The effect s of growth factors and calcium concentrations present in different culture media on induction of terminal differentiation were investigated for four different epidermoid carcinoma cell lines, Hela, KB, A431, and SCC - 25, and their responses determined relative to those elicited by normal human keratinocytes subjected to these culture conditions. Differentiation status was determined cyto-chemically by a validated keratin protein staining method, and by autoradiographic analyses. Growth and differentiation promoting factors that influence d the direction of integrated control of growth and differentiation in normal human keratinocytes were found to be effective for some cell lines but not others. The factors examined were 1) high density arrest in serum-free and serum-containing media, 2) media shifts from high density culture in serum-containing media to low density growth factor-depleted or supplemented serum-free medium, and 3) the concentration of calcium in the media. The extent and degree of differentiation achieved varied among different cell lines depend on the presence or absence of serum, EGF and insulin protein growth fac tors. Certain growth media appear to sponsor keratin protein , cyto-chemically- detected differentiation , and evidence of quantal mitotic division in low density HeLa cell and SCC25 cell cultures. Epidermoid carcinoma cell lines retain limited capacity to commit to early stages of cell differentiation.
Weinberg, R.A. (2007) The Biology of Cancer Garland Science. Taylor & Francis Group, LLC, New York, NY.
Steinberg, M.L. and Defendi, V. (1979) Altered Pattern of Growth and Differentiation in Human Keratinocytes Infected by Simian Virus 40. Proceedings of the National Academy of Sciences of the United States of America, 76, 801-805. http://dx.doi.org/10.1073/pnas.76.2.801
Ayoub, P. and Shklar, G. (1963) A Modification of the Mallory Connective Tissue Stain as a Stain for Keratin. Oral Surgery, 16, 581. http://dx.doi.org/10.1016/0030-4220(63)90148-8
Scott, R.E., Wilke, M.S., Wille Jr., J.J., Pittelkow, M.R., Hsu, B.M. and Kasperbauer, J.L. (1988) Human Squamous Carcinoma Cells Express Complex Defects in the Control of Proliferation and Differentiation. The American Journal of Pathology, 133, 374-380.
Fusenig, N.E., Breitkreutz, D., Dzarlieva, R.T., Bukamp, P., Bohnert, A. and Tilgen, W. (1983) Growth and Differentiation Characteristics of Transformed Keratinocytes from Mouse and Human Skin in Vitro and in Vivo. Journal of Investigative Dermatology, 81, 168s-175s. http://dx.doi.org/10.1111/1523-1747.ep12541032
Wille, J.J. and Scott, R.E. (1986) Suppression of Tumorigenicity in Cell Cycle-Dependent Control of Cellular Differentiation and Proliferation. International Journal of Cancer, 37, 875-881. http://dx.doi.org/10.1002/ijc.2910370613
Pittelkow, M.R., Wille, J.J. and Scott, R.E. (1986) Two Functionally Distinct Classes of Growth Arrest States in Human Prokeratinocytes That Regulate Clonogenic Potential. Journal of Investigative Dermatology, 86, 410-417. http://dx.doi.org/10.1111/1523-1747.ep12285684
Wille, J.J., Pittelkow, M.R., Shipley, G.D. and Scott, R.E. (1984) Integrated Control of Growth and Differentiation of Normal Human Prokeratinocytes Cultured in Serum-Free Medium: Clonal Analyses, Growth Kinetics, and Cell Cycle Studies. Journal of Cellular Physiology, 121, 31-44. http://dx.doi.org/10.1002/jcp.1041210106
Wille, J.J., Burdge, J.J. and Pittelkow, M.R. (2011) Rapid Healing of Chronic Venous Stasis Leg Ulcers Treated by the Application of a Novel Serum-Free Cultured Autologous Epidermis. Wound Repair and Regeneration, 19, 464-474. http://dx.doi.org/10.1111/j.1524-475X.2011.00702.x
Dean, P.N. and Jett, J.H. (1974) Mathematical Analysis of DNA Distributions Derived from Flow Microfluorimetry. The Journal of Cell Biology, 60, 523-527. http://dx.doi.org/10.1083/jcb.60.2.523
Rudden, R. (1981) Cellular Differentiation and Cancer. In: Rudden, R., Ed., Cancer Biology, Oxford University Press, New York, 99-119.
Chinkers, M., McKanna, J.A. and Cohen, S. (1981) Rapid Rounding of Human Epidermoid Carcinoma Cells A431 Induced by Epidermal Growth Factor. The Journal of Cell Biology, 88, 422-429. http://dx.doi.org/10.1083/jcb.88.2.422
Lifschitz, A., Lazar, C.S., Buss, J.E. and Gill, G.N. (1983) Analysis of Morphology and Receptor Metabolism in Clonal Variant A431 Cells with Differing Growth Responses to Epidermal Growth Factor. Journal of Cellular Physiology, 115, 235-242. http://dx.doi.org/10.1002/jcp.1041150304
Scott, R.E., Hoerl, B.J., Wille, J.J., Florine, D.L., Krawisz, B.R. and Yun, K. (1982) Coupling of Proadipocyte Growth Arrest and Differentiation. II. A Cell Cycle Model for the Physiological Control of Cell Proliferation. The Journal of Cell Biology, 94, 400-405. http://dx.doi.org/10.1083/jcb.94.2.400
Scott, R.E., Florine, D.L., Wille, J.J. and Yun, K. (1982) Coupling of Growth Arrest and Differentiation at a Distinct State in the G1 Phase of the Cell Cycle: GD. Proceedings of the National Academy of Sciences of the United States of America, 79, 845-849. http://dx.doi.org/10.1073/pnas.79.3.845
Wilke, M., Hsu, B., Wille Jr., J.J., Pittelkow, M.R. and Scott, R.E. (1988) Biologic Mechanisms for the Regulation of Normal Human Keratinocyte Proliferation and Differentiation. The American Journal of Pathology, 131, 171-181.
Marks, P.A. and Rifkin, R.A. (1978) Erythroleukemic Differentiation. Annual Review of Biochemistry, 47, 419. http://dx.doi.org/10.1146/annurev.bi.47.070178.002223
Lotan, R., Neumann, G. and Lotan, D. (1981) Characterization of Retinoic Acid-Induced Alterations in the Proliferation and Differentiation of a Murine and a Human Melanoma Cell lIne in Culture. Modulation of Cellular Interactions by Vitamin A and Derivatives (Retinoids), Annals of the New York Academy of Sciences, 359, 150-170. http://dx.doi.org/10.1111/j.1749-6632.1981.tb12744.x
Wille, J.J. and Chopra, D. (1988) Reversal by Retinoids of Keratinization Induced by Benzo[α]pyrene in Normal Hamster Tracheal Explants: Comparison with the Assay Involving Organ Cultures of Tracheas from Vitamin A-Deficient Hamsters. Cancer Letters, 40, 235-246. http://dx.doi.org/10.1016/0304-3835(88)90082-1
Verma, A.K., Shapas, B.G., Rice, H.M. and Bojtwell, R.K. (1979) Correlation of the Inhibition by Retinoids of Tumor Promoter-Induced Mouse Epidermal Ornithine Decarboxylase Activity and of Skin Tumor Promotion. Cancer Research, 39, 419-425.
Holzer, H., Schultheiss, T., Dilullo, C., Choi, J., Costa, M., Lu, M. and Holtzer, S. (1990) Autonomous Expression of the Differentiation Programs of Cells in the Cardiac and Skeletal Myogenic Lineages. Annals of the New York Academy of Sciences, 599, 158-169. http://dx.doi.org/10.1111/j.1749-6632.1990.tb42374.x
Pierce, G.B. (1970) Differentiation of Normal and Malignant Cells. Federation of American Societies for Experimental Biology, 29, 1248-1254.
Pierce, G.B., Aguilar, D., Hood, G. and Wells, R.S. (1984) Trophectoderm in Control of Murine Embryonal Carcinoma. Cancer Research, 44, 3987-3996.
Pierce, G.B. and Wallace, C. (1971) Differentiation of Malignant to Benign Cells. Cancer Research, 31, 127-134.