MMP-14 (MT1-MMP) Is a Biomarker of Surgical Outcome and a Potential Mediator of Hearing Loss in Patients With Vestibular Schwannomas

被引:17
|
作者
Ren, Yin [1 ,2 ,3 ]
Hyakusoku, Hiroshi [1 ,2 ,4 ]
Sagers, Jessica E. [1 ,5 ,6 ]
Landegger, Lukas D. [1 ,2 ]
Welling, D. Bradley [1 ,2 ,5 ]
Stankovic, Konstantina M. [1 ,2 ,5 ,6 ]
机构
[1] Massachusetts Eye & Ear, Dept OtolaryngologyHead & Neck Surg, Eaton Peabody Labs, Boston, MA 02114 USA
[2] Harvard Med Sch, Dept OtolaryngologyHead & Neck Surg, Boston, MA 02115 USA
[3] Univ Calif San Diego, Div Otolaryngol Head & Neck Surg, San Diego, CA 92103 USA
[4] Yokosuka Kyosai Hosp, Dept Otorhinolaryngol, Yokosuka, Kanagawa, Japan
[5] Harvard Med Sch, Program Speech & Hearing Biosci & Technol, Boston, MA 02115 USA
[6] Harvard Univ, Harvard Program Therapeut Sci, Boston, MA 02115 USA
关键词
MMP-14; vestibular schwannoma; biomarker; hearing loss; surgical outcome; MATRIX METALLOPROTEINASE-2; GENE-EXPRESSION; INHIBITORS; MANAGEMENT; RESECTION; RECEPTOR; SURGERY; GROWTH; TUMORS; CELLS;
D O I
10.3389/fncel.2020.00191
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Improved biomarkers are needed for vestibular schwannoma (VS), the most common tumor of the cerebellopontine angle, as existing clinical biomarkers have poor predictive value. Factors such as tumor size or growth rate do not shed light on the pathophysiology of associated sensorineural hearing loss (SNHL) and suffer from low specificity and sensitivity, whereas histological markers only sample a fraction of the tumor and are difficult to ascertain before tumor treatment or surgical intervention. Proteases play diverse and critical roles in tumorigenesis and could be leveraged as a new class of VS biomarkers. Using a combination ofin silico,in vitro, andex vivoapproaches, we identified matrixmetalloprotease 14 (MMP-14; also known as MT1-MMP), from a panel of candidate proteases that were differentially expressed through the largest meta-analysis of human VS transcriptomes. The abundance and proteolytic activity of MMP-14 in the plasma and tumor secretions from VS patients correlated with clinical parameters and the degree of SNHL. Further, MMP-14 plasma levels correlated with surgical outcomes such as the extent of resection. Finally, the application of MMP-14 at physiologic concentrations to cochlear explant cultures led to damage to spiral ganglion neuronal fibers and synapses, thereby providing mechanistic insight into VS-associated SNHL. Taken together, MMP-14 represents a novel molecular biomarker that merits further validation in both diagnostic and prognostic applications for VS.
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页数:14
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共 48 条
  • [1] Ischemia-induced cleavage of cadherins in NRK cells requires MT1-MMP (MMP-14)
    Covington, MD
    Burghardt, RC
    Parrish, AR
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2006, 290 (01) : F43 - F51
  • [2] Increased serum level of membrane type 1-matrix metalloproteinase (MT1-MMP/MMP-14) in patients with breast cancer
    Laudanski, P.
    Swiatecka, J.
    Kozlowski, L.
    Lesniewska, M.
    Wojtukiewicz, M.
    Wolczynski, S.
    [J]. FOLIA HISTOCHEMICA ET CYTOBIOLOGICA, 2010, 48 (01) : 101 - 103
  • [3] Differential expression of MT1-MMP (MMP-14) and collagenase III (MMP-13) genes in normal and wounded rat corneas
    Ye, HQQ
    Maeda, M
    Yu, FSX
    Azar, DT
    [J]. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2000, 41 (10) : 2894 - 2899
  • [4] Differential patterns of stromelysin-2 (MMP-10) and MT1-MMP (MMP-14) expression in epithelial skin cancers
    Kerkelä, E
    Ala-aho, R
    Jeskanen, L
    Lohi, J
    Grénman, R
    Kähäri, VM
    Saarialho-Kere, U
    [J]. BRITISH JOURNAL OF CANCER, 2001, 84 (05) : 659 - 669
  • [5] Differential patterns of stromelysin-2 (MMP-10) and MT1-MMP (MMP-14) expression in epithelial skin cancers
    E Kerkelä
    R Ala-aho
    L Jeskanen
    J Lohi
    R Grénman
    V M-Kähäri
    U Saarialho-Kere
    [J]. British Journal of Cancer, 2001, 84 : 659 - 669
  • [6] Cellular mechanisms for human procollagenase-3 (MMP-13) activation - Evidence that MT1-MMP (MMP-14) and gelatinase A (MMP-2) are able to generate active enzyme
    Knauper, V
    Will, H
    LopezOtin, C
    Smith, B
    Atkinson, SJ
    Stanton, H
    Hembry, RM
    Murphy, G
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (29) : 17124 - 17131
  • [7] A monoclonal antibody interferes with TIMP-2 binding and incapacitates the MMP-2-activating function of multifunctional, pro-tumorigenic MMP-14/MT1-MMP
    Shiryaev, S. A.
    Remacle, A. G.
    Golubkov, V. S.
    Ingvarsen, S.
    Porse, A.
    Behrendt, N.
    Cieplak, P.
    Strongin, A. Y.
    [J]. ONCOGENESIS, 2013, 2 : e80 - e80
  • [8] MT1-MMP as a PET Imaging Biomarker for Pancreas Cancer Management
    Angel Morcillo, Miguel
    Garcia de Lucas, Angel
    Oteo, Marta
    Romero, Eduardo
    Magro, Natalia
    Ibanez, Marta
    Martinez, Alfonso
    Garaulet, Guillermo
    Arroyo, Alicia G.
    Pablo Lopez-Casas, Pedro
    Hidalgo, Manuel
    Mulero, Francisca
    Martinez-Torrecuadradae, Jorge
    [J]. CONTRAST MEDIA & MOLECULAR IMAGING, 2018,
  • [9] Synthesis and in vitro evaluation of 68Ga-labeled peptides for metalloproteinase (MT1-MMP/MMP-14) targeting on HT1080 cells
    Liolios, C.
    Bauder-Wuest, U.
    Schaefer, M.
    Kopka, K.
    [J]. EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2017, 44 : S522 - S522
  • [10] MT1-MMP - A potential drug target for the management of the obesity
    Asthana, Pallavi
    Guo, Xuanming
    Wong, Hoi Leong Xavier
    [J]. EXPERT OPINION ON THERAPEUTIC TARGETS, 2022,