The hedgehog pathway regulates cancer stem cells in serous adenocarcinoma of the ovary
Purpose Signaling by cancer stem cells (CSCs) is known to occur at least in part through conserved developmental pathways. Here, the role of one of these pathways, i.e., the hedgehog pathway, was evaluated in high-grade serous ovarian carcinoma (HGSOC). Methods and results We found that in HGSOC, he...
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Veröffentlicht in: | Cellular oncology (Dordrecht) 2020-08, Vol.43 (4), p.601-616 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Purpose
Signaling by cancer stem cells (CSCs) is known to occur at least in part through conserved developmental pathways. Here, the role of one of these pathways, i.e., the
hedgehog
pathway, was evaluated in high-grade serous ovarian carcinoma (HGSOC).
Methods and results
We found that in HGSOC,
hedgehog
inhibitors (HHIs) GANT61, LDE225 and GDC0449 reduced or inhibited the formation of spheroids enriched in CSCs. Primary malignant cells (PMCs) in ascites from HGSOC patients cultured in the presence of HHIs showed significant reduction in CSCs. Sonic hedgehog (SHH) significantly increased the expression of ALDH1A1, which was inhibited by GANT61. In the presence of a SHH neutralizing antibody (5E1), a significant reduction in the number of spheroids was observed in HGSOC-derived cell lines. Further, the motility, migration and clonogenic growth of the cells were significantly reduced by HHIs. In the presence of GANT61, a reduction of cells from PMCs in the G0 phase of the cell cycle was observed. The magnitude of difference in expression of
Gli1
in tumors from the same HGSOC patients at presentation and at interval debulking surgery was greater in patients who had a recurrence on follow up. GANT61 also significantly inhibited the growth of CSCs in nude mice. Finally, RNA sequencing of HGSOC cells treated with GANT61 showed a significantly reduced expression of CSC markers.
Conclusions
Our results indicate that the
hedgehog
pathway plays an important role in maintaining the integrity of CSCs in HGSOC and could be a potential therapeutic target. |
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ISSN: | 2211-3428 2211-3436 |
DOI: | 10.1007/s13402-020-00504-w |