Bibliometric analysis of personalized humanized mouse and Drosophila models for effective combinational therapy in cancer patients

Biochim Biophys Acta Mol Basis Dis. 2020 Oct 1;1866(10):165880. doi: 10.1016/j.bbadis.2020.165880. Epub 2020 Jun 24.

Abstract

Research performed using model organisms such as mice and the fruit fly, Drosophila melanogaster has significantly enhanced our knowledge about cancer biology and the fundamental processes of cancer. This is because the major biological properties and genes associated with cancer including signaling pathways, oncogenes, tumor suppressors, and other regulators of cell growth and proliferation are evolutionary conserved. This review provides bibliometric analysis of research productivity, and performance of authors, institutions, countries, and journals associated with personalized animal cancer models, focussing on the role of Drosophila in cancer research, thus highlighting emerging trends in the field. A total of 1469 and 2672 original articles and reviews for Drosophila cancer model and patient-derived xenograft (PDX) respectively, were retrieved from the Scopus database and the most cited papers were thoroughly analyzed. Our analysis indicates a steadily increasing productivity of the animal models and especially of mouse models in cancer research. In addition to the many different systems that address almost all aspects of tumor research in humanized animal models, a trend towards using tailored screening platforms with Drosophila models in particular will become widespread in the future. Having Drosophila models that recapitulate major genetic aspects of a given tumor will enable the development and validation of novel therapeutic strategies for specific cancers, and provide a platform for screening small molecule inhibitors and other anti-tumor compounds. The combination of Drosophila cancer models and mouse PDX models particularly is highly promising and should be one of the major research strategies the future.

Keywords: Cancer; Drosophila; Model organism; Oncogene; Ras; Tumor suppressor.

Publication types

  • Review

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Bibliometrics*
  • Combined Modality Therapy / methods
  • Disease Models, Animal*
  • Drosophila
  • Humans
  • Mice
  • Neoplasms / genetics
  • Neoplasms / pathology
  • Neoplasms / therapy*
  • Oncogenes / genetics*
  • Xenograft Model Antitumor Assays*