Growth and differentiation of human esophageal carcinoma cell lines - PubMed (original) (raw)
- PMID: 2415247
Growth and differentiation of human esophageal carcinoma cell lines
S P Banks-Schlegel et al. Cancer Res. 1986 Jan.
Abstract
Human esophageal carcinoma cell lines (8 cell lines) differed from their normal counterpart in terms of their morphological appearance, growth properties, and the expression of certain differentiated functions, namely keratin proteins and cross-linked envelopes. In contrast to normal human esophageal keratinocytes, the carcinoma cells were pleomorphic and tended to pile up in an unorganized fashion. When grown under optimal growth conditions the carcinoma cells generally grew to a higher saturation density than their nontransformed counterpart; their generation times were variable. Transformed cells grew better under stringent growth conditions (e.g., decreased serum and no additional growth factors except hydrocortisone) than did nontransformed human esophageal keratinocytes but their growth was still restricted under these conditions. The carcinoma cells retained a requirement for a 3T3 feeder layer when grown at clonal densities (5 X 10(3) cells/60-mm dish) but could be passaged and maintained without a feeder layer if plated at higher than clonal densities (10(5) cells/60-mm dish). All cell lines grew in an anchorage-independent fashion in soft agarose although the colony forming efficiency and size of the colonies varied among the different cell lines. Not all anchorage-independent cell lines were tumorigenic. Tumorigenic potential was greatly augmented by the use of cell lines derived from soft agarose selected clones. Altered expression of keratin proteins and cross-linked envelopes was observed in the carcinoma cell lines and generally reflected those changes seen in primary esophageal carcinomas. In two cell lines (HCE-4 and HCE-6), the synthesis of the Mr 44,000 (analogous to Rheinwald's Mr 40,000 keratin) and 52,000 keratins was suppressed coincident with the appearance of the 67 Kd keratin in tumors derived from these cell lines. These keratin patterns were once again reversed in cell lines recultured from these tumors, suggesting that the expression of these specific keratins is subject to extrinsic growth regulation. Another feature of terminal differentiation in keratinocytes, cross-linked envelope formation, was found to be significantly altered (reduced) in most but not all human esophageal carcinoma cell lines.
Similar articles
- Aberrant expression of keratin proteins and cross-linked envelopes in human esophageal carcinomas.
Banks-Schlegel SP, Harris CC. Banks-Schlegel SP, et al. Cancer Res. 1984 Mar;44(3):1153-7. Cancer Res. 1984. PMID: 6198080 - Environmental induction of differentiation-specific keratins in malignant mouse keratinocyte lines.
Breitkreutz D, Hornung J, Pöhlmann J, Brown-Bierman L, Bohnert A, Bowden PE, Fusenig NE. Breitkreutz D, et al. Eur J Cell Biol. 1986 Dec;42(2):255-67. Eur J Cell Biol. 1986. PMID: 2434329 - Rat esophageal and epidermal keratinocytes: intrinsic differences in culture and derivation of continuous lines.
Heimann R, Rice RH. Heimann R, et al. J Cell Physiol. 1983 Dec;117(3):362-7. doi: 10.1002/jcp.1041170311. J Cell Physiol. 1983. PMID: 6197421 - Human squamous cell carcinoma in culture: a defect in terminal differentiation and its relation to malignancy.
Rheinwald JG. Rheinwald JG. Natl Cancer Inst Monogr. 1982;60:133-8. Natl Cancer Inst Monogr. 1982. PMID: 6981772 - Differentiation, cancer, and anticancer activity.
Tzen CY, Estervig DN, Minoo P, Filipak M, Maercklein PB, Hoerl BJ, Scott RE. Tzen CY, et al. Biochem Cell Biol. 1988 Jun;66(6):478-89. doi: 10.1139/o88-060. Biochem Cell Biol. 1988. PMID: 3048326 Review.
Cited by
- Ranking candidate genes of esophageal squamous cell carcinomas based on differentially expressed genes and the topological properties of the co-expression network.
Shen Y, Tantai J, Zhao H. Shen Y, et al. Eur J Med Res. 2014 Oct 29;19(1):52. doi: 10.1186/s40001-014-0052-x. Eur J Med Res. 2014. PMID: 25358439 Free PMC article. Retracted. - Tumor-Derived CCL5 Recruits Cancer-Associated Fibroblasts and Promotes Tumor Cell Proliferation in Esophageal Squamous Cell Carcinoma.
Dunbar KJ, Karakasheva TA, Tang Q, Efe G, Lin EW, Harris M, Sahu V, Sachdeva UM, Hu J, Klein-Szanto AJ, Henick B, Diehl JA, Nakagawa H, Rustgi AK. Dunbar KJ, et al. Mol Cancer Res. 2023 Jul 5;21(7):741-752. doi: 10.1158/1541-7786.MCR-22-0872. Mol Cancer Res. 2023. PMID: 37027010 Free PMC article. - Frequent mutation of the p53 gene in human esophageal cancer.
Hollstein MC, Metcalf RA, Welsh JA, Montesano R, Harris CC. Hollstein MC, et al. Proc Natl Acad Sci U S A. 1990 Dec;87(24):9958-61. doi: 10.1073/pnas.87.24.9958. Proc Natl Acad Sci U S A. 1990. PMID: 2263646 Free PMC article. - Altered expression of the cyclin D1 and retinoblastoma genes in human esophageal cancer.
Jiang W, Zhang YJ, Kahn SM, Hollstein MC, Santella RM, Lu SH, Harris CC, Montesano R, Weinstein IB. Jiang W, et al. Proc Natl Acad Sci U S A. 1993 Oct 1;90(19):9026-30. doi: 10.1073/pnas.90.19.9026. Proc Natl Acad Sci U S A. 1993. PMID: 8415648 Free PMC article. - Molecular characterization and expression of the stratification-related cytokeratins 4 and 15.
Leube RE, Bader BL, Bosch FX, Zimbelmann R, Achtstaetter T, Franke WW. Leube RE, et al. J Cell Biol. 1988 Apr;106(4):1249-61. doi: 10.1083/jcb.106.4.1249. J Cell Biol. 1988. PMID: 2452170 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Medical
Research Materials