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Autor(en) / Beteiligte
Titel
Modeling prostate cancer: What does it take to build an ideal tumor model?
Ist Teil von
  • Cancer letters, 2022-09, Vol.543, p.215794-215794, Article 215794
Ort / Verlag
Clare: Elsevier B.V
Erscheinungsjahr
2022
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Prostate cancer is frequently characterized as a multifocal disease with great intratumoral heterogeneity as well as a high propensity to metastasize to bone. Consequently, modeling prostate tumor has remained a challenging task for researchers in this field. In the past decades, genomic advances have led to the identification of key molecular alterations in prostate cancer. Moreover, resistance towards second-generation androgen-deprivation therapy, namely abiraterone and enzalutamide has unveiled androgen receptor-independent diseases with distinctive histopathological and clinical features. In this review, we have critically evaluated the commonly used preclinical models of prostate cancer with respect to their capability of recapitulating the key genomic alterations, histopathological features and bone metastatic potential of human prostate tumors. In addition, we have also discussed the potential use of the emerging organoid models in prostate cancer research, which possess clear advantages over the commonly used preclinical tumor models. We anticipate that no single model can faithfully recapitulate the complexity of prostate cancer, and thus, propose the use of a cost- and time-efficient integrated tumor modeling approach for future prostate cancer investigations. •Critical evaluation of the commonly used and emerging preclinical models of prostate cancer.•The ability of these models to capture the diverse genomic alterations of prostate cancers.•The ability of these models in recapitulating histopathological and clinical features of prostate cancers.•The proposal of an integrative tumor modeling strategy as a time and cost-efficient approach for prostate cancer research.
Sprache
Englisch
Identifikatoren
ISSN: 0304-3835
eISSN: 1872-7980
DOI: 10.1016/j.canlet.2022.215794
Titel-ID: cdi_proquest_miscellaneous_2678746096

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