Non-murine models to investigate tumor-immune interactions in head and neck cancer

Carlos Rossa1,2, Nisha J D'Silva3,4

  • 1Department of Diagnosis and Surgery, UNESP-State University of Sao Paulo, School of Dentistry at Araraquara, Araraquara, SP, Brazil. c.rossa@unesp.br.

Oncogene
|March 16, 2019
PubMed

Insights

Non-murine models offer unique insights into head and neck cancer (HNC) tumor-immune interactions. This review explores how these models can improve the translation of pre-clinical findings to clinical efficacy for HNC therapies.

Area of Science:

  • Oncology
  • Immunology
  • Comparative Medicine

Background:

  • The immune system significantly influences solid tumor progression and treatment response.
  • Immune-based therapies, including those for head and neck cancer (HNC), show promise but face challenges in clinical translation.
  • Pre-clinical models are crucial for developing novel cancer therapies, yet often fail to predict clinical outcomes.

Purpose of the Study:

  • To review the immune-related aspects of non-murine pre-clinical models for head and neck cancer (HNC).
  • To highlight the potential of non-murine models in studying tumor-immune interactions relevant to HNC.
  • To address the limitations of current pre-clinical models in replicating clinical trial efficacy.

Main Methods:

  • Literature review focusing on non-murine models (dog, cat, pig, zebrafish, frog).
  • Analysis of immune-related characteristics of these models.
  • Evaluation of their suitability for studying HNC tumor-immune interactions.

Main Results:

  • Non-murine models possess distinct immunological features that can offer unique advantages over traditional murine models.
  • These models can provide valuable insights into HNC etiology, therapeutic strategies, and complex tumor-immune system dynamics.
  • Specific non-murine species present opportunities for investigating aspects of HNC not fully captured by current research.

Conclusions:

  • Non-murine models represent a valuable, underutilized resource for advancing HNC research.
  • Further investigation into these models could bridge the gap between pre-clinical efficacy and clinical outcomes.
  • Incorporating diverse non-murine models may enhance the development of more effective HNC immunotherapies.

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