Fibroblast EXT1-Levels Influence Tumor Cell Proliferation and Migration in Composite Spheroids

被引:22
作者
Osterholm, Cecilia [1 ]
Lu, Ning [1 ]
Liden, Asa [1 ]
Karlsen, Tine V. [1 ]
Gullberg, Donald [1 ]
Reed, Rolf K. [1 ]
Kusche-Gullberg, Marion [1 ]
机构
[1] Univ Bergen, Dept Biomed, Bergen, Norway
来源
PLOS ONE | 2012年 / 7卷 / 07期
关键词
INTERSTITIAL FLUID PRESSURE; HEPARAN-SULFATE; EXTRACELLULAR-MATRIX; CANCER; INTEGRIN; STROMA; PROTEOGLYCANS; SYNDECAN-1; ACTIVATION; GROWTH;
D O I
10.1371/journal.pone.0041334
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Stromal fibroblasts are important determinants of tumor cell behavior. They act to condition the tumor microenvironment, influence tumor growth, support tumor angiogenesis and affect tumor metastasis. Heparan sulfate proteoglycans, present both on tumor and stromal cells, interact with a large number of ligands including growth factors, their receptors, and structural components of the extracellular matrix. Being ubiquitously expressed in the tumor microenvironment heparan sulfate proteoglycans are candidates for playing central roles in tumor-stroma interactions. The objective of this work was to investigate the role of heparan sulfate expressed by stromal fibroblasts in modulating the growth of tumor cells and in controlling the interstitial fluid pressure in a 3-D model. Methodology/Principal Findings: We generated spheroids composed of fibroblasts alone, or composite spheroids, composed of fibroblasts and tumor cells. Here we show that stromal fibroblasts with a mutation in the heparan sulfate elongating enzyme Ext1 and thus a low heparan sulfate content, formed composite fibroblast/tumor cell spheroids with a significant lower interstitial fluid pressure than corresponding wild-type fibroblast/tumor cell composite spheroids. Furthermore, immunohistochemistry of composite spheroids revealed that the cells segregated, so that after 6 days in culture, the wild-type fibroblasts formed an inner core and the tumor cells an outer layer of cells. For composite spheroids containing Ext1-mutated fibroblasts this segregation was less obvious, indicating impaired cell migration. Analysis of tumor cells expressing the firefly luciferase gene revealed that the changes in tumor cell migration in mutant fibroblast/tumor cell composite spheroids coincided with a lower proliferation rate. Conclusions/Significance: This is the first demonstration that stromal Ext1-levels modulate tumor cell proliferation and affect the interstitial fluid pressure in a 3-D spheroid model. Learning how structural changes in stromal heparan sulfate influence tumor cells is essential for our understanding how non-malignant cells of the tumor microenvironment influence tumor cell progression.
引用
收藏
页数:10
相关论文
共 50 条
  • [31] Hedgehog pathway regulators influence cervical cancer cell proliferation, survival and migration
    Samarzija, Ivana
    Beard, Peter
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2012, 425 (01) : 64 - 69
  • [32] LncRNA FEZF1-AS1 aggravates cell proliferation and migration in glioblastoma
    Zhou, Chaoyang
    Jiang, Xingxing
    Liang, Aijun
    Zhu, Ronglan
    Yang, Yu
    Zhong, Liangchen
    Wan, Dengfeng
    NEUROSCIENCE LETTERS, 2021, 764
  • [33] Lentivirus-Mediated Knockdown of CTHRC1 Inhibits Osteosarcoma Cell Proliferation and Migration
    Sang, Weilin
    Zhu, Libo
    Ma, Jinzhong
    Lu, Haiming
    Wang, Cong
    CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS, 2016, 31 (03) : 91 - 98
  • [34] β1 integrin mediates colorectal cancer cell proliferation and migration through regulation of the Hedgehog pathway
    Song, Jia
    Zhang, Jixiang
    Wang, Jing
    Wang, Jun
    Guo, Xufeng
    Dong, Weiguo
    TUMOR BIOLOGY, 2015, 36 (03) : 2013 - 2021
  • [35] Effects of human Dachshund homolog 1 on the proliferation, migration, and adhesion of squamous cell carcinoma of the tongue
    Zhang, Li
    Wang, Cheng-Qin
    Liu, Fen
    Dong, Zuo-Qing
    Zhao, Peng
    Dong, Xian-ning
    Wei, Fengcai
    Qu, Xun
    Xiang, Feng-Gang
    ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY, 2016, 121 (01): : 58 - 66
  • [36] miR-934 as a Prognostic Marker Facilitates Cell Proliferation and Migration of Pancreatic Tumor by Targeting PROX1
    Jin, Yangbing
    Weng, Yuanchi
    Wang, Yue
    Lin, Jiewei
    Deng, Xiaxing
    Shen, Baiyong
    Zhan, Qian
    Lu, Xiongxiong
    ONCOTARGETS AND THERAPY, 2020, 13 : 3389 - 3399
  • [37] PKD1 negatively regulates cell invasion, migration and proliferation ability of human osteosarcoma
    Onishi, Yasuo
    Kawamoto, Teruya
    Kishimoto, Kenta
    Hara, Hitomi
    Fukase, Naomasa
    Toda, Mitsunori
    Harada, Risa
    Kurosaka, Masahiro
    Akisue, Toshihiro
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2012, 40 (06) : 1839 - 1848
  • [38] Blocking of stromal interaction molecule 1 expression influence cell proliferation and promote cell apoptosis in vitro and inhibit tumor growth in vivo in head and neck squamous cell carcinoma
    Li, Ping
    Bian, Xue-yan
    Chen, Qing
    Yao, Xiao-feng
    Wang, Xu-dong
    Zhang, Wen-chao
    Tao, Ying-jie
    Jin, Rui
    Zhang, Lun
    PLOS ONE, 2017, 12 (05):
  • [39] Effectiveness of tumor-treating fields to reduce the proliferation and migration of liposarcoma cell lines
    Lee, Won Seok
    Jang, Yoonjung
    Cho, Ahyeon
    Kim, Yu Bin
    Bu, Young Hyun
    Yang, Somi
    Kim, Eun Ho
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2023, 26 (02)
  • [40] Synthesis and investigation of the Role of Benzopyran Dihydropyrimidinone Hybrids in Cell Proliferation, Migration and Tumor Growth
    Dash, Ashutosh K.
    Nayak, Debasis
    Hussain, Nazar
    Mintoo, Mubashir J.
    Bano, Sumera
    Katoch, Archana
    Mondhe, Dilip M.
    Goswami, Anindya
    Mukherjee, Debaraj
    ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2019, 19 (02) : 276 - 288