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      TGF-beta in CAF-mediated tumor growth and metastasis.

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          Abstract

          TGF-beta signaling is one of the major pathways controlling cell and tissue behavior not only in homeostasis but also in disease. During tumorigenesis TGF-beta orchestrated processes are key due to its dual role as tumor suppressor and tumor promoter. Important functions of this pathway have been described in a context-dependent manner both in epithelial cancer cells and in the tumor microenvironment during tumor progression. Carcinoma-associated fibroblasts (CAFs) are one of the most abundant stromal cell types in virtually all solid tumors. CAFs favor malignant progression by providing cancer cells with proliferative, migratory, survival and invasive capacities. A complex network of signaling pathways underlying their tumor-promoting properties is beginning to take shape. In this review, we examine current evidence on the emerging mechanisms involving TGF-beta in CAF-mediated cancer progression, and discuss their potential as therapeutic targets.

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          Author and article information

          Journal
          Semin. Cancer Biol.
          Seminars in cancer biology
          1096-3650
          1044-579X
          Apr 2014
          : 25
          Affiliations
          [1 ] Oncology Department, Institute for Research in Biomedicine, 08028 Barcelona, Spain. Electronic address: alexandre.calon@irbbarcelona.org.
          [2 ] Oncology Department, Institute for Research in Biomedicine, 08028 Barcelona, Spain.
          [3 ] Oncology Department, Institute for Research in Biomedicine, 08028 Barcelona, Spain; Institució Catalana de Recerca i Estudis Avançats (ICREA), 08010 Barcelona, Spain. Electronic address: eduard.batlle@irbbarcelona.org.
          Article
          S1044-579X(14)00005-4
          10.1016/j.semcancer.2013.12.008
          24412104
          c4717a30-76e2-4a4f-befd-6bf490e39724
          Copyright © 2014 Elsevier Ltd. All rights reserved.
          History

          Cancer-associated fibroblast,Metastasis,Stroma,TGF-beta,Tumor microenvironment

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