Fibroblast activation and senescence in oral cancer

被引:27
作者
Prime, S. S. [1 ]
Cirillo, N. [2 ]
Hassona, Y. [3 ]
Lambert, D. W. [4 ]
Paterson, I. C. [5 ]
Mellone, M. [6 ]
Thomas, G. J. [6 ]
James, E. N. L. [1 ]
Parkinson, E. K. [1 ]
机构
[1] Queen Mary Univ London, Inst Dent, Barts & London Sch Med & Dent, Ctr Clin & Diagnost Oral Sci, Turner St, London E1 2AD, England
[2] Univ Melbourne, Melbourne Dent Sch & Oral Hlth CRC, Carlton, Vic, Australia
[3] Univ Jordan, Dept Dent, Amman, Jordan
[4] Univ Sheffield, Sch Clin Dent, Integrat Biosci, Sheffield, S Yorkshire, England
[5] Univ Malaya, Dept Oral Biol & Biomed Sci & Oral Canc Res & Co, Fac Dent, Kuala Lumpur, Malaysia
[6] Univ Southampton, Canc Sci Unit, Fac Med, Southampton, Hants, England
关键词
activation; cancer; fibroblasts; oral; senescence; CARCINOMA-ASSOCIATED FIBROBLASTS; SQUAMOUS-CELL CARCINOMA; MESENCHYMAL TRANSITION; SERUM METABOLOMICS; TUMOR-STROMA; DNA-DAMAGE; TGF-BETA; HEAD; PROGRESSION; CHEMORESISTANCE;
D O I
10.1111/jop.12456
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
There is now compelling evidence that the tumour stroma plays an important role in the pathogenesis of cancers of epithelial origin. The pre-eminent cell type of the stroma is carcinoma-associated fibroblasts. These cells demonstrate remarkable heterogeneity with activation and senescence being common stress responses. In this review, we summarise the part that these cells play in cancer, particularly oral cancer, and present evidence to show that activation and senescence reflect a unified programme of fibroblast differentiation. We report advances concerning the senescent fibroblast metabolome, mechanisms of gene regulation in these cells and ways in which epithelial cell adhesion is dysregulated by the fibroblast secretome. We suggest that the identification of fibroblast stress responses may be a valuable diagnostic tool in the determination of tumour behaviour and patient outcome. Further, the fact that stromal fibroblasts are a genetically stable diploid cell population suggests that they may be ideal therapeutic targets and early work in this context is encouraging.
引用
收藏
页码:82 / 88
页数:7
相关论文
共 59 条
  • [1] p38MAPK Plays a Crucial Role in Stromal-Mediated Tumorigenesis
    Alspach, Elise
    Flanagan, Kevin C.
    Luo, Xianmin
    Ruhland, Megan K.
    Huang, Hui
    Pazolli, Ermira
    Donlin, Maureen J.
    Marsh, Timothy
    Piwnica-Worms, David
    Monahan, Joseph
    Novack, Deborah V.
    McAllister, Sandra S.
    Stewart, Sheila A.
    [J]. CANCER DISCOVERY, 2014, 4 (06) : 716 - 729
  • [2] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [3] CD34+ fibrocytes, α-smooth muscle antigen-positive myofibroblasts, and CD117 expression in the stroma of invasive squamous cell carcinomas of the oral cavity, pharynx, and larynx
    Barth, PJ
    Schweinsberg, TSZ
    Ramaswamy, A
    Moll, R
    [J]. VIRCHOWS ARCHIV, 2004, 444 (03) : 231 - 234
  • [4] The gene expression program of prostate fibroblast senescence modulates neoplastic epithelial cell proliferation through paracrine mechanisms
    Bavik, C
    Coleman, I
    Dean, JP
    Knudsen, B
    Plymate, S
    Nelson, PS
    [J]. CANCER RESEARCH, 2006, 66 (02) : 794 - 802
  • [5] MicroRNAs miR-146a/b negatively modulate the senescence associated inflammatory mediators IL-6 and IL-8
    Bhaumik, Dipa
    Scott, Gary K.
    Schokrpur, Shiruyeh
    Patil, Christopher K.
    Orjalo, Arturo V.
    Rodier, Francis
    Lithgow, Gordon J.
    Campisi, Judith
    [J]. AGING-US, 2009, 1 (04): : 402 - 411
  • [6] Targeting Carcinoma-Associated Fibroblasts Within the Tumor Stroma With a Fibroblast Activation Protein-Activated Prodrug
    Brennen, W. Nathaniel
    Rosen, D. Marc
    Wang, Hao
    Isaacs, John T.
    Denmeade, Samuel R.
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2012, 104 (17): : 1320 - 1334
  • [7] TGF-beta in CAF-mediated tumor growth and metastasis
    Calon, A.
    Tauriello, D. V. F.
    Batlle, E.
    [J]. SEMINARS IN CANCER BIOLOGY, 2014, 25 : 15 - 22
  • [8] Cellular senescence: when bad things happen to good cells
    Campisi, Judith
    di Fagagna, Fabrizio d'Adda
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2007, 8 (09) : 729 - 740
  • [9] Trends in incidence and prognosis for head and neck cancer in the United States: A site-specific analysis of the SEER database
    Carvalho, AL
    Nishimoto, IN
    Califano, JA
    Kowalski, LP
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2005, 114 (05) : 806 - 816
  • [10] Tumor Suppressor and Aging Biomarker p16INK4a Induces Cellular Senescence without the Associated Inflammatory Secretory Phenotype
    Coppe, Jean-Philippe
    Rodier, Francis
    Patil, Christopher K.
    Freund, Adam
    Desprez, Pierre-Yves
    Campisi, Judith
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (42) : 36396 - 36403