Immunohistochemical Expression of Platelet-Derived Growth Factor Receptor β (PDGFR-β) in Canine Cutaneous Peripheral Nerve Sheath Tumors: A Preliminary Study

被引:0
|
作者
Aluai-Cunha, Catarina [1 ]
Matos, Augusto [1 ,2 ]
Amorim, Irina [3 ,4 ,5 ]
Carvalho, Fatima [3 ]
Rema, Alexandra [3 ]
Santos, Andreia [1 ,2 ]
机构
[1] Univ Porto, Inst Biomed Sci Abel Salazar ICBAS, Dept Vet Clin, R Jorge Viterbo Ferreira 228, P-4050313 Porto, Portugal
[2] Food & Agr Sci & Technol Inst ICETA, Anim Sci & Study Ctr CECA, Apartado 55142, P-4051401 Porto, Portugal
[3] Univ Porto, Inst Biomed Sci Abel Salazar ICBAS, Dept Pathol & Mol Immunol, R Jorge Viterbo Ferreira 228, P-4050313 Porto, Portugal
[4] Univ Porto, Inst Mol Pathol & Immunol IPATIMUP, R Julio Amaral de Carvalho 45, P-4200135 Porto, Portugal
[5] Univ Porto, Inst Res & Innovat Hlth I3S, R Alfredo Allen 208, P-4200135 Porto, Portugal
关键词
dog; Ki-67; PDGFR-beta; PNST; sarcomas; SOFT-TISSUE SARCOMAS; CANCER; ACTIVATION; INVASION; PATHWAY; TARGETS; BIOLOGY; ALPHA; DOGS;
D O I
10.3390/vetsci9070345
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
As in humans, the prevalence of tumors in companion animals is increasing dramatically and there is a strong need for research on new pharmacological agents particularly for the treatment of those tumors that are resistant to conventional chemotherapy agents such as soft tissue sarcomas (STS). Because malignant (MPNST) and benign peripheral nerve sheath tumors (BPNST) are relatively common STS in dogs, the aim of this retrospective study was to evaluate the immunohistochemical (IHC) expression of PDGFR-beta, contributing to its characterization as a potential target for their treatment. A total of 19 samples were included, 9 histologically classified as benign and the other 10 as malignant. The results showed diffuse immunoexpression in the cytoplasm of neoplastic cells. Six (66.7%) BPNST expressed the receptor in less than 25% of neoplastic cells and only three (33.3%) exhibited labelling in more than 25% of neoplastic cells. In contrast, all MPNST expressed PDGFR-beta, and in 8 (80%) of these samples, the receptor was expressed in more than 25% of neoplastic cells, and only 2 (20%) cases expressed the receptor in less than 25% of neoplastic cells. PDGFR-beta expression was significantly higher in MPNST and larger tumors, suggesting that drugs able to inhibit the activity of this tyrosine kinase receptor, such as toceranib, may be considered in the approach of unresectable tumors and/or in the context of adjuvant or neoadjuvant therapies.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] Expression of vascular endothelial growth factor (VEGF) and platelet-derived growth factor receptor-β (PDGFR-β) in human gliomas
    J. V. Lafuente
    B. Adán
    K. Alkiza
    J. M. Garibi
    M. Rossi
    F. F. Cruz-Sánchez
    [J]. Journal of Molecular Neuroscience, 1999, 13 : 177 - 185
  • [2] Expression of vascular endothelial growth factor (VEGF) and platelet-derived growth factor receptor-β (PDGFR-β) in human gliomas
    Lafuente, JV
    Adán, B
    Alkiza, K
    Garibi, JM
    Rossi, M
    Cruz-Sánchez, FF
    [J]. JOURNAL OF MOLECULAR NEUROSCIENCE, 1999, 13 (1-2) : 177 - 185
  • [3] Both platelet-derived growth factor receptor (PDGFR)-α and PDGFR-β promote murine fibroblast cell migration
    Yu, JH
    Moon, A
    Kim, HRC
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 282 (03) : 697 - 700
  • [4] Platelet-derived growth factor receptor alpha (pdgfr-α) gene in zebrafish embryonic development
    Liu, LH
    Chong, SW
    Balasubramaniyan, NV
    Korzh, V
    Ge, RW
    [J]. MECHANISMS OF DEVELOPMENT, 2002, 116 (1-2) : 227 - 230
  • [5] Platelet-derived growth factor receptor β (PDGFRβ) expression in human peritoneum
    Seeger, Harald
    Braun, Niko
    Latus, Joerg
    Alscher, M. Dominik
    Fritz, Peter
    Edenhofer, Ilka
    Biegger, Dagmar
    Lindenmeyer, Maja
    Wuthrich, Rudolf P.
    Segerer, Stephan
    [J]. SWISS MEDICAL WEEKLY, 2014, 144 : 30S - 30S
  • [6] Molecular Cloning of the Human Platelet-Derived Growth Factor Receptor β (PDGFR-β) Promoter and Drug Targeting of the G-Quadruplex-Forming Region To Repress PDGFR-β Expression
    Qin, Yong
    Fortin, Jessica S.
    Tye, Denise
    Gleason-Guzman, Mary
    Brooks, Tracy A.
    Hurley, Laurence H.
    [J]. BIOCHEMISTRY, 2010, 49 (19) : 4208 - 4219
  • [7] Lack of expression of platelet-derived growth factor receptor beta (PDGFRβ) in Langerhans cell tumors:: An in situ hybridization study
    George, TI
    West, RB
    Blais, S
    Montgomery, KD
    Gotlib, J
    van de Rijn, M
    Arber, DA
    [J]. MODERN PATHOLOGY, 2006, 19 : 227A - 227A
  • [8] Lack of expression of platelet-derived growth factor receptor beta (PDGFRβ) in langerhans cell tumors:: An in situ hybridization study
    George, TI
    Mest, RB
    Blais, S
    Montgomery, K
    Gotlib, J
    van de Rijn, M
    Arber, DA
    [J]. LABORATORY INVESTIGATION, 2006, 86 : 227A - 227A
  • [9] Immunohistochemical analysis of platelet-derived growth factor receptor (PDGFR)-beta in dermatofibrosarcoma protuberans and dermatofibroma
    Hutchens, K.
    Alkan, S.
    [J]. JOURNAL OF CUTANEOUS PATHOLOGY, 2008, 35 (01) : 136 - 136
  • [10] Expression of Platelet-Derived Growth Factor Receptor α (PDGFRα) and Vascular Endothelial Growth Factor (VEGF) in Intravenous Leiomyomatosis (IVL): An Immunohistochemical Study of 29 Cases
    McDonald, A. G.
    Della Pelle, P.
    De Nictolis, M.
    Garcia-Fernandez, E.
    Hardisson, D.
    Prat, J.
    Oliva, E.
    [J]. LABORATORY INVESTIGATION, 2009, 89 : 228A - 228A