Naturally occurring and artificially induced tumor-like formations in marine invertebrates: A search for permanent cell lines

Journal of Experimental Marine Biology and Ecology

Volumn 407, Issue 2, 2011, Pages 241-249

  Odintsova, Nelly A ^a,b   Usheva, Ludmila N ^a   Yakovlev, Konstantin V ^a   Kiselev, Konstantin V ^c  

^a INSTITUTE OF MARINE BIOLOGY   (Russian Federation)

^b FAR EASTERN FEDERAL UNIVERSITY   (Russian Federation)

^c INSTITUTE OF BIOLOGY AND SOIL SCIENCE   (Russian Federation)

Author keywords

Bivalve mollusc; Cell line; Mitotic activity; Neoplasia; Sea urchin; Tumor like formation

Indexed keywords

BIOTECHNOLOGY; BIVALVE; CELL ORGANELLE; DEVELOPMENTAL BIOLOGY; EMBRYO; ESTIMATION METHOD; GENE EXPRESSION; GENETICALLY MODIFIED ORGANISM; GROWTH; INVERTEBRATE; LABORATORY METHOD; MARINE ENVIRONMENT; NUMERICAL MODEL; TUMOR; YEAST;

PACIFIC OCEAN; SEA OF JAPAN;

BIVALVIA; ECHINOIDEA; INVERTEBRATA; MOLLUSCA; MYTILUS; PECTEN;

EID: 80052448705     PISSN: 00220981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jembe.2011.06.020     Document Type: Article

References (64)

1. Barber B. Neoplastic diseases of commercially important marine bivalves. Aquat. Living Resour. 2004, 17(4):449-466.
2. Barry M.M., Yevich P.P., Thayer N.H. Atypical hyperplasia in the soft-shell clam Mya arenaria. J. Invertebr. Pathol. 1971, 17(1):17-27.
3. Boveri T. Zur frage der entstehung maligner tumoren (Jena: Gustav Fischer) (English translation). The Origin of Malignant Tumors, Marcella Boveri (translator) 1914, Baltimore: Williams and Wilkins; 1929.
4. Bulgakov V.P., Odintsova N.A., Plotnikov S.V., Kiselev K.V., Zacharov E.V., Zhuravlev Yu.N. Gal4 gene-dependent alterations of embryo development and cell growth in a primary culture of the sea urchins. Mar. Biotechnol. 2002, 4(5):480-486.
5. Bulgakov V.P., Kiselev K.V., Yakovlev K.V., Zhuravlev Yu.N., Gontcharov A.A., Odintsova N.A. Agrobacterium-mediated transformation of sea urchin embryos. Biotechnol. J. 2006, 1(4):454-461.
6. Chelomin V.P., Zakhartsev M.V., Kurilenko A.V., Belcheva N.N. An in vitro study of the effect of reactive oxygen species on subcellular distribution of deposited cadmium in digestive gland of mussel Crenomytilus grayanus. Aquat. Toxicol. 2005, 73(2):181-189.
7. Chen S.N., Wen C.M. Establishment of cell lines derived from oyster, Crassostrea gigas Thunberg and hard clam Meretrix lusoria Roding. Meth. Cell Science 1999, 21(2):183-192.
8. Cornet M. Primary mantle tissue culture from the bivalve mollusc Mytilus galloprovincialis: investigations on the growth promoting activity of the serum used for medium supplementation. J. Biotechnol. 2006, 123(1):78-84.
9. Claydon K., Owens L. Attempts at immortalization of crustacean primary cell cultures using human cancer genes. In Vitro Cell. Dev. Biol.-Animal 2008, 44(10):451-457.
10. Desvoigne D.M., Mix M.C., Pauley G.B. A papillomalike growth on the siphon of the horse clam Tresus nuttalli. J. Invertebr. Pathol. 1970, 15(2):262-267.
11. Dix T.G. Two mesenchymal tumors in a pearl oyster Pinctada margaritifera. J. Invertebr. Pathol. 1972, 20(3):317-320.
12. Ellis L.L., Bishop S.H. Isolation of cell lines with limited growth potential from marine bivalves. Invertebrate Cell System Applications 1989, V. 2:243-251. CRC Press, Boca Raton, FL.
13. Ellis L.L. Electroporation of oyster cells. In vitro Cell Dev. Biol.-Animal 1991, 27(42A).
14. Elston R.A., Kent M.L., Drum A.S. Transmission of hemic neoplasia in the bay mussel, Mytilus edulis, using whole cells and cell homogenate. Dev. Comp. Immunol. 1988, 12(4):719-727.
15. Farley C.A. Sarcomatid proliferative disease in a wild population of blue mussels (Mytilus edulis). J. Natl. Cancer Inst. 1969, 43(2):509-516.
16. Filippini F., Rossi V., Marin O., Trovato M., Costantino P., Downey P.M., Lo Schiavo F., Terzi M. A plant oncogene as a phosphatase. Nature 1996, 379(6565):499-500.
17. Flandre O. The culture of molluscan cells. Invertebrate Tissue Culture 1974, V. 1:361-363. Acad. Press, NY.
18. Jones K.H., Senft J.A. An improved method to determine cell viability by simultaneous staining with fluorescein diacetate-propidium iodide. J. Histochem. Cytochem. 1985, 33(1):77-79.
19. Gardner G.R., Pruell R.J., Malcolm A.R. Chemical induction of tumors in oysters by a mixture of aromatic and chlorinated hydrocarbons, amines and metals. Mar. Environ. Res. 1992, 34(1-4):59-63.
20. Galimany E., Sunila I. Several cases of disseminated neoplasia in mussels Mytilus edulis (L.) in Western Long Island Sound. J. Shellfish. Res. 2008, 27(5):1201-1207.
21. Hansen E.L. Initiating a cell line from embryos of the snail Biomphalaria glabrata. Tissue Cult. Assoc. Manual. 1979, 5(25):1009-1014.
22. Hanselmann R., Smolowitz R., Gibson D. Identification of proliferating cells in hard clams. Biol. Bull. 2000, 199(2):199-200.
23. Jiravanichpaisal P., Soderhall K., Soderhall I. Characterization of white spot syndrome virus replication in in vitro-cultured haematopoietic stem cells of freshwater crayfish Pacifastacus leniusculus. J. Gen. Virol. 2006, 87(4):847-854.
24. Kleinschuster S.J., Parent J., Walker C.W., Farley C.A. A cardiac cell line from Mya arenaria (Linnaeus, 1759). J. Shellfish. Res. 1996, 15(3):695-707.
25. Khudoley V.V., Syrenko O.A. Tumor induction by N-nitroso compounds in bivalve mollusks Unio pictorum. Cancer Lett. 1978, 4(6):349-354.
26. Lauckner G. Diseases of Mollusca: Bivalvia. Abnormalities. Neoplasia. Diseases of marine animals, Vol. II 1983, 848-963. Biologische Anstalt Helgoland, Hamburg. O. Kinne (Ed.).
27. Le Pennec G., Le Pennec M. Acinar primary cell culture from the digestive gland of Pecten maximus (L.): an original model for ecotoxicological purposes. J. Exp. Mar. Biol. Ecol. 2001, 259(2):171-187.
28. Lillie R.D. Histopathologic Technic and Practical Histochemistry 1965, Acad. Press, McGraw-Hill, NY, pp. 456-516.
29. Lin Y.-S., Green M.R. Mechanism of action of an acidic transcriptional activator in vitro. Cell 1991, 64(5):971-981.
30. Ma J., Ptashne M. Deletion analysis of GAL4 defines two transcriptional activating segments. Cell 1987, 48(5):847-853.
31. Maramorosch K. Invertebrate Tissue Culture: Research Applications 1976, Acad. Press, NY.
32. Marigómez I., Lekube X., Cancio I. Immunochemical localisation of proliferating cells in mussel digestive gland tissue. Histochem. J. 1999, 31(12):781-788.
33. McLaughlin S.M., Farley C.A., Hetrick F.M. Transmission studies of sarcoma in the soft-shell clam, Mya arenaria. In Vitro 1992, 6(4):367-370.
34. Mix M.C. A general model for leukocyte cell renewal in bivalve mollusks. Mar. Fish Bull. 1976, 38(10):37-41.
35. Mottin E., Caplat C., Mahaut M., Costil K., Barillier D., Lebel J., Serpentini A. Effect of in vitro exposure to zink on immunological parameters of haemocytes from the marine gastropod Haliotis tuberculata. Fish Shellfish Immun. 2010, 29(5):846-853.
36. Odintsova N.A., Dolmatov I.Yu., Mashanov V.S. Regenerating holothurian tissues as a source of cells for long-term cell cultures. Mar. Biol. 2005, 146(5):915-921.
37. Odintsova N.A., Ermak A.V., Tsal L.G. Substrate selection for long-term cultivation of marine invertebrate cells. Comp. Bioch. Physiol. 1994, 107A(4):613-619.
38. Odintsova N.A., Kiselev K.V., Bulgakov V.P., Koltsova E.A., Yakovlev K.V. Influence of the activator of transcription gal4 on growth and development of embryos and embryonic cells in primary cultures of sand dollar. Russ. J. Dev. Biol. 2003, 34(4):217-222.
39. Pauley G.B. A butter clam (Saxidomus giganteus) with a polypoid-tumor on the foot. J. Invertebr. Pathol. 1967, 9(5):576-579.
40. Pauley G.B., Sayce C.S. An internal fibrous tumor in a Pacific oyster Crassostrea gigas. J. Invertebr. Pathol. 1968, 10(1):1-8.
41. Pauley G.B. A critical review of neoplasia and tumor-like lesions in molluscs: neoplasms and related disorders in invertebrates and lower vertebrate animals. Natl. Cancer Inst. Monogr. 1969, 31:509-539.
42. Pekkarinen M. Neoplastic diseases in the Baltic Macoma baltica (Bivalvia) off the Finnish coast. J. Invertebr. Pathol. 1993, 61(2):138-146.
43. Perkins F.O., Menzel R.W. Maintenance of oyster cells in vitro. Nature 1964, 204(4963):1106-1107.
44. Peters E.C. Recent investigations on the disseminated sarcomas of marine bivalve mollusks. Am. Fish Soc. Publ. 1988, 18(1):74-92.
45. Peters E.C. Comparative histopathology of gonadal neoplasms in marine bivalve molluscs. Dis. Aquat. Org. 1994, 20(1):59-76.
46. Reno P.W., House M., Illingworth E. Flow cytometric and chromosome analysis of soft-shell clams Mya arenaria with disseminated neoplasia. J. Invertebr. Pathol. 1994, 64(2):163-172.
47. Rinkevich B. Marine invertebrate cell cultures: new millennium trends. Mar. Biotechnol. 2005, 7(5):429-439.
48. Schäfer S., Köhler A. Gonadal lesions of female sea urchin (Psammechinus miliaris) after exposure to the polycyclic aromatic hydrocarbon phenanthrene. Mar. Environ. Res. 2009, 68(3):128-136.
49. Sokal R.R., Rohlf F.J. Biometry 1981, W. H, Freeman, San Francisco. 2nd ed.
50. Sparks A.K. Tumors and tumorlike conditions in invertebrates. Invertebrate pathology: noncommunicable diseases 1972, 271-371. Acad. Press, New York, London.
51. Sparks A.K. Tumors and tumor-like lesions in invertebrates. Synopsis of Invertebrate Pathology, Elsevier Science 1985, 91-132. Amsterdam/Oxford, New York.
52. Sunila I. Respiration of sarcoma cells from the soft-shell clam Mya arenaria L. under various conditions. J. Exp. Mar. Biol. Ecol. 1991, 150(1):19-29.
53. Sunila I. Serum-cell interactions in transmission of sarcoma in the soft shell clam Mya arenaria. Comp. Biochem. Phys. 1992, 102A(4):727-730.
54. Takahashi K., Yamanaka S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell 2006, 126(4):663-676.
55. Toullec J.Y. Crustacean primary cell culture: a technical approach. Meth. Cell Sci. 1999, 21(4):193-198.
56. Tripp M.R. Cellular responces of molluscs. Ann. NY Acad. Sci. 1963, 113:467-474.
57. Usheva L.N., Odintsova N.A. Mesenchymal tumor in the mantle of the mussel Modiolus difficilis from Amursky Bay in the Sea of Japan. Dis. Aquat. Org. 1997, 29(2):121-126.
58. Usheva L.N., Frolova L.T. Neoplasia in the connective tissue of the mussel Mytilus trossulus from polluted areas of Nakhodka Bay in the Sea of Japan. Russ. J. Dev. Biol. 2000, 31(1):63-70.
59. Van Beneden R.J. Molecular analysis of bivalve tumors: models for environmental-genetic interactions. Environ. Health Perspect. 1994, 102(12):81-83.
60. Vaschenko M.A., Zhadan P.M., Latypova E.V. Long-term changes in the state of gonads in sea urchins Strongylocentrotus intermedius from Amur Bay, the Sea of Japan. Russ. J. Ecology 2001, 32(5):358-364.
61. Villalba A., Azevedo C., Rodríques C. Occurrence of multiple hyperplastic growths on the gills of Pacific oyster, Crassostrea gigas, and their relationship with associated pathologic conditions. J. Invertebr. Pathol. 1993, 62(2):296-302.
62. Walker C., Böttger S.A., Mulkern J., Jerszyk E., Litvaitis M., Lesser M. Mass culture and characterization of tumor cells from a naturally occurring invertebrate cancer model: applications for human and animal disease and environmental health. Biol. Bull. 2009, 216(1):23-39.
63. Yuh C.-H., Bolouri H., Davidson E.H. Genomic cis-regulatory logic: experimental and computational analysis of a sea urchin gene. Science 1998, 279(5358):1896-1902.
64. Zaldibar B., Cancio I., Marigómez I. Circatidal variation in epithelial cell proliferation in the mussel digestive gland and stomach. Cell Tissue Res. 2004, 318(2):395-402.