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Advanced in vitro models for renal cell carcinoma therapy design

  • Valentin Mieville
  • , Arjan W. Griffioen
  • , Daniel Benamran
  • , Patrycja Nowak-Sliwinska*
  • *Corresponding author for this work
  • University of Geneva
  • Translational Research Center in Oncohaematology, Geneva, Switzerland
  • Amsterdam UMC

Research output: Contribution to journalReview articleAcademicpeer-review

17 Downloads (Pure)

Abstract

Renal cell carcinoma (RCC) and its principal subtype, clear cell RCC, are the most diagnosed kidney cancer. Despite substantial improvement over the last decades, current pharmacological intervention still fails to achieve long-term therapeutic success. RCC is characterized by a high intra- and inter-tumoral heterogeneity and is heavily influenced by the crosstalk of the cells composing the tumor microenvironment, such as cancer-associated fibroblasts, endothelial cells and immune cells. Moreover, multiple physicochemical properties such as pH, interstitial pressure or oxygenation may also play an important role. These elements are often poorly recapitulated in in vitro models used for drug development. This inadequate recapitulation of the tumor is partially responsible for the current lack of an effective and curative treatment. Therefore, there are needs for more complex in vitro or ex vivo drug screening models. In this review, we discuss the current state-of-the-art of RCC models and suggest strategies for their further development.
Original languageEnglish
Article number188942
JournalBIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER
Volume1878
Issue number5
DOIs
Publication statusPublished - 1 Sept 2023

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Angiogenesis
  • Cancer-associated fibroblasts
  • Hypoxia
  • Immune system
  • Microfluidic device
  • Organ-on-chip
  • Organoids
  • Renal cell carcinoma
  • Screening platform
  • Tumor microenvironment
  • pH

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