Literature DB >> 28462708

Collaborative and Defensive Fibroblasts in Tumor Progression and Therapy Resistance.

Barbara Chiavarina1, Andrei Turtoi2.   

Abstract

Tumor microenvironment is a complex network of epithelial cancer cells and non-transformed stromal cells. Of the many stromal cell types, fibroblasts are the most numerous ones and are traditionally viewed as supportive elements of cancer progression. Many studies show that cancer cells engage in active crosstalk with associated fibroblasts in order to obtain key resources, such as growth factors and nutrients. The facets of fibroblast "complicity to murder" in cancer are multiple. However, recent therapeutic attempts aiming at depleting fibroblasts from tumors, perturbed rather simplistic picture. Contrary to the expectations, tumors devoid of fibroblasts accelerated their progression while patients faced poorer outcomes. These studies remind us of the physiologic roles fibroblasts have in maintaining tissue homeostasis even in the presence of cancer. It is becoming increasingly clear that our research focus on advanced tumors has biased our understanding of fibroblast role in tumor biology. The numerous events where the fibroblasts protect the tissue from malignant transformation remain largely unacknowledged, as the tumors are invisible. The present review has the ambition to offer a more balanced view of fibroblasts functions in cancer progression and therapy resistance. We will address the question whether it is possible to synergize the efforts with fibroblasts as the therapeutic concept against tumor progression and therapy resistance. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

Entities:  

Keywords:  CAF; TGF-β1; heterogeneity; metastasis; microenvironment; pancreatic cancer

Mesh:

Substances:

Year:  2017        PMID: 28462708     DOI: 10.2174/0929867324666170428104311

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  3 in total

1.  Fibroblast-derived prolargin is a tumor suppressor in hepatocellular carcinoma.

Authors:  Masahiko Nishiyama; Andrei Turtoi; Barbara Chiavarina; Roberto Ronca; Yukihiro Otaka; Roger Bryan Sutton; Sara Rezzola; Takehiko Yokobori; Paola Chiodelli; Regis Souche; Didier Pourquier; Antonio Maraver; Gavino Faa; Lakhdar Khellaf; Evgenia Turtoi; Tetsunari Oyama; Stephanie Gofflot; Akeila Bellahcène; Olivier Detry; Philippe Delvenne; Vincent Castronovo
Journal:  Oncogene       Date:  2022-01-14       Impact factor: 8.756

2.  Tspan8-Tumor Extracellular Vesicle-Induced Endothelial Cell and Fibroblast Remodeling Relies on the Target Cell-Selective Response.

Authors:  Wei Mu; Jan Provaznik; Thilo Hackert; Margot Zöller
Journal:  Cells       Date:  2020-01-29       Impact factor: 6.600

3.  Single-Cell RNA Sequencing Unravels Heterogeneity of the Stromal Niche in Cutaneous Melanoma Heterogeneous Spheroids.

Authors:  Jiří Novotný; Karolína Strnadová; Barbora Dvořánková; Šárka Kocourková; Radek Jakša; Pavel Dundr; Václav Pačes; Karel Smetana; Michal Kolář; Lukáš Lacina
Journal:  Cancers (Basel)       Date:  2020-11-10       Impact factor: 6.639

  3 in total

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