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Contaminating cells alter gene signatures in whole organ versus laser capture microdissected tumors: a comparison of experimental breast cancers and their lymph node metastases

Clinical & Experimental Metastasis volume 25, pages 81–88 (2008)Cite this article

Abstract

Genome-wide expression profiling has expedited our molecular understanding of the different subtypes of breast cancers, as well as defined the differences among genes expressed in primary tumors and their metastases. Laser-capture microdissection (LCM) coupled to gene expression analysis allows us to understand how specific cell types contribute to the total cancer gene expression signature. Expression profiling was used to define genes that contribute to breast cancer spread into and/or growth within draining lymph nodes (LN). Whole tumor xenografts and their matched whole LN metastases were compared to LCM captured cancer cells from the same tumors and matched LN metastases. One-thousand nine-hundred thirty genes were identified by the whole organ method alone, and 1,281 genes by the LCM method alone. However, less than 1% (30 genes) of genes that changed between tumors and LN metastases were common to both methods. Several of these genes have previously been implicated in cancer aggressiveness. Our data show that whole-organ and LCM based gene expression profiling yield distinctly different lists of metastasis-promoting genes. Contamination of the tumor cells, and cross reactivity of mouse RNA to human-specific chips may explain these differences, and suggests that LCM-derived data may be more accurate.

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Abbreviations

CK18:

Cytokeratin 18

ER:

Estrogen receptor

H & E:

Hematoxylin and eosin

LCM:

Laser-capture microdissection

LN:

Lymph node

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Acknowledgements

These studies were supported by a Department of Defense Predoctoral Breast Cancer Training Grant BC050889 to JCH; and by NIH Grant CA26869, the National Foundation for Cancer Research, the Avon Foundation and the Breast Cancer Research Foundation grants to KBH. The authors would like to thank the UCHSC Laser-Capture and Microarray Core Laboratories.

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Affiliations

  1. Division of Endocrinology, Department of Medicine, University of Colorado Health Sciences Center, MS 8106, RC-1 South, 12801 E. 17th Ave, Room 7402G, PO Box 6511, Aurora, CO, 80045, USA

    Joshua Chuck Harrell, Wendy W. Dye, Djuana M. E. Harvell, Carol A. Sartorius & Kathryn B. Horwitz

  2. Department of Pathology, University of Colorado Health Sciences Center, Aurora, CO, USA

    Kathryn B. Horwitz

  3. Program in Reproductive Sciences, University of Colorado Health Sciences Center, Aurora, CO, USA

    Joshua Chuck Harrell & Kathryn B. Horwitz

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  1. Joshua Chuck Harrell
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  2. Wendy W. Dye
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  3. Djuana M. E. Harvell
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  4. Carol A. Sartorius
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  5. Kathryn B. Horwitz
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Correspondence to Joshua Chuck Harrell.

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Harrell, J.C., Dye, W.W., Harvell, D.M.E. et al. Contaminating cells alter gene signatures in whole organ versus laser capture microdissected tumors: a comparison of experimental breast cancers and their lymph node metastases. Clin Exp Metastasis 25, 81–88 (2008). https://doi.org/10.1007/s10585-007-9105-7

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  • DOI: https://doi.org/10.1007/s10585-007-9105-7

Keywords

  • Breast cancer
  • Estrogen receptors
  • Lymph node
  • Lymphatic vessel
  • Microarray
  • Metastasis
  • Progesterone receptors
  • Tumor xenografts
  • ZsGreen