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A Wnt-producing niche drives proliferative potential and progression in lung adenocarcinoma.
Tammela, Tuomas; Sanchez-Rivera, Francisco J; Cetinbas, Naniye Malli; Wu, Katherine; Joshi, Nikhil S; Helenius, Katja; Park, Yoona; Azimi, Roxana; Kerper, Natanya R; Wesselhoeft, R Alexander; Gu, Xin; Schmidt, Leah; Cornwall-Brady, Milton; Yilmaz, Ömer H; Xue, Wen; Katajisto, Pekka; Bhutkar, Arjun; Jacks, Tyler.
Afiliação
  • Tammela T; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Sanchez-Rivera FJ; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Cetinbas NM; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Wu K; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Joshi NS; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Helenius K; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Park Y; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Azimi R; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Kerper NR; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Wesselhoeft RA; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Gu X; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Schmidt L; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Cornwall-Brady M; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Yilmaz ÖH; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Xue W; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
  • Katajisto P; RNA Therapeutics Institute, Program in Molecular Medicine, and Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
  • Bhutkar A; Institute of Biotechnology, University of Helsinki, 00014 Helsinki, Finland.
  • Jacks T; Department of Biosciences and Nutrition, Karolinska Institutet, 14183 Stockholm, Sweden.
Nature ; 545(7654): 355-359, 2017 05 18.
Article em En | MEDLINE | ID: mdl-28489818
ABSTRACT
The heterogeneity of cellular states in cancer has been linked to drug resistance, cancer progression and the presence of cancer cells with properties of normal tissue stem cells. Secreted Wnt signals maintain stem cells in various epithelial tissues, including in lung development and regeneration. Here we show that mouse and human lung adenocarcinomas display hierarchical features with two distinct subpopulations, one with high Wnt signalling activity and another forming a niche that provides the Wnt ligand. The Wnt responder cells showed increased tumour propagation ability, suggesting that these cells have features of normal tissue stem cells. Genetic perturbation of Wnt production or signalling suppressed tumour progression. Small-molecule inhibitors targeting essential posttranslational modification of Wnt reduced tumour growth and markedly decreased the proliferative potential of lung cancer cells, leading to improved survival of tumour-bearing mice. These results indicate that strategies for disrupting pathways that maintain stem-like and niche cell phenotypes can translate into effective anti-cancer therapies.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adenocarcinoma / Progressão da Doença / Proteínas Wnt / Nicho de Células-Tronco / Via de Sinalização Wnt / Neoplasias Pulmonares Limite: Animals / Female / Humans / Male Idioma: En Revista: Nature Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adenocarcinoma / Progressão da Doença / Proteínas Wnt / Nicho de Células-Tronco / Via de Sinalização Wnt / Neoplasias Pulmonares Limite: Animals / Female / Humans / Male Idioma: En Revista: Nature Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos