Mouse Tumor-Bearing Models as Preclinical Study Platforms for Oral Squamous Cell Carcinoma

被引:55
作者
Li, Qiang [1 ]
Dong, Heng [1 ,2 ]
Yang, Guangwen [1 ]
Song, Yuxian [1 ]
Mou, Yongbin [1 ,2 ]
Ni, Yanhong [1 ]
机构
[1] Nanjing Univ, Nanjing Stomatol Hosp, Med Sch, Cent Lab, Nanjing, Peoples R China
[2] Nanjing Univ, Nanjing Stomatol Hosp, Med Sch, Dept Oral Implantol, Nanjing, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2020年 / 10卷
关键词
mouse models; OSCC; chemical carcinogen-induced; transplanted; xenograft; syngeneic; HPV; genetically engineered models; LYMPH-NODE METASTASIS; HPV-RELATED HEAD; 4-NITROQUINOLINE; 1-OXIDE; ANIMAL-MODELS; IN-VITRO; 4-HYDROXYAMINOQUINOLINE; INITIATING ACTIVITY; THERAPEUTIC TARGET; XENOGRAFT MODEL; GENE-EXPRESSION;
D O I
10.3389/fonc.2020.00212
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Preclinical animal models of oral squamous cell carcinoma (OSCC) have been extensively studied in recent years. Investigating the pathogenesis and potential therapeutic strategies of OSCC is required to further progress in this field, and a suitable research animal model that reflects the intricacies of cancer biology is crucial. Of the animal models established for the study of cancers, mouse tumor-bearing models are among the most popular and widely deployed for their high fertility, low cost, and molecular and physiological similarity to humans, as well as the ease of rearing experimental mice. Currently, the different methods of establishing OSCC mouse models can be divided into three categories: chemical carcinogen-induced, transplanted and genetically engineered mouse models. Each of these methods has unique advantages and limitations, and the appropriate application of these techniques in OSCC research deserves our attention. Therefore, this review comprehensively investigates and summarizes the tumorigenesis mechanisms, characteristics, establishment methods, and current applications of OSCC mouse models in published papers. The objective of this review is to provide foundations and considerations for choosing suitable model establishment methods to study the relevant pathogenesis, early diagnosis, and clinical treatment of OSCC.
引用
收藏
页数:21
相关论文
共 204 条
  • [1] Gene expression analyses associated with malignant phenotypes of metastatic sub-clones derived from a mouse oral squamous cell carcinoma Sq-1979 cell line
    Adachi, Mitsutaka
    Mizuno-Kamiya, Masako
    Takayama, Eiji
    Kawaki, Harumi
    Inagaki, Toshihiro
    Sumi, Shigeki
    Motohashi, Masayuki
    Muramatsu, Yasunori
    Sumitomo, Shin-Ichiro
    Shikimori, Michio
    Yamazaki, Yutaka
    Kondoh, Nobuo
    [J]. ONCOLOGY LETTERS, 2018, 15 (03) : 3350 - 3356
  • [2] Human acute leukemia cells injected in NOD/LtSz-scid/IL-2Rγ null mice generate a faster and more efficient disease compared to other NOD/scid-related strains
    Agliano, Alice
    Martin-Padura, Ines
    Mancuso, Patrizia
    Marighetti, Paola
    Rabascio, Cristina
    Pruneri, Giancarlo
    Shultz, Leonard D.
    Bertolini, Francesco
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2008, 123 (09) : 2222 - 2227
  • [3] Downregulation of Keratin 76 Expression during Oral Carcinogenesis of Human, Hamster and Mouse
    Ambatipudi, Srikant
    Bhosale, Priyanka G.
    Heath, Emma
    Pandey, Manishkumar
    Kumar, Gaurav
    Kane, Shubhada
    Patil, Asawari
    Maru, Girish B.
    Desai, Rajiv S.
    Watt, Fiona M.
    Mahimkar, Manoj B.
    [J]. PLOS ONE, 2013, 8 (07):
  • [4] [Anonymous], 2018, ANTI-CANCER DRUG, DOI [DOI 10.3322/caac.20115, DOI 10.1097/CAD.0000000000000617]
  • [5] 4-Nitroquinoline 1-oxide forms 8-hydroxydeoxyguanosine in human fibroblasts through reactive oxygen species
    Arima, Yaeno
    Nishigori, Chikako
    Takeuchi, Toru
    Oka, Shigenori
    Morimoto, Kanehisa
    Utani, Atsushi
    Miyachi, Yoshiki
    [J]. TOXICOLOGICAL SCIENCES, 2006, 91 (02) : 382 - 392
  • [6] Orthotopic non-metastatic and metastatic oral cancer mouse models
    Bais, Manish V.
    Kukuruzinska, Maria
    Trackman, Philip C.
    [J]. ORAL ONCOLOGY, 2015, 51 (05) : 476 - 482
  • [7] Evaluation of hypoxia in a feline model of head and neck cancer using 64Cu-ATSM positron emission tomography/computed tomography
    Ballegeer, Elizabeth A.
    Madrill, Nicole J.
    Berger, Kevin L.
    Agnew, Dalen W.
    McNiel, Elizabeth A.
    [J]. BMC CANCER, 2013, 13
  • [8] Development of an oral cancer recurrence mouse model after surgical resection
    Behren, Andreas
    Kamenisch, York
    Muehlen, Sabrina
    Flechtenmacher, Christa
    Haberkorn, Uwe
    Hilber, Hermann
    Myers, Jeffrey N.
    Bergmann, Zazie
    Plinkert, Peter Karl
    Simon, Christian
    [J]. INTERNATIONAL JOURNAL OF ONCOLOGY, 2010, 36 (04) : 849 - 855
  • [9] CONVERSION OF 4-NITROQUINOLINE 1-OXIDE (4NQO) TO 4-HYDROXYAMINOQUINOLINE 1-OXIDE BY A DICUMAROL-RESISTANT HEPATIC-4NQO NITROREDUCATASE IN RATS AND MICE
    BENSON, AM
    [J]. BIOCHEMICAL PHARMACOLOGY, 1993, 46 (07) : 1217 - 1221
  • [10] Loss of TGF-β signaling and PTEN promotes head and neck squamous cell carcinoma through cellular senescence evasion and cancer-related inflammation
    Bian, Y.
    Hall, B.
    Sun, Z-J
    Molinolo, A.
    Chen, W.
    Gutkind, J. S.
    Waes, C. V.
    Kulkarni, A. B.
    [J]. ONCOGENE, 2012, 31 (28) : 3322 - 3332