Cancer of unknown primary stem-like cells model multi-organ metastasis and unveil liability to MEK inhibition.
Federica VerginelliAlberto PisacaneGennaro GambardellaAntonio D'AmbrosioErmes CandielloMarco FerrioMara PaneroLaura CasorzoSilvia BenvenutiEliano CascardiRebecca SenettaElena GeunaAndrea BalabioFilippo MontemurroAnna SapinoPaolo M ComoglioCarla BoccaccioPublished in: Nature communications (2021)
Cancers of unknown primary (CUPs), featuring metastatic dissemination in the absence of a primary tumor, are a biological enigma and a fatal disease. We propose that CUPs are a distinct, yet unrecognized, pathological entity originating from stem-like cells endowed with peculiar and shared properties. These cells can be isolated in vitro (agnospheres) and propagated in vivo by serial transplantation, displaying high tumorigenicity. After subcutaneous engraftment, agnospheres recapitulate the CUP phenotype, by spontaneously and quickly disseminating, and forming widespread established metastases. Regardless of different genetic backgrounds, agnospheres invariably display cell-autonomous proliferation and self-renewal, mostly relying on unrestrained activation of the MAP kinase/MYC axis, which confers sensitivity to MEK inhibitors in vitro and in vivo. Such sensitivity is associated with a transcriptomic signature predicting that more than 70% of CUP patients could be eligible to MEK inhibition. These data shed light on CUP biology and unveil an opportunity for therapeutic intervention.
Keyphrases
- pi k akt
- single cell
- randomized controlled trial
- induced apoptosis
- ejection fraction
- small cell lung cancer
- cell therapy
- signaling pathway
- squamous cell carcinoma
- cell cycle arrest
- total hip arthroplasty
- papillary thyroid
- stem cells
- prognostic factors
- mesenchymal stem cells
- oxidative stress
- machine learning
- squamous cell
- young adults
- lymph node metastasis
- patient reported