Clonal cooperation through soluble metabolite exchange facilitates metastatic outgrowth by modulating Allee effect.


Journal

Science advances
ISSN: 2375-2548
Titre abrégé: Sci Adv
Pays: United States
ID NLM: 101653440

Informations de publication

Date de publication:
15 09 2023
Historique:
medline: 18 9 2023
pubmed: 15 9 2023
entrez: 15 9 2023
Statut: ppublish

Résumé

Cancers feature substantial intratumoral heterogeneity of genetic and phenotypically distinct lineages. Although interactions between coexisting lineages are emerging as a potential contributor to tumor evolution, the extent and nature of these interactions remain largely unknown. We postulated that tumors develop ecological interactions that sustain diversity and facilitate metastasis. Using a combination of fluorescent barcoding, mathematical modeling, metabolic analysis, and in vivo models, we show that the Allee effect, i.e., growth dependency on population size, is a feature of tumor lineages and that cooperative ecological interactions between lineages alleviate the Allee barriers to growth in a model of triple-negative breast cancer. Soluble metabolite exchange formed the basis for these cooperative interactions and catalyzed the establishment of a polyclonal community that displayed enhanced metastatic dissemination and outgrowth in xenograft models. Our results highlight interclonal metabolite exchange as a key modulator of tumor ecology and a contributing factor to overcoming Allee effect-associated growth barriers to metastasis.

Identifiants

pubmed: 37713487
doi: 10.1126/sciadv.adh4184
doi:

Substances chimiques

Coloring Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

eadh4184

Auteurs

Benjamin J Hershey (BJ)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Sara Barozzi (S)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Fabrizio Orsenigo (F)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Simone Pompei (S)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Fabio Iannelli (F)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Stephan Kamrad (S)

Medical Research Council Toxicology Unit, Cambridge, UK.

Vittoria Matafora (V)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Federica Pisati (F)

Histopathology Unit, Cogentech S.C.A.R.L., Milan, Italy.

Ludovico Calabrese (L)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Giuseppe Fragale (G)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Giulia Salvadori (G)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Emanuele Martini (E)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Maria Grazia Totaro (MG)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Serena Magni (S)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Rui Guan (R)

Medical Research Council Toxicology Unit, Cambridge, UK.

Dario Parazzoli (D)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Paolo Maiuri (P)

University of Naples Federico II, Naples, Italy.

Angela Bachi (A)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

Kiran R Patil (KR)

Medical Research Council Toxicology Unit, Cambridge, UK.

Marco Cosentino Lagomarsino (M)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.
University of Milano, Milan, Italy.

Kristina M Havas (KM)

IFOM ETS The AIRC Institute of Molecular Oncology, Milan, Italy.

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Classifications MeSH