Skip to main content
Log in

A novel assay for the quantification of invasion from raft cultures of lung carcinomas

  • Published:
Clinical & Experimental Metastasis Aims and scope Submit manuscript

Abstract

Assays that conveniently quantify invasion of carcinoma cells in vitro have generally measured the passage of dissociated cells into a matrix. Although these assays have been helpful in identifying relative differences between different carcinoma cell lines or types, the requirement for dissociation overlooks the possible modulation of invasion by cell–cell interactions among carcinoma cells. Described here is a novel assay that quantifies invasion of a matrix placed above intact, multilayered raft cultures of lung carcinoma cell lines A549 and H520. The assay was performed by placing a porous membrane coated with matrix at the air interface of the raft cultures for varying lengths of time, after which the cells invading the matrix were enumerated. The numbers of cells invading increased in a relatively linear fashion from 24 to 72 h, and the absolute numbers within each cell line were reproducible with multiple sets of raft cultures prepared at different times. It was also found that this assay could quantify differences in invasion caused by changes in matrix composition. It is concluded that this assay can reproducibly quantify carcinoma cell invasion from three dimensional raft cultures.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Kramer RH, Nicolson GL. Interactions of tumor cells vascular endothelial cell monolayers: a model for metastatic invasion. Proc Natl Acad Sci 1979; 76(11): 5704–8.

    CAS  PubMed  Google Scholar 

  2. Zamora PO, Danielson KG, Hosick HL. Invasion of endothelial cell monolayers on collagen gels by cells from mammary tumor spheroids. Cancer Res 1980; 40(12): 4631–9.

    CAS  PubMed  Google Scholar 

  3. Starkey JR, Hosick HL, Stanford DR et al. Interaction of metastatic tumor cells with bovine lens capsule basement membrane. Cancer Res 1984; 4(44): 1585–94.

    Google Scholar 

  4. Albini A, Iwamoto Y, Kleinman HK et al. A rapid in vitro assay for quantitating the invasive potential of tumor cells. Cancer Res 1987;47(12): 3239–45.

    CAS  PubMed  Google Scholar 

  5. Hendrix MJ, Seftor EA, Seftor RE et al. A simple quantitative assay for studying the invasive potential of high and low human metastatic variants. Cancer Lett 1987; 381(1-2): 137–47.

    Google Scholar 

  6. Gohla A, Eckert K, Maurer HR. A rapid and sensitive fluorometric screening assay using YO-PRO-1 to quantify tumour cell invasion through Matrigel. Clin Exp Metast 1996; 14: 451–8.

    Article  CAS  Google Scholar 

  7. Platet N, Garcia M. A new bioassay using transient transfection for invasion-related gene analysis. Invasion Metast 1999; 18: 198–208.

    CAS  Google Scholar 

  8. Benbow U, Orndorff KA, Brinckerhoff C et al. Confocal assay for invasion: Use of propidium indide fluorescence and laser reflectance to quantify the rate of migration of cells throught a matrix. Cytometry 2000; 40: 253–9.

    Article  CAS  PubMed  Google Scholar 

  9. Yoh H, Takeo S, Aikou T. A novel fluorometric invasion assay for quantitative determination of tumor cell invasion. Lab Invest 2002; 82(1): 109–111.

    PubMed  Google Scholar 

  10. Nakayama Y, Naito S, Ryuto M et al. An in vitro invasion model for human renal cell carcinoma cell lines mimicking their metastatic abilities. Clin Exp Metast 1996; 14: 466–74.

    Article  CAS  Google Scholar 

  11. Yamada S, Toda S, Shin T et al. Effects of stromal fibroblasts and fat cells and an environmental factor air exposure on invasion of laryngeal carcinoma (HEp-2) cells in a collagen gel invasion assay system. Arch Otolaryngol Head Neck Surg 1999; 125: 424–31.

    CAS  PubMed  Google Scholar 

  12. Alroy J, Pauli BU, Weinstein RS. Correlations between numbers of desmosomes and aggressiveness of transitional cell carcinoma in human urinary bladder. Cancer 1981; 47: 104–12.

    CAS  PubMed  Google Scholar 

  13. McDonagh D, Vollmer RT, Shelburne JD. Intercellular junctions and tumor behavior in lung cancer. Mod Pathol 1991; 4(4): 436–40.

    CAS  PubMed  Google Scholar 

  14. Green KJ, Stappenbeck TS, Noguchi S et al. Desmoplakin expression and distribution in cultured rat bladder epithelial cells of varying tumorigenic potential. Exp Cell Res 1991; 193: 134–43.

    Article  CAS  PubMed  Google Scholar 

  15. Shinohara M, Hiraki A, Ikebe T et al. Immunohistochemical study of desmosomes in oral squamous cell carcinoma: correlation with cytokeratin and eol-cadherin staining, and with tumor behavior. J Path 1998; 184: 369–81.

    CAS  PubMed  Google Scholar 

  16. Krunic A, Garrod DR, Madani S et al. Immunohistochemical staining for desmogleins 1 and 2 in keratinocytic neoplasms with squamous phenotype: Actinic keratosis, keratoacanthoma and squamous cell carcinoma of the skin. Br J Cancer 1998; 77(8): 1275–9.

    CAS  PubMed  Google Scholar 

  17. Wilson JL, Dollard SC, Chow LT et al. Epithelial-specific gene expression during differentiation of stratified primary human keratinocyte cultures. Cell Growth Diff 1992; 3(8): 471–83.

    CAS  PubMed  Google Scholar 

  18. Dollard SC, Wilson JL, Demeter LMet al. Production of human papillomavirus and modulation of the infectious program in epithelial raft cultures. Genes Develop 1992; 6(7): 1131–42.

    CAS  PubMed  Google Scholar 

  19. Parnigotto PP, Bassani V, Gottardo A et al. Growth, morphology, morphometry and keratin patterns of bovine corneal epithelial cells cultured in vitro. Anatom Anzeiger 1996; 178(6): 545–51.

    CAS  Google Scholar 

  20. Serewko MM, Popa C, Dahler AL et al. Alterations in gene expression and activity during squamous cell carcinoma development. Cancer Res 2002; 62(13): 3759–65.

    CAS  PubMed  Google Scholar 

  21. Hanzawa M, Shindoh M, Higashino F et al. Hepatocyte growth factor upregulates E1AF that induces oral squamous cell carcinoma cell invasion by activating matrix metalloproteinase genes. Carcinogenesis 2000; 21(6): 1079–85.

    Article  CAS  PubMed  Google Scholar 

  22. Dicker AJ, Serewko MM, Dahler AL et al. Functional characterization of cultured cells derived from an intraepidermal carcinoma of the skin (IEC-1). Exp Cell Res 2000; 258(2): 352–60.

    Article  CAS  PubMed  Google Scholar 

  23. Behbakht K, DeGeest K, Turyk ME et al. All-trans-retinoic acid inhibits the proliferation of cell lines derived from human cervical neoplasia. Gynecol Oncol 1996; 61(1): 31–9.

    Article  CAS  PubMed  Google Scholar 

  24. Pantel K, Passlick B, Vogt J et al. Reduced expression of plakoglobin indicates an unfavorable prognosis in subsets of patients with nonsmall cell lung cancer. J Clin Oncol 1998; 16: 1407–13.

    Google Scholar 

  25. Young GD, Winokur TS, Cerfolio RJ et al. Differential expression and biodistribution of cytokeratin 18 and desmoplakins in non-small cell lung carcinoma subtypes. Lung Cancer 2002; 36(2): 133–41.

    Article  PubMed  Google Scholar 

  26. Mukai M, Shinkai K, Yoshioka K et al. Mechanism of tumor cell invasion studied by a culture model-modification of invasiveness by host mediators. Human Cell 1993; 6: 194–8.

    CAS  PubMed  Google Scholar 

  27. O-charoenrat P, Rhys-Evans P, Court WJ et al. Differential modulation of proliferation, matrix metalloproteinase expression and invasion of human head and neck squamous carcinoma cells by c-erbB ligands. Clin Exp Metast 1999; 17: 631–9.

    Article  CAS  Google Scholar 

  28. Lu Z, Jiang G, Blume-Jensen P et al. Epidermal growth factor-induced tumor cell invasion and metastasis initiated by dephosphorylation and downregulation of focal adhesion kinase. Mol Cell Biol 2001; 21: 4016–31.

    CAS  PubMed  Google Scholar 

  29. Ueda M, Fujii H, Yoshizawa K et al. Effects of EGF and TGF-alpha on invasion and proteinase expression of uterine cervical adenocarcinoma OMC-4 cells. Invas Metast 1998-1999; 18: 176–83.

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Robert I. Garver Jr..

Rights and permissions

Reprints and permissions

About this article

Cite this article

Okoh, V., Young, G.D., Winokur, T.S. et al. A novel assay for the quantification of invasion from raft cultures of lung carcinomas. Clin Exp Metastasis 21, 1–6 (2004). https://doi.org/10.1023/B:CLIN.0000017159.12425.c9

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/B:CLIN.0000017159.12425.c9

Navigation