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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Head and neck cancer patient-derived xenograft models - A systematic review

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Autor(es):
Schuch, Lauren F. [1] ; Silveira, Felipe M. [1] ; Wagner, Vivian P. [1] ; Borgato, Gabriell B. [1] ; Rocha, Guilherme Z. [1] ; Castilho, Rogerio M. [2, 3] ; Vargas, Pablo A. [1] ; Martins, Manoela D. [1, 4]
Número total de Autores: 8
Afiliação do(s) autor(es):
[1] Univ Estadual Campinas, Piracicaba Dent Sch, Dept Oral Diag, Piracicaba, SP - Brazil
[2] Univ Michigan, Sch Dent, Lab Epithelial Biol, Dept Periodont & Oral Med, Ann Arbor, MI 48109 - USA
[3] Univ Michigan, Comprehens Canc Ctr, Ann Arbor, MI 48109 - USA
[4] Univ Fed Rio Grande do Sul, Sch Dent, Dept Oral Pathol, Porto Alegre, RS - Brazil
Número total de Afiliações: 4
Tipo de documento: Artigo de Revisão
Fonte: CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY; v. 155, NOV 2020.
Citações Web of Science: 0
Resumo

Background: Patient-derived xenograft (PDX) involve the direct surgical transfer of fresh human tumor samples to immunodeficient mice. This systematic review aimed to identify publications of head and neck cancer PDX (HNC-PDX) models, describing the main methodological characteristics and outcomes. Methods: An electronic search was undertaken in four databases, including publications having used HNC-PDX. Data were analyzed descriptively. Results: 63 articles were yielded. The nude mouse was one most commonly animal model used (38.8 %), and squamous cell carcinoma accounted for the majority of HNC-PDX (80.6 %). Tumors were mostly implanted in the flank (86.3 %), and the latency period ranged from 30 to 401 days. The successful rate ranged from 17 % to 100 %. Different drugs and pathways were identified. Conclusion: HNC-PDX appears to significantly recapitulate the morphology of the original HNC and represents a valuable method in translational research for the assessment of the in vivo effect of novel therapies for HNC. (AU)

Processo FAPESP: 16/21785-4 - Relação da via de sinalização BDNF/TRKB com a agressividade e perfil de células tronco tumorais de neoplasias malignas de glândula salivar
Beneficiário:Vivian Petersen Wagner
Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado