Comparative gene expression profiling of ADAMs, MMPs, TIMPs, EMMPRIN, EGF-R and VEGFA in low grade meningioma

  • Authors:
    • Harcharan K. Rooprai
    • Andrew J. Martin
    • Andrew King
    • Usha D. Appadu
    • Huw Jones
    • Richard P. Selway
    • Richard W. Gullan
    • Geoffrey J. Pilkington
  • View Affiliations

  • Published online on: October 18, 2016     https://doi.org/10.3892/ijo.2016.3739
  • Pages: 2309-2318
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Abstract

MMPs (matrix metalloproteinases), ADAMs (a disintegrin and metalloproteinase) and TIMPs (tissue inhibitors of metalloproteinases) are implicated in invasion and angiogenesis: both are tissue remodeling processes involving regulated proteolysis of the extracellular matrix, growth factors and their receptors. The expression of these three groups and their correlations with clinical behaviour has been reported in gliomas but a similar comprehensive study in meningiomas is lacking. In this study, we aimed to evaluate the patterns of expression of 23 MMPs, 4 TIMPs, 8 ADAMs, selective growth factors and their receptors in 17 benign meningiomas using a quantitative real-time polymerase chain reaction (qPCR). Results indicated very high gene expression of 13 proteases, inhibitors and growth factors studied: MMP2 and MMP14, TIMP-1, -2 and -3, ADAM9, 10, 12, 15 and 17, EGF-R, EMMPRIN and VEGF-A, in almost every meningioma. Expression pattern analysis showed several positive correlations between MMPs, ADAMs, TIMPs and growth factors. Furthermore, our findings suggest that expression of MMP14, ADAM9, 10, 12, 15 and 17, TIMP-2, EGF-R and EMMPRIN reflects histological subtype of meningioma such that fibroblastic subtype had the highest mRNA expression, transitional subtype was intermediate and meningothelial type had the lowest expression. In conclusion, this is the first comprehensive study characterizing gene expression of 8 ADAMs in meningiomas. These neoplasms, although by histological definition benign, have invasive potential. Taken together, the selected elevated gene expression pattern may serve to identify targets for therapeutic intervention or indicators of biological progression and recurrence.
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December-2016
Volume 49 Issue 6

Print ISSN: 1019-6439
Online ISSN:1791-2423

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Spandidos Publications style
Rooprai HK, Martin AJ, King A, Appadu UD, Jones H, Selway RP, Gullan RW and Pilkington GJ: Comparative gene expression profiling of ADAMs, MMPs, TIMPs, EMMPRIN, EGF-R and VEGFA in low grade meningioma. Int J Oncol 49: 2309-2318, 2016
APA
Rooprai, H.K., Martin, A.J., King, A., Appadu, U.D., Jones, H., Selway, R.P. ... Pilkington, G.J. (2016). Comparative gene expression profiling of ADAMs, MMPs, TIMPs, EMMPRIN, EGF-R and VEGFA in low grade meningioma. International Journal of Oncology, 49, 2309-2318. https://doi.org/10.3892/ijo.2016.3739
MLA
Rooprai, H. K., Martin, A. J., King, A., Appadu, U. D., Jones, H., Selway, R. P., Gullan, R. W., Pilkington, G. J."Comparative gene expression profiling of ADAMs, MMPs, TIMPs, EMMPRIN, EGF-R and VEGFA in low grade meningioma". International Journal of Oncology 49.6 (2016): 2309-2318.
Chicago
Rooprai, H. K., Martin, A. J., King, A., Appadu, U. D., Jones, H., Selway, R. P., Gullan, R. W., Pilkington, G. J."Comparative gene expression profiling of ADAMs, MMPs, TIMPs, EMMPRIN, EGF-R and VEGFA in low grade meningioma". International Journal of Oncology 49, no. 6 (2016): 2309-2318. https://doi.org/10.3892/ijo.2016.3739