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Stresses in the metastatic cascade: molecular mechanisms and therapeutic opportunities

Author(s): Shen, Minhong; Kang, Yibin

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dc.contributor.authorShen, Minhong-
dc.contributor.authorKang, Yibin-
dc.date.accessioned2022-01-25T14:52:40Z-
dc.date.available2022-01-25T14:52:40Z-
dc.date.issued2020-12en_US
dc.identifier.citationShen, Minhong, Kang, Yibin. (2020). Stresses in the metastatic cascade: molecular mechanisms and therapeutic opportunities. Genes & development, 34 (23-24), 1577 - 1598. doi:10.1101/gad.343251.120en_US
dc.identifier.issn0890-9369-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/pr1ns0kx2p-
dc.description.abstractMetastasis is the ultimate "survival of the fittest" test for cancer cells, as only a small fraction of disseminated tumor cells can overcome the numerous hurdles they encounter during the transition from the site of origin to a distinctly different distant organ in the face of immune and therapeutic attacks and various other stresses. During cancer progression, tumor cells develop a variety of mechanisms to cope with the stresses they encounter, and acquire the ability to form metastases. Restraining these stress-releasing pathways could serve as potentially effective strategies to prevent or reduce metastasis and improve the survival of cancer patients. Here, we provide an overview of the tumor-intrinsic, microenvironment- and treatment-induced stresses that tumor cells encounter in the metastatic cascade and the molecular pathways they develop to relieve these stresses. We also summarize the preclinical and clinical studies that evaluate the potential therapeutic benefit of targeting these stress-relieving pathways.en_US
dc.format.extent1577 - 1598en_US
dc.languageengen_US
dc.language.isoen_USen_US
dc.relation.ispartofGenes & Developmenten_US
dc.rightsFinal published version. This is an open access article.en_US
dc.titleStresses in the metastatic cascade: molecular mechanisms and therapeutic opportunitiesen_US
dc.typeJournal Articleen_US
dc.identifier.doidoi:10.1101/gad.343251.120-
dc.identifier.eissn1549-5477-
pu.type.symplectichttp://www.symplectic.co.uk/publications/atom-terms/1.0/journal-articleen_US

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