are rare in herbivores, including cattle, which are phylogenetically close to cetaceans; only isolated cases have been reported in other free-ranging wildlife species (59,60). In contrast, these tumors are common in humans, domestic carnivores, and rodents. These cancers have been etiologically related with viruses only in rodents [although retroviral sequences have recently been found in human cancerous breast (61)]. In women, these cancers have been related etiologically with OCs and PAHs (62-64). Alternatively, or concurrently with OCs and PAHs, these tumors may develop because of the extended hormonal stimulation associated with the long pregnancy and lactation of cetaceans (65).
In the Saguenay-Lac Saint-Jean region, aluminum workers are affected by a high prevalence of lung and urinary bladder cancer. These cancers have been epidemiologically related with exposure to coal tar volatile components produced by the combustion of carbon anodes used for the electrolysis of aluminum (66,67). Elsewhere, gastric cancers have been also epidemiologically related with working in aluminum plants where carbon anodes are prebaked (68).
The incidence of cancer of the stomach, digestive tract, and breast is also higher in the Saguenay population that does not work in the aluminum industry (10) (Figures 1 and 5). This high cancer incidence could be related to the fact that the drinking water of 79% of the population comes from local surface water (rivers and lakes) and that large quantities of PAHs have been, and are, released locally into the atmosphere by local aluminum smelters (69,70). Because of cheap hydroelectricity and accessibility to the sea, aluminum smelters have been in operation in that region since as early as 1926. Between 1937 and 1980, 40,000 tons of PAHs generated by the aluminum smelters have accumulated in the fjord watershed, from which 20 tons are released per year and from which 3% are benzo[a]pyrene, a strong carcinogen (71). Both the magnitude and the persistence of this threat to public health have been clearly recognized (71).
Together, these observations suggest that a human population and a population of long-lived, highly evolved mammals may be affected by specific types of cancer because they share the same habitat and are exposed to the same environmental contaminants.
In people, genetic susceptibility to cancer takes two forms: hereditary cancer syndromes (HCSs) such as familial adenomatous polyposis, and population susceptibility, where an ensemble of individuals has an increased risk of cancer (but not as high as in HCSs). Because inbreeding has led to some degree of genetic homogeneity in SLE beluga, the possibility of an HCS within the SLE beluga population has to be considered (72). HCSs affect multiple--and most often young--members of a same family (73,74). Beluga with cancer were not younger than beluga dead of other causes (Table 1, Figure 2). In addition, other genetically homogeneous free-ranging or captive wildlife populations have not been found affected by high rates of cancer (75,76). An apparent exception is the highly inbred black-footed ferret (Mustela nigripes), where a high prevalence of cancers has been observed. However, all black-footed ferrets affected by cancer have been kept in captivity. Captivity greatly extends the life span of these animals, from 4 years in the wild to 7-9 years in captivity. Because all tumors develop only in ferrets older than 5 years, captivity clearly plays a major role in the etiology of these tumors by extending life span (77). In addition, these animals may have been exposed to carcinogenic compounds in captivity. Thus, there is no evidence supporting that cancer in SLE beluga is a hereditary cancer syndrome.
In population susceptibility to cancer, an ensemble of individuals has increased risk of developing cancer because these individuals have a specific and common genetic feature caused by normal polymorphism (73). This feature most often influences the metabolism of carcinogenic xenobiotics. It can be envisaged that some SLE beluga have highly induced CYP1A1 in the proximal intestinal epithelium, rendering cells susceptible to mutagenesis by DNA-damaging metabolites generated from specific xenobiotics such as benzo[a]pyrene.
There is no evidence that cancer is frequent in beluga as a species. A single case of cancer is listed among the 56 belugas listed in the Marine Mammal Database (Table 3). The few significantly prevalent cancers observed in wild mammals have a viral etiology.
Two lines of evidence are not consistent with the high rate of cancer being caused by old age. First, SLE beluga affected with cancer did not reach the maximum life span reached by Arctic beluga; and second, SLE beluga with cancer showed the same age distribution as did beluga dead of other causes (Figure 2).
Future studies. Few odontocetes species feed on benthic invertebrates: the Amazon river dolphin (Inia geoffrensis), the Franciscana (Phocoena blainvillei), the Susu (P. gangetica), and the Irrawaddy dolphin (Orcinus brevirostris) (78). Because these species generally inhabit rivers that are often more contaminated than the open ocean, high rates of cancers of the gastrointestinal tract may also be found in these species.
Several chemical carcinogens leave a signature on the host genome by causing mutations at specific sites in genes involved in cell proliferation, such as p53 and ras. The finding of the same signature in tumors of SLE beluga, fish, and humans would strongly support the etiologic role of contaminants in carcinogenesis (79,80).
Because cancer is an ultimate but rare consequence of chemical mutagenesis, the epidemiologic association of xenobiotics with carcinogenesis requires the examination of large numbers of animals. To demonstrate the role of xenobiotics in carcinogenesis in SLE beluga, convincing statistics would require much larger numbers of whales and/or the follow-up of SLE beluga for many more decades. The observation of high prevalences of cancer in other populations of marine mammals similarly exposed to carcinogens would strengthen an etiologic relationship with chemical carcinogenesis.
References and Notes
1. Lesage V, Kingsley MCS. Updated status of the St. Lawrence River population of the beluga, Delphinapterus leucas. Can Field Nat 112:98-113 (1998).
2. Reeves RR. Catch history and initial population of white whales (Delphinapterus leucas) in the River and Gulf of the St. Lawrence Eastern Canada. Can Field Nat 111:63-121 (1984).
3. Sergeant D. Present status of white whales (Delphinapterus leucas) in the St. Lawrence Estuary. Can Field Nat 113:61-81 (1986).
4. Letcher RJ, Norstrom RJ, Muir DCG, Sandau K, Koczanski R, Michaud R, De Guise S, Béland P. Methylsulfone PCB and DDE metabolites in beluga whale (Delphinapterus leucas) from the St. Lawrence River estuary and western Hudson Bay. Environ Toxicol Chem 19(5):1378-1388 (2000).
5. Martineau D, Lagacé A, Béland P, Higgins R, Armstrong D, Shugart L. Pathology of stranded beluga whales (Delphinapterus leucas) from the St. Lawrence estuary, Quebec. J Comp Pathol 98:287-311 (1988).
6. Martineau D, Béland P, Desjardins C, Lagacé A. Levels of organochlorine chemicals in tissues of beluga whales (Delphinapterus leucas) from the St. Lawrence estuary, Quebec, Canada. Arch Environ Contam Toxicol 16:137-147 (1987).
7. Muir DCG, Ford CA, Rosenberg B, Norstrom RJ, Simon M, Béland P. Persistent organochlorines in beluga whales (Delphinapterus leucas) from the St. Lawrence River estuary. I. Concentrations and patterns of specific PCBs, chlorinated pesticides and polychlorinated dibenzo-p-dioxins and dibenzofurans. Environ Pollut 93:219-234 (1996).
8. Wagemann R, Stewart REA, Béland P, Desjardins C. Heavy metals and selenium in tissues of beluga whales, Delphinapterus leucas, from the Canadian Arctic and the St. Lawrence estuary. In: Advances in Research on the Beluga Whale, Delphinapterus leucas (Smith TG, St. Aubin DJ, Geraci JR, eds). Ottawa:Dept. of Fisheries and Oceans, 1990;191-206.
9. Brodie PF. The beluga (Delphinapterus leucas); growth at age based on a captive specimen and a discussion of factors affecting natural mortality estimates. Rep Int Whal Comm 32:445-447 (1982).
10. Lebel G, Gingras S, Levallois P, Gauthier R, Gagnon M-F. Etude descriptive de l'incidence du cancer au Québec de 1989 à 1993, Beauport:Centre de Santé Publique de Québec, 1998.
11. Martineau D, Lair S, De Guise S, Lipscomb TP, Béland P. Cancer in beluga whales from the St. Lawrence estuary, Quebec, Canada: a potential biomarker of environmental contamination. J Cetacean Res Manag 1:249-265 (1999).
12. Béland P, Vézina A, Martineau D. Potential for growth of the St. Lawrence (Québec, Canada) beluga whale (Delphinapterus leucas) population based on modelling. ICES J Mar Sci (J Conseil) 45:22-32 (1988).
13. Alaska Department of Fish and Game. Investigations of Belukha Whales in Coastal Waters of Western and Northern Alaska. II. Biology and Ecology (Burns JJ, Seaman GA, eds). Contract NA 81 RAC 00049. Fairbanks, AK:Alaska Department of Fish and Game, 1986.
14. Martineau D, Lair S, De Guise S, Béland P. Intestinal adenocarcinomas in two beluga whales (Delphinapterus leucas) from the estuary of the St. Lawrence River. Can Vet J 36:563-565 (1995).
15. Dorn CR, Priester WA. Epidemiology. In: Veterinary Cancer Medicine (Theilen GH, Madewell BR, eds). Philadelphia:Lea & Febiger, 1987;27-52.
16. Michaud R, Béland P. Looking for trends in the endangered St. Lawrence beluga population. A critique of Kingsley, M.C.S. 1998. Population index estimates for the St. Lawrence beluga, 1973-1995. Mar Mamm Sci 17:206-212 (2001).
17. Michaud R. Distribution estivale du beluga du Saint-Laurent; synthèse 1986 à 1992. Department of Fisheries and Oceans Canada. Rapp Tech Can Sci Halieut Aquat 1906:1-22 (1993).
18. Kingsley MCS, Hammill MO. Photographic census surveys of the St. Lawrence population, 1988 and 1990. Department of Fisheries and Oceans Canada. Rapp Tech Can Sci Halieut Aquat 1776:1-19 (1991).
19. Uys CJ, Best PB. Pathology of lesions observed in whales flensed at Saldanha Bay, South Africa. J Comp Pathol 76:407-412 (1966).
20. Stroud RK, Roffe TJ. Causes of death in marine mammals stranded along the Oregon coast. J Wildl Dis 15:91-97 (1979).
21. Howard EB, Britt JO Jr, Simpson JG. Neoplasms in marine mammals. In: Pathobiology of Marine Mammal Diseases (Howard EB, ed). Boca Raton, FL:CRC Press, 1983;95-162.
22. De Guise S, Lagacé A, Béland P. Tumors in St. Lawrence beluga whales (Delphinapterus leucas). Vet Pathol 31:444-449 (1994).
23. Mikaelian I, Labelle P, Martineau D. Metastatic mammary adenocarcinomas in two beluga whales (Delphinapterus leucas) from the St. Lawrence estuary, Quebec, Canada. Vet Rec 145:738-739 (1999).
24. Cowan DF. Pathology of the pilot whale. Globicephala melaena. A comparative survey. Arch Pathol 82:178-189 (1966).
25. Cowan D. Involution and cystic transformation of the thymus in the bottlenose dolphin, Tursiops truncatus. Vet Pathol 31:648-653 (1994).
26. Kuiken T, Höfle U, Benett PM, Allchin CR, Kirkwood JK, Baker JR, Appleby EC, Lockyer CH, Walton MJ, Sheldrick MC. Adrenocortical hyperplasia, disease and chlorinated hydrocarbons in the harbour porpoise (Phocoena phocoena). Mar Pollut Bull 26:440-446 (1993).
27. Kirkwood JK, Bennett PM, Jepson PD, Kuiken T, Simpson VR, Baker JR. Entanglement in fishing gear and other causes of death in cetaceans stranded on the coasts of England and Wales. Vet Rec 141:94-98 (1997).
28. Bossart GD, Ewing R, Herron AJ, Cray C, Mase B, Decker SJ, Alexander JW, Altman NH. Immunoblastic malignant lymphoma in dolphins: histologic, ultrastructural and immunohistochemical features. J Vet Diagn Invest 9:454-458 (1997).
29. Cotran RS, Kumar V, Robbins SL, Schoen FJ. Neoplasia. In: Pathologic Basis of Disease (Cotran RS, Robbins SL, Kumar V, eds). Philadelphia:W.B. Saunders, 1994;241-304.
30. Teich N. Taxonomy of retroviruses. In: RNA Tumor Viruses (Weiss R, Teich N, Varmus H, Coffin J, eds). Cold Spring Harbor, NY:Cold Spring Harbor Laboratory, 1984;25-209.
31. Snyder RL, Tyler G, Summers J. Chronic hepatitis and hepatocellular carcinoma associated with woodchuck hepatitis virus. Am J Pathol 107:422-425 (1982).
32. Aguirre AA, Brojer C, Morner T. Descriptive epidemiology of roe deer mortality in Sweden. J Wildl Dis 35:753-762 (1999).
33. Lipscomb TP, Scott DP, Garber RL, Krafft AE, Tsai MM, Lichy JH, Taubenberger JK, Schulman FY, Gulland FM. Common metastatic carcinoma of California sea lions (Zalophus californianus): evidence of genital origin and association with novel gammaherpesvirus. Vet Pathol 37:609-617 (2000).
34. Priester WA, McKay FW. The Occurrence of Tumors in Domestic Animals. Bethesda, MD:U.S. Department of Health and Human Services, Public Health Service, National Institutes of Health, National Cancer Institute, 1980.
35. MacVean DW, Monlux AW, Anderson PS Jr, Silberg SL, Roszel JF. Frequency of canine and feline tumors in a defined population. Vet Pathol 15:700-715 (1978).
36. Fowler ME. Zoo animals and wildlife. In: Veterinary Cancer Medicine (Theilen GH, Madewell BR, eds). Philadelphia:Lea & Febiger, 1987;649-662.
37. Campo MS, O'Neil BW, Barron RJ, Jarrett WF. Experimental reproduction of the papilloma-carcinoma complex of the alimentary canal in cattle. Carcinogenesis 15:1597-1601 (1994).
38. Cordes DO, Shortridge EH. Neoplasms of sheep: a survey of 256 cases recorded at Ruakura Animal Health Laboratory. NZ Vet J 19:55-64 (1971).
39. Jarrett WHF, McNeil PE, Grimshaw WTR, Selman IE, McIntyre WIM. High incidence area of cattle cancer with a possible interaction between an environmental carcinogen and a papillomavirus. Nature 274:215-217 (1978).
40. Newell KW, Ross AD, Renner RM. Phenoxy and picolinic acid herbicides and small-intestinal adenocarcinoma in sheep. Lancet 2:1301-1305 (1984).
41. De Guise S, Lagacé A, Béland P. Gastric papillomas in eight St. Lawrence beluga whales (Delphinapterus leucas). J Vet Diagn Invest 6:385-388 (1994).
42. Cossa D, Picard-Bérubé M, Gouygou J-P. Polynuclear aromatic hydrocarbons in mussels from the estuary and northwestern gulf of St. Lawrence, Canada. Bull Environ Contam Toxicol 31:41-47 (1983).
43. Martel LM, Gagnon J, Massé R, Leclerc A, Tremblay L. Polyclyclic aromatic hydrocarbons in sediments from the Saguenay fjord, Canada. Bull Environ Contam Toxicol 37:133-140 (1986).
44. Dalcourt MF, Béland P, Pelletier E, Vigneault Y. Caractérisation des communautés benthiques et étude des contaminants dans des aires fréquentées par le béluga du Saint-Laurent. Department of Fisheries and Oceans Canada. Rapp Tech Can Sci Halieut Aquat 1845:1-86 (1992).
45. Vladykov VD. Études sur les Mammifères Aquatiques IV. Nourriture du Marsouin Blanc ou Béluga (Delphinapterus leucas) du Fleuve Saint-Laurent. Contribution du Département Pêcheries du Québec, 1946.
46. Ferguson PL, Chandler GT. A laboratory and field comparison of sediment polycyclic aromatic hydrocarbon bioaccumulation by the cosmopolitan estuarine polychaete Streblospio benedicti (Webster). Mar Environ Res 45:387-401 (1998).
47. Shugart LR, Martineau D, Béland P. Detection and quantitation of benzo[a]pyrene adducts in brain and liver tissue of beluga whales (Delphinapterus leucas). In: Proceedings of the International Forum for the Future of the Beluga. Tadoussac, Québec, Canada (Prescott J, Gauquelin M, eds). Sillery:Presses de l'Université du Québec, 1990;219-223.
48. Ray S, Dunn BP, Payne JF, Fancey L, Helbig R, Béland P. Aromatic DNA-carcinogen adducts in beluga whales from the Canadian Arctic and Gulf of St. Lawrence. Mar Pollut Bull 22:392-396 (1991).
49. Martineau D, De Guise S, Fournier M, Shugart L, Girard C, Lagace A, Beland P. Pathology and toxicology of beluga whales from the St. Lawrence estuary, Quebec, Canada. Past, present and future. Sci Total Environ 154:201-215 (1994).
50. Culp SJ, Gaylor DW, Sheldon WG, Goldstein LS, Beland FA. A comparison of the tumors induced by coal tar and benzo[a]pyrene in a 2-year bioassay. Carcinogenesis 19:117-124 (1998).
51. Chow WH, Linet MS, McLaughlin JK, Hsing AW, Cochien HT, Blot WJ. Risk factors for small intestine cancer. Cancer Causes Control 4:163-169 (1993).
52. Kaminsky LS, Fasco MJ. Small intestinal cytochromes P450. Crit Rev Toxicol 21:407-422 (1991).
53. Zhang QY, Wikoff J, Dunbar D, Kaminsky L. Characterization of rat small intestinal cytochrome P450 composition and inducibility. Drug Metab Dispos 24:322-328 (1996).
54. Zhang QY, Wikoff J, Dunbar D, Fasco M, Kaminsky L. Regulation of cytochrome P4501A1 expression in rat small intestine. Drug Metab Dispos 25:21-26 (1997).
55. Béland P, De Guise S, Girard C, Lagacé A, Martineau D, Michaud R, Muir DCG, Norstrom RJ, Pelletier E, Ray S, et al. Toxic compounds and health and reproductive effects in St. Lawrence beluga whales. J Gt Lakes Res 19:766-775 (1993).
56. Harshbarger JC. Invertebrate and cold-blooded vertebrate oncology. In: Spontaneous Animal Tumors: A Survey (Rossi L, Richardson R, Harshbarger JC, eds). Milano, Italy:Press Point, 1997;41-53.
57. Mikaelian I, de Lafontaine Y, Menard C, Tellier P, Harshbarger J, Martineau D. Neoplastic and nonneoplastic hepatic changes in lake whitefish (Coregonus clupeaformis) from the St. Lawrence River, Quebec, Canada. Environ Health Perspect 106:179-183 (1998).
58. Mikaelian I, de Lafontaine Y, Harshbarger JC, Lee LLJ, Martineau D. Health of lake whitefish (Coregonus clupeaformis) with elevated tissue levels of environmental contaminants. Environ Toxicol Chem (In press, 2002).
59. Veatch JK, Carpenter JW. Metastatic adenocarcinoma of the mammary gland in a Père David's deer. J Vet Diagn Invest 5:639-640 (1993).
60. Gillete DM, Acland HM, Klein L. Ductular mammary carcinoma in a lioness. J Am Vet Med Assoc 173:1099-1102 (1978).
61. Pogo BG, Melana SM, Holland JF, Mandeli JF, Pilotti S, Casalini P, Menard S. Sequences homologous to the mouse mammary tumor virus env gene in human breast carcinoma correlate with overexpression of laminin receptor. Clin Cancer Res 5:2108-2111 (1999).
62. Blackwood A, Wolff M, Rundle A, Estabrook A, Schnabel F, Mooney LA, Rivera M, Channing KM, Perera F. Organochlorine compounds (DDE and PCB) in plasma and breast cyst fluid of women with benign breast disease. Cancer Epidemiol Biomarkers Prev 7:570-583 (1998).
63. Güttes S, Failing K, Neumann K, Kleinstein J, Georgii S, Brunn H. Chlororganic pesticides and polychlorinated biphenyls in breast tissue of woman with benign and malignant breast disease. Arch Environ Contam Toxicol 35:140-147 (1998).
64. Perera FP, Estabrook A, Hewer A, Channing K, Rundle A, Mooney LA, Whyatt R, Phillips GN. Carcinogen-DNA adducts in human breast tissue. Cancer Epidemiol Biomarkers Prev 4:233-238 (1995).
65. Geraci JR, Palmer NC, St Aubin DJ. Tumors in cetaceans: analysis and new findings. Can J Fish Aquat Sci 44:1289-1300 (1987).
66. Armstrong B, Tremblay C, Baris D, Theriault G. Lung cancer mortality and polynuclear aromatic hydrocarbons: a case-cohort study of aluminum production workers in Arvida, Quebec, Canada. Am J Epidemiol 139:250-262 (1994).
67. Tremblay C, Armstrong B, Theriault G, Brodeur J. Estimation of risk of developing bladder cancer among workers exposed to coal tar pitch volatiles in the primary aluminum industry. Am J Ind Med 27:335-348 (1995).
68. Bye T, Romundstad PR, Ronneberg A, Hilt B. Health survey of former workers in a Norwegian coke plant. Part 2. Cancer incidence and cause specific mortality. Occup Environ Med 55:622-626 (1998).
69. Saint-Laurent Vision 2000. Synthèse des connaissances sur les aspects socio-économiques du Saguenay. Rapport technique. Zones d'intervention prioritaire 22 et 23. Centre Saint-Laurent. Environnement Canada. Région du Québec. Saint-Laurent Vision 2000. En40-216/14F. Montreal, Quebec:Centre Saint-Laurent Environnement Canada, 1995.
70. Saint-Laurent Vision 2000. Synthèse des connaissances sur les aspects physiques et chimiques de l'eau et des sédiments du Saguenay. Rapport technique. Zones d'intervention prioritaire 22 et 23. Centre Saint-Laurent. Environnement Canada. Région du Québec. Saint-Laurent Vision 2000. En40-216/17F. Montreal, Quebec:Centre Saint-Laurent Environnement Canada, 1995.
71. Smith MC, Levy EM. Geochronology for polycylic aromatic hydrocarbon contamination in sediments of the Saguenay fjord. Environ Sci Technol 24:874-879 (1990).
72. Patenaude NJ, Quinn JS, Béland P, Kingsley M, White BN. Genetic variation of the St. Lawrence beluga whale population assessed by DNA fingerprinting. Mol Ecol 3:375-381 (1994).
73. Fearon ER. Human cancer syndromes: clues to the origin and nature of cancer. Science 278:1043-1050 (1997).
74. Perera FP. Environment and cancer: who are susceptible? Science 278:1068-1073 (1997).
75. Munson L, Nesbit JW, Meltzer DG, Colly LP, Bolton L, Kriek NP. Diseases of captive cheetahs (Acinonyx jubatus jubatus) in South Africa: a 20-year retrospective survey. J Zoo Wildl Med 30:342-347 (1999).
76. O'Brien SJ. A role for molecular genetics in biological conservation. Proc Natl Acad Sci USA 191:5748-5755 (1994).
77. Lair S. Epidemiology and pathology of neoplasia in the captive population of the black-footed ferret (Mustela nigripes) [DVSc]. Guelph, Ontario:University of Guelph, 1998.
78. Ridgway SH, Harrison R, eds. Handbook of Marine Mammals. San Diego:Academic Press, 1989;1-101.
79. Perera FP. Molecular epidemiology of environmental carcinogenesis. Recent Results Cancer Res 154:39-46 (1998).
80. Perera FP, Dickey C. Molecular epidemiology and occupational health. Ann NY Acad Sci 837:353-359 (1997).
81. Girard C, Lagacé A, Higgins R, Béland P. Adenocarcinoma of the salivary gland in a beluga whale (Delphinapterus leucas). J Vet Diagn Invest 3:264-265 (1991).
82. Lair S, De Guise S, Martineau D. Uterine adenocarcinoma with abdominal carcinomatosis in a beluga whale. J Wildl Dis 34:373-376 (1998).
83. Martineau D, Lagacé A, Massé R, Morin M, Béland P. Transitional cell carcinoma of the urinary bladder in a beluga whale (Delphinapterus leucas). Can Vet J 26:297-302 (1985).
84. Landy RB. A review of neoplasia in marine mammals (Pinnepedia and Cetacea). In: The Comparative Pathology of Zoo Animals (Montali RJ, Migaki G, eds). Washington, DC:Smithsonian Institution Press, 1980;579-591.
85. Cowan D. Personal communication.
86. Benirschke K, Marsh H. Anatomic and pathologic observations of female reproductive organs in the short-finned pilot whale, Globicephala macrorhynchus. Rep Int Whal Comm 6:451-454 (1984).
87. Baker JR. Causes of mortality and parasites and incidental lesions in dolphins and whales from British waters. Vet Rec 130:569-572 (1992).
88. Breuer EM, Krebs BH, Hofmeister RJ. Metastasizing adenocarcinoma of the stomach in a harbor porpoise. Dis Aquat Org 7:159-163 (1989).
89. Rewell RE, Willis RA. Some tumours found in whales. J Pathol Bacteriol 61:454-456 (1949).
90. Stolk A. Tumours in whales. Amsterdam Nat 1:28-33 (1950).
91. Yonezawa M, Nakamine H, Tanaka T, Miyaji T. Hodgkin's disease in a killer whale (Orcinus orca). J Comp Pathol 100:203-207 (1989).
92. Gaudette LA, Altmayer CA, Wysocki M, Gao R-N. Cancer Incidence and Mortality across Canada. Catalogue No. 82-003. Ottawa:Statistics Canada Health Reports, 1998.
93. Health Canada. Cancer in Canada. 1985, 1986, Vol 3, No. 2. Ottawa:Health Canada, 1991.
94. Georgsson G, Vigfusson H. Carcinoma of the small intestine of sheep in Iceland. A pathological and epizootiological study. Acta Vet Scand 14:392-409 (1973).
Page 1,2,3
(3/3) ou fichier pdf (1,5 meg)
Page 1,2,3
(3/3) or pdf file (1,5 meg)
Last Updated: February 12, 2002