| Literature DB >> 31287989 |
Nikolas G Balanis1, Katherine M Sheu1, Favour N Esedebe1, Saahil J Patel1, Bryan A Smith2, Jung Wook Park2, Salwan Alhani1, Brigitte N Gomperts3, Jiaoti Huang4, Owen N Witte5, Thomas G Graeber6.
Abstract
Small-cell neuroendocrine cancers (SCNCs) are an aggressive cancer subtype. Transdifferentiation toward an SCN phenotype has been reported as a resistance route in response to targeted therapies. Here, we identified a convergence to an SCN state that is widespread across epithelial cancers and is associated with poor prognosis. More broadly, non-SCN metastases have higher expression of SCN-associated transcription factors than non-SCN primary tumors. Drug sensitivity and gene dependency screens demonstrate that these convergent SCNCs have shared vulnerabilities. These common vulnerabilities are found across unannotated SCN-like epithelial cases, small-round-blue cell tumors, and unexpectedly in hematological malignancies. The SCN convergent phenotype and common sensitivity profiles with hematological cancers can guide treatment options beyond tissue-specific targeted therapies.Entities:
Keywords: Dependency Map (depmap); RNA interference screen; SCLC; TCGA; blood cancer; drug sensitivity screen; pan-cancer signatures; pharmacogenomics; small-cell neuroendocrine; transdifferentiation
Mesh:
Year: 2019 PMID: 31287989 PMCID: PMC6703903 DOI: 10.1016/j.ccell.2019.06.005
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743