Author
Listed:
- Federica Verginelli
(Laboratory of Cancer Stem Cell Research, Candiolo Cancer Institute, FPO-IRCCS)
- Alberto Pisacane
(Unit of Pathology, Candiolo Cancer Institute, FPO-IRCCS)
- Gennaro Gambardella
(Telethon Institute of Genetics and Medicine (TIGEM)
University of Naples Federico II, Department of Chemical Materials and Industrial Engineering)
- Antonio D’Ambrosio
(Laboratory of Cancer Stem Cell Research, Candiolo Cancer Institute, FPO-IRCCS)
- Ermes Candiello
(Laboratory of Cancer Stem Cell Research, Candiolo Cancer Institute, FPO-IRCCS)
- Marco Ferrio
(Laboratory of Cancer Stem Cell Research, Candiolo Cancer Institute, FPO-IRCCS)
- Mara Panero
(Unit of Pathology, Candiolo Cancer Institute, FPO-IRCCS)
- Laura Casorzo
(Unit of Pathology, Candiolo Cancer Institute, FPO-IRCCS)
- Silvia Benvenuti
(Laboratory of Exploratory Research and Molecular Cancer Therapy, Candiolo Cancer Institute, FPO-IRCCS)
- Eliano Cascardi
(Unit of Pathology, Candiolo Cancer Institute, FPO-IRCCS
University of Turin Medical School)
- Rebecca Senetta
(Unit of Pathology, Candiolo Cancer Institute, FPO-IRCCS)
- Elena Geuna
(Multidisciplinary Oncology Outpatient Clinic, Candiolo Cancer Institute, FPO-IRCCS)
- Andrea Ballabio
(Telethon Institute of Genetics and Medicine (TIGEM)
University of Naples Federico II, Department of Medical and Translation Science
Jan and Dan Duncan Neurological Research Institute, Texas Children Hospital)
- Filippo Montemurro
(Multidisciplinary Oncology Outpatient Clinic, Candiolo Cancer Institute, FPO-IRCCS)
- Anna Sapino
(Unit of Pathology, Candiolo Cancer Institute, FPO-IRCCS
University of Turin Medical School)
- Paolo M. Comoglio
(Laboratory of Exploratory Research and Molecular Cancer Therapy, Candiolo Cancer Institute, FPO-IRCCS
IFOM, FIRC Institute of Molecular Oncology)
- Carla Boccaccio
(Laboratory of Cancer Stem Cell Research, Candiolo Cancer Institute, FPO-IRCCS
University of Turin Medical School)
Abstract
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.
Suggested Citation
Federica Verginelli & Alberto Pisacane & Gennaro Gambardella & Antonio D’Ambrosio & Ermes Candiello & Marco Ferrio & Mara Panero & Laura Casorzo & Silvia Benvenuti & Eliano Cascardi & Rebecca Senetta , 2021.
"Cancer of unknown primary stem-like cells model multi-organ metastasis and unveil liability to MEK inhibition,"
Nature Communications, Nature, vol. 12(1), pages 1-16, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-22643-w
DOI: 10.1038/s41467-021-22643-w
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