Abstract |
The tumour microenvironment is a highly heterogeneous entity that plays crucial roles in cancer progression. As the most prominent stromal cell types, cancer-associated fibroblasts (CAFs) produce a variety of factors into the tumour microenvironment. In the present study, we firstly isolated CAFs from tumour tissues of the patients with ovarian cancer and demonstrated that the hepatocyte growth factor (HGF) was highly expressed in the supernatants of CAFs. CAF-derived HGF or human recombinant HGF promoted cell proliferation in human ovarian cell lines SKOV3 and HO-8910 cells. Western blotting analysis also showed that CAF-derived HGF or recombinant HGF activated c-Met/ phosphoinositide 3-kinase (PI3K)/Akt and glucose-regulated protein 78 ( GRP78) signalling pathways in ovarian cancer cells, and these effects could be abrogated by anti-HGF and c-Met inhibitor INCB28060. Moreover, HGF in CAF matrix attenuated paclitaxel (PAC)-caused inhibition of cell proliferation and increase in cell apoptosis through activating c-Met/PI3K/Akt and GRP78 pathways in SKOV3 and HO-8910 cells. The results in vitro were further validated in nude mice. These findings suggest that CAF-derived HGF plays crucial roles in cell proliferation and drug resistance in ovarian cancer cells.
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Authors | Wei Deying, Geng Feng, Liang Shumei, Zhao Hui, Liu Ming, Wang Hongqing |
Journal | Bioscience reports
(Biosci Rep)
Vol. 37
Issue 2
(04 28 2017)
ISSN: 1573-4935 [Electronic] England |
PMID | 28258248
(Publication Type: Journal Article)
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Copyright | © 2017 The Author(s). |
Chemical References |
- Endoplasmic Reticulum Chaperone BiP
- HGF protein, human
- HSPA5 protein, human
- Heat-Shock Proteins
- Hspa5 protein, mouse
- Recombinant Proteins
- Hepatocyte Growth Factor
- Proto-Oncogene Proteins c-met
- Proto-Oncogene Proteins c-akt
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Topics |
- Animals
- Blotting, Western
- Cancer-Associated Fibroblasts
(metabolism)
- Cell Line, Tumor
- Cell Proliferation
(drug effects)
- Drug Resistance, Neoplasm
(drug effects)
- Endoplasmic Reticulum Chaperone BiP
- Female
- Heat-Shock Proteins
(metabolism)
- Hepatocyte Growth Factor
(genetics, metabolism, pharmacology)
- Humans
- Mice, Inbred BALB C
- Mice, Nude
- Microscopy, Fluorescence
- Ovarian Neoplasms
(drug therapy, genetics, metabolism)
- Phosphatidylinositol 3-Kinases
(metabolism)
- Proto-Oncogene Proteins c-akt
(metabolism)
- Proto-Oncogene Proteins c-met
(metabolism)
- Recombinant Proteins
(pharmacology)
- Signal Transduction
(drug effects)
- Up-Regulation
(drug effects)
- Xenograft Model Antitumor Assays
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