Tumor-associated mesenchymal stem-like cells provide extracellular signaling cue for invasiveness of glioblastoma cells
- Authors
- Lim, Eun-Jung; Suh, Yongjoon; Yoo, Ki-Chun; Lee, Ji-Hyun; Kim, In-Gyu; Kim, Min-Jung; Chang, Jong Hee; Kang, Seok-Gu; Lee, Su-Jae
- Issue Date
- Jan-2017
- Publisher
- Impact Journals
- Keywords
- extracellular matrix remodeling; mesenchymal stem-like cells; hyaluronic acid; hyaluronic acid synthase-2; C5a
- Citation
- Oncotarget, v.8, no.1, pp 1438 - 1448
- Pages
- 11
- Indexed
- SCIE
SCOPUS
- Journal Title
- Oncotarget
- Volume
- 8
- Number
- 1
- Start Page
- 1438
- End Page
- 1448
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/21248
- DOI
- 10.18632/oncotarget.13638
- ISSN
- 1949-2553
1949-2553
- Abstract
- Hyaluronic acid (HA) is abundant in tumor microenvironment and closely associated with invasiveness of glioblastoma (GM) cells. However, the cellular mechanism underlying HA-rich microenvironment in GBM remains unexplored. Here, we show that tumor-associated mesenchymal stem-like cells (tMSLCs) contribute to abundance of hyaluronic acid (HA) in tumor microenvironment through HA synthase-2 (HAS2) induction, and thereby enhances invasiveness of GBM cells. In an autocrine manner, C5a secreted by tMSLCs activated ERK MAPK for HAS2 induction in tMSLCs. Importantly, HA acted as a signaling ligand of its cognate receptor RHAMM for intracellular signaling activation underlying invasiveness of GBM cells. Taken together, our study suggests that tMSLCs contribute to HA-rich proinvasive ECM microenvironment in GBM.
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