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Circulating Mice and Viruses

The Jackson Memorial Laboratory, the National Cancer Institute, and the Genetics of Breast Cancer, 1930–1965

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The Practices of Human Genetics

Part of the book series: Sociology of the Sciences ((SOSC,volume 21))

Abstract

The issue of Nature Genetics published in October 1992 included a review on breast cancer genes. There M.C. King argued that breast cancer is one of the most common genetic diseases in the industralized world1. Such an interest in genetic predispositions to the formation of mammary tumor was hardly visible in the 1960s and 1970s. Debates on the genetics of cancer were more fashionable before World War II, however. For example, in 1932, M.T. Macklin, a preeminent advocate of eugenics, was asking physicians to pay serious attention to “evidence that tumors, both benign and malignant, are inherited in man”.2

Hegel remarks somewhere that all facts and personages of great importance in world history occur, as it were, twice. He forgot to add: the first time as a tragedy, the second as farce. Cousidières for Danton, Louis Blanc for Robespierre, the Montagne of 1848 to 1851 for the Montagne of 1793 to 1795, the Nephew for the Uncle.

Mass production is not merely quantity production, for this may have none of the requisites of mass production. Nor it is merely machine production, which also may exist without any resemblance to mass production. Mass production is the focusing upon a manufacturing project of the principles of power, accuracy, economy, system, continuity, and speed.

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Notes and References

  1. “Inherited breast cancer is a common genetic disease: 5% of a disease affecting one in ten women over the life span means that roughly 1 in 200 women will develop breast cancer by reason of inherited susceptibility. Therefore, as an inherited trait, breast cancer is one of the most common genetic diseases in the industrialized world.” M.C. King. “Breast Cancer genes: How Many, Where and Who Are they?” Nature Genetics, 2 (1992), pp. 89–90.

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  2. When coming to the issue of “eugenical applications,” she condeded: “Unfortunately there seems to be little hope from the eugenic standpoint of eradication, for usually cancer does not develop in the patient until his children are mature.... It is different with tumors that develop in early childhood such as retinal glioma, which snatch a child from existence at an early age, or plunge him into a world of darkness for a life time. There eugenics has a definite role, and those who have retinal glioma and survived the operation should not pass on the defect to their children....” M.T. Macklin. “The Hereditary Factor in Human Neoplasms,” The Quarterly Review of Biology, VII (1932), pp. 255–281.

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  10. “Pete Little was practically born a geneticist… At Bar Harbor, in a small building whose solid brick walls exclude stray mice, he produces 150,000 mice a year, sells 50,000 to other scientific institutions for research, anatomizes 25,000 to analyse their inherited characteristics, especially their susceptibility to cancer,” Time, March 22, 1937, p. 54.

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  11. National Cancer Advisory Council, Report 1937, reprinted in Journal of National Cancer Institute, 19 (1957).

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  12. Little’s research career deserves an extensive treatment. His role in the development of inbred strains of mice is the topic of K. Rader’s thesis: Making Mice: C. C. Little, the Jackson Laboratory and the Standardization of Mus musculus for Research. Indiana University, forthcoming. On his commitment toward eugenics, see R.G. Clark, The Social Uses of Scientific Knowledge. Eugenics in the Career of C.C. Little (University of Maine, 1956, Master’s dissertation).

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  15. Little, and Tyzzer, “Further Experimental Studies…, p. 396.

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  16. See C.C. Little, “The Heredity of Susceptibility to a Transplantable Sarcoma and (JWB) of the Japanese Waltzing Mouse,” Science, 51 (1920), pp.467–68; C.C. Little and W.B. Johnson. “The Inheritance of Susceptibility to Implants of Splenic Tissue in Mice. I. Japanese Waltzing Mice, Albinos, and Their Fl Generation Hybrids,” Proceedings of the Society for Experimental Biology and Medicine, 19 (1922), pp. 163-167.

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  17. On this dimension, see Clark, chapter 4. “The Scientist as University President.”

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  18. “It seems to me that the efforts toward sterilization which are now fairly widespread have in general a great deal of merit, but they are a rather crude implement. They are so to speak, biological prohibition, instead of biological temperance…. That is curative, not preventive, and sterilization does not reach and probably never can reach the type of individual who is a real menace to civilization, and at the same time one of its law-abiding and useful citizens…. I refer to an individual, normal himself, a good, law-abiding, constructive member of a community, but who carries the hereditary trait in his germ cells of epilepsy or feeble-mindedness or insanity.” C.C. Little, “Unnatural Selection and its Resulting Obligations,” Birth Control Review. 10 (1926), pp. 243–244.

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  19. Ibid. p. 244.

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  20. See Clark, “The Scientist as University President.”

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  21. J. Holsten, The First Fifty Years at the Jackson Laboratory (Bar Harbor: The Jackson Laboratory, 1979).

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  22. On the founding chart, see E.L. Green, “The Jackson Laboratory: A Center for Mammalian Genetics in the United States,” Journal of Heredity, 57 (1966), pp. 3–12.

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  23. For biographical information, See J.J. McCoy, The Cancer Lady: Maud Slye and her Heredity Studies (Nashville, TN: T. Nelson: 1977).

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  24. See C.C. Little “Cancer and Heredity” Science, 42 (1915), pp. 218–219. C.C. Little, “The Inheritance of Cancer,” Science, 42 (1915), pp. 494-95; and M. Slye, “A Reply to Dr. Little,” Science, 42 (1915), pp. 246-248.

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  25. McCoy, The Cancer Lady.

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  26. C.C. Little, “Evidence That Cancer Is Not a Simple Mendelian Recessive,” Journal of Cancer Research, 12 (1928), pp. 30–46.

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  27. Many articles written by Little before World War II include critical views about Slye’s recessive cancer genes. See for example C.C. Little, “The Role of Heredity in Determining the Incidence and Growth of Cancer,”American Journal of Cancer, 15 (1931), pp. 2780–2789; and C.C. Little, “The Present Status of Our Knowledge of Heredity and Cancer,” JAMA. 106 (1936), pp. 2234-2235. For the contribution of Little’s collaborators, see: J.J. Bittner, “The Genetics of Cancer of Mice,” Quarterly Review of Biology, 13 (1938), pp. 51-64. Slye’s reputation was severely damaged by Little’s article. In 1936, she changed her theory, introducing two sets of genetic factors, one set controlling susceptibility to one cancer type, the other set the localization of the tumor. This change has been viewed (Shimkin, 1973) as a closure of the controversy since cancer was turned into a multigenic disease. The move, however, just displaced the arguments. The controversy closed when Slye retired and stopped publishing on cancer.

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  28. M. Slye, “The Relation of Heredity to Cancer,” The Journal of Cancer Research, 12 (1928), pp. 83–133.

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  29. This line of argument was already established when Slye published her first reports. See M. Slye, “The Incidence and Inheritability of Spontaneous Cancer in Mice,” The Journal of Cancer Research, 32 (1915), pp. 159–200.

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  30. See Green, The Jackson Laboratory; andH.C. Morse III, (ed), Origins of Inbred Mice (New York Academic Press, 1978).

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  31. This contrasted with the making of other laboratory animals. See Clause, “The Wistar Rat…”.

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  32. See C.C. Little, “The Present Status of the Cancer Problem,” Annals of Surgery, 93 (1931), pp. 11–15 and C.C. Little, “Some Contributions of the Laboratory Rodents to Our Understanding of Human Biology,” American Naturalist, 73 (1939), pp. 127-138. See also the volume produced collectively by the staff members, G.D. Snell, ed. Biology of the Laboratory Mouse, (New York: MacGraw-Hill, 1941).

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  33. L.C. Strong, “The Establishment of the A Strain of Inbred Mice,” Journal of Heredity, 28 (1937), pp. 21–24.

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  34. R.R. Gates, Eugenics and Heredity, chapter 14. (London Constable, 1929).

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  35. “The fact of inheritance is clear, but the type of inheritance needs further investigation. It does not appear to be simple Mendelian inheritance.” C.C. Little, “The Relations of Genetics to the Problems of Cancer Research.” Harvey Lectures 1921-1922. pp. 65–88. Slye’s arguments are developed in Slye, “The Relation of Heredity to Cancer. “

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  36. “The fact that the tendency to certain forms of cancer is hereditary in mice has been established for some years…. For a time the medical profession was not very willing to accept this fact. Their experience had dealt with human beings, who had bred so slowly and had produced such a small number of progeny from any one mating, and were so difficult to examine and diagnose by the certain method of autopsy, that the details and method of inheritance were none too clear. It was therefore entirely natural that the profession did not at once agree with the conclusions of those engaged in laboratory research…. Too many false hopes have been built up and later destroyed in many investigations on cancer to allow a simple but incorrect genetic interpretation to go unchallenged, especially if it is not well supported by its proponent’s data.” C.C. Little, “Evidence That Cancer is Not a Simple Recessive”, Harvey Lectures 1921–1922.

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  37. D. Kevles, In the Name of Eugenics (Berkeley University of California Press, 1985); K.M. Ludmerer, Genetics and the American Society. (Baltimore: The Johns Hopkins University Press. 1972).

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  38. “There has been such a psychological and sociological maelstrom of ballyhoo and propaganda on economic and allied issues that the country is still spell bound or bilious…. Organized eugenics in the United States is in the doldrums because of several facts. Among these may be cited the following: (1) Lack of confidence on the part of experimental scientists in what has been termed eugenic research; (2) Lack of courage on the part of leaders in biological, sociological and economic fields in facing the conscious control of the quantity and quality of human population; (3) Inability of the average voter at present to see that many if not all our major ills of today are dependant on the fact that we have not used our intellect in the making of men as we have in the production of machinery.” C.C. Little, “Not Dead but Sleeping,” The Journal of Heredity, 24 (1933), pp. 149–150.

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  39. C. Little, “The Present Status of Our Knowledge of Heredity and Cancer,” JAMA., 106 (1936), pp. 2234–2235.

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  40. Staff of Roscoe B. Jackson Memorial Laboratory. “The Existence of Non-chromosomal Influence in the Incidence of Mammary Tumors in Mice.” Science, 78 (1933), pp. 465–466.

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  41. W. Murray and C.C. Little “Extrachromosomal Influence in Relation to the Incidence of Mammary and Non-mammary Tumor in Mice,” American Journal of Cancer, 27 (1936), pp. 516–518.

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  43. W.S. Murray and C.C. Little. “Chromosomal and Extrachromosomal Relation to the Incidence of Mammary Tumors in Mice,” American Journal of Cancer, 37 (1939), pp. 536–552.

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  44. C. Oberling, The Riddle of Cancer, (New Haven: Yale University Press. 1944), p. 162.

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  46. J.J. Bittner, “The Milk Influence of Breast Tumors in Mice,” Science, 95 (1942), pp. 462–463.

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  50. His series rested on three putative mechanisms: inheritance of chromosomes controlling rates of growth in cells, cytoplasmic particles controlling development and differentiation, hormones controlling the development of mammary glands. See Little. “Parental Influence on Cancer,” American Journal of Cancer, 15,1931, p. 97.

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  51. H.B Andervont, “The Milk Influence in the Genesis of Mammary Tumors” in Staff of the National Cancer Institute, A Symposium on Mammary Tumors, Publication of the AAAS, Number 22, ed., F.R. Moulton, 1945.

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  52. The circulation of all Jackson mice showing mammary tumors do not reveal the same pattern. The fact that strain A, which was used in Bittner’s original foster-nursing experiments, did not experience the fate of C3H is suggestive of the contingency of the circulation process.

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  53. J.B. Shimkin, “As Memory Serves: An Informal History of the National Cancer Institute, 1937-1957,” Journal of the National Cancer Institute, 59 (1977), pp. 559–600, see pp. 566-567 on the career of Andervont.

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  54. H.B. Andervont, “Influence of Foster Nursing Upon Incidence of Spontaneous Mammary Tumor Cancer in Resistant and Susceptible Mice,” Journal of the National Cancer Institute, 1 (1940), pp. 147–153.

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  60. Index Medicus shows evidence of this success. From the late 1930s on, the milk agent was the main topic of a dozen articles a year.

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  63. Review in M.B. Shimkin, “Hormones and Mammary Cancer in Mice” in Staff of the National Cancer Institute. A Symposium on Mammary Tumors.

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  65. For instance, the British geneticist L. Penrose concluded one such study: “In view of the work on mice by Bittner, a factor derived from maternal cytoplasm, transmitted by way of milk, colostrom or cytoplasm of the ovum might be a specific cause. If this were so, maternal relatives should be more frequently affected with mammary cancer than the corresponding paternal relatives…. (Our) figures are suggestive though scarcely conclusive of maternal line inheritance.” L.S. Penrose, HJ. Mac Kenzie, and M.N. Kam, “A Genetic Study of Human Mammary Cancer,” British Journal of Cancer, 2 (1948), pp. 168–176.

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  68. The Journal of Heredity then regularly hosted articles on the issue.

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  70. A survey of the ACS journal Cancer News for the years 1947–1955 shows no articles about cancer genetics in humans, although the Committee on Growth established jointly with the National Research Council in 1947 envisioned somework in the field.

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  71. C.C. Little, “Program for Research on the Biology of Human Cancer,” Journal of the National Cancer Institute, 2 (1941), pp. 133–137. The first article on the genetics of human cancer published in the NCI journal came out in 1959. The author was an old-guard figure: M.T. Macklin.

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  73. A sketchy description of the system can be found in Mouse News Letter, 5 (1951), pp. 24–36.

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  76. A general review on mouse mammary tumors written by L. Dmochowski in 1953, mentions dozens of articles published by members of the staff of the Jackson Memorial Laboratory after 1944 and more than 70 during the years 1933–1943.

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  86. Dmochowski’s review of 1953 gives similar weight to the contribution of groups headed by Little (Jackson), Gross (New York), Korteweg (Amsterdam), Bittner (Minneapolis), Heston (NCI), Andervont (NCI), Dmochowski (Leeds).

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© 1999 Springer Science+Business Media Dordrecht

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Gaudilliere, JP. (1999). Circulating Mice and Viruses. In: Fortun, M., Mendelsohn, E. (eds) The Practices of Human Genetics. Sociology of the Sciences, vol 21. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-4718-7_4

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  • DOI: https://doi.org/10.1007/978-94-011-4718-7_4

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