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Investigation of female survival benefit in metastatic melanoma
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  • Regular Article
  • Open access
  • Published: 30 July 1999

Investigation of female survival benefit in metastatic melanoma

  • B Richardson1,
  • A Price2,
  • M Wagner1,
  • V Williams1,
  • P Lorigan4,
  • S Browne4,
  • J G Miller3 &
  • …
  • S Mac Neil1 

British Journal of Cancer volume 80, pages 2025–2033 (1999)Cite this article

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Summary

Epidemiological studies show female survival benefit in advanced metastatic melanoma. In investigating a possible mechanism for this female survival benefit, we have previously reported that the female steroid 17β-oestradiol significantly reduces invasion of a human melanoma cell line (A375-SM cells) and ocular melanoma cells through fibronectin. Neither cell type was found to possess oestrogen receptor-α. The aim of the current study was to obtain further information on the extent to which progression of cutaneous melanoma might be sex steroid sensitive by (a) examining the relationship between circulating sex steroids, sex hormone binding globulin and disease progression; (b) examining the relationship between sex steroid structure and the ability of steroids to reduce invasion of a melanoma cell line in vitro; and (c) examining the effects of sex steroids on proliferation of these cells in vitro. We report a significant reduction in circulating oestrone with disease progression in male but not female patients. Examining steroids for their ability to inhibit invasion of A375-SM cells through fibronectin in vitro, oestrogenic compounds (17β-oestradiol and oestrone) were found to inhibit invasion; in this respect, oestrone was approximately 50 times more potent than 17β-oestradiol; steroids lacking the benzene ring structure did not inhibit invasion, indeed dehydroepiandrosterone (DHEA) which acts as a precursor to androgenic steroids significantly enhanced invasion. Proliferation of A375-SM cells was unaffected by 17β-oestradiol, oestrone or dihydrotestosterone when cells were cultured on plastic; in contrast, all three steroids induced modest proliferation of cells when grown on fibronectin with dihydrotestosterone the most mitogenic of the three steroids. These data are consistent with sex steroids playing a role in melanoma progression.

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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. University Department of Medicine, Northern General Hospital Trust, Sheffield, S5 7AU, UK

    B Richardson, M Wagner, V Williams & S Mac Neil

  2. Department of Clinical Chemistry, Northern General Hospital Trust, Sheffield, S5 7AU, UK

    A Price

  3. Department of Plastic and Reconstructive Surgery, Northern General Hospital Trust, Sheffield, S5 7AU, UK

    J G Miller

  4. Department of Clinical Oncology, Weston Park Hospital, Sheffield, S10, UK

    P Lorigan & S Browne

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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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Cite this article

Richardson, B., Price, A., Wagner, M. et al. Investigation of female survival benefit in metastatic melanoma. Br J Cancer 80, 2025–2033 (1999). https://doi.org/10.1038/sj.bjc.6690637

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  • Received: 08 September 1998

  • Revised: 19 February 1999

  • Accepted: 23 February 1999

  • Published: 30 July 1999

  • Issue date: 01 August 1999

  • DOI: https://doi.org/10.1038/sj.bjc.6690637

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Keywords

  • melanoma
  • invasion
  • oestrogen
  • testosterone
  • oestrogen receptor-β

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