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Matrix metalloproteinases (MMPs) in fresh human prostate tumour tissue and organ-cultured prostate tissue: Levels of collagenolytic and gelatinolytic MMPs are low, variable and different in fresh tissue versus organ-cultured tissue
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  • Published: 17 April 2001

Matrix metalloproteinases (MMPs) in fresh human prostate tumour tissue and organ-cultured prostate tissue: Levels of collagenolytic and gelatinolytic MMPs are low, variable and different in fresh tissue versus organ-cultured tissue

  • J Varani1,
  • Y Hattori1,
  • M K Dame1,
  • T Schmidt1,
  • H S Murphy2,
  • K J Johnson1 &
  • …
  • K J Wojno3 

British Journal of Cancer volume 84, pages 1076–1083 (2001)Cite this article

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Abstract

Prostate tissue was obtained from 22 radical prostatectomies (performed for clinical management of prostate carcinoma) immediately after surgery. A small piece of tissue was fixed immediately in formalin and used for routine histology while a second piece was frozen in OCT and used for immuno-histochemistry. Another small piece was used for isolation of epithelial and stromal cells. The remainder of the tissue was cut into 2 × 2 mm pieces and incubated in organ culture for 8 days. In organ culture, non-malignant, basal epithelial cells underwent a proliferative response. This was accompanied by de-differentiation of glandular structures and by migration of epithelial cells across the surface of the tissue. Erosion of the basement membrane could also be seen in places, but was not widespread. Invasion of epithelial cells into the adjacent stroma was not evident. Production of matrix metalloproteinases (MMPs) with gelatinolytic activity or collagenolytic activity was assessed in organ culture and compared to expression patterns in fresh tissue. MMP-1 (interstitial collagenase) and MMP-9 (92-kDa gelatinase B) were undetectable or low in fresh tissue specimens. Both enzymes were detected in organ culture and both increased over time. Even after 6 days, however, there was only a low level of gelatin-hydrolytic activity and no measurable collagen-hydrolytic activity. In past studies we used organ cultures of normal skin and malignant skin tumours (basal cell carcinomas) to help elucidate the role of collagenolytic and gelatinolytic MMPs in epithelial cell invasion (Varani et al, 2000). Compared to MMP levels observed in skin, levels of these enzymes in prostate are low. The low level of collagenolytic and gelatinolytic MMPs in fresh prostate tissue and in organ-cultured prostate tissue may help explain why there is little tissue destruction in many primary prostate tumours and why the majority of such tumours remain confined to the prostate for extended periods. © 2001 Cancer Research Campaign

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  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

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Authors and Affiliations

  1. The Department of Pathology, The University of Michigan Medical School, Ann Arbor, 48109, Michigan

    J Varani, Y Hattori, M K Dame, T Schmidt & K J Johnson

  2. Department of Pathology and Laboratory Medicine, VAMC – Ann Arbor, Ann Arbor, 48105, Michigan

    H S Murphy

  3. The Department of Pathology, St. John Hospital and Medical Center, Detroit, 48236-2172, Michigan

    K J Wojno

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From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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Varani, J., Hattori, Y., Dame, M. et al. Matrix metalloproteinases (MMPs) in fresh human prostate tumour tissue and organ-cultured prostate tissue: Levels of collagenolytic and gelatinolytic MMPs are low, variable and different in fresh tissue versus organ-cultured tissue. Br J Cancer 84, 1076–1083 (2001). https://doi.org/10.1054/bjoc.2000.1712

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  • Received: 21 August 2000

  • Revised: 14 December 2000

  • Accepted: 19 December 2000

  • Published: 17 April 2001

  • Issue date: 20 April 2001

  • DOI: https://doi.org/10.1054/bjoc.2000.1712

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Keywords

  • prostate
  • carcinoma
  • organ culture
  • matrix metalloproteinases
  • collagenase
  • gelatinase

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