Laboratory for Cancer Biology, Departments of Medical Oncology and Clinical Research, Cancer Institute (WIA), 38, Sardar Patel Road, Guindy, Chennai, Tamil Nadu, 600036, India.
Amity Institute of Molecular Medicine & Stem Cell Research, Amity University Campus, Sector-125, 201303, Noida, Uttar Pradesh, India.
Cell Oncol (Dordr). 2020 Aug;43(4):601-616. doi: 10.1007/s13402-020-00504-w. Epub 2020 May 8.
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).
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.
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.
已知癌症干细胞(CSCs)的信号转导至少部分通过保守的发育途径发生。在这里,评估了这些途径之一,即 hedgehog 途径,在高级别浆液性卵巢癌(HGSOC)中的作用。
我们发现,在 HGSOC 中,hedgehog 抑制剂(HHIs)GANT61、LDE225 和 GDC0449 减少或抑制了富含 CSCs 的球体的形成。在 HHIs 存在的情况下培养的来自 HGSOC 患者的腹水的原代恶性细胞(PMCs)显示 CSCs 明显减少。Sonic hedgehog(SHH)显着增加了 ALDH1A1 的表达,而 GANT61 则抑制了其表达。在 SHH 中和抗体(5E1)的存在下,观察到源自 HGSOC 的细胞系中的球体数量显着减少。此外,HHIs 显着降低了细胞的运动性、迁移和克隆生长能力。在 GANT61 的存在下,观察到来自 PMCs 的细胞在细胞周期的 G0 期减少。在具有后续随访复发的患者中,来自相同 HGSOC 患者的肿瘤中 Gli1 的表达差异的幅度更大。GANT61 还显着抑制了裸鼠中 CSCs 的生长。最后,用 GANT61 处理的 HGSOC 细胞的 RNA 测序显示 CSC 标志物的表达显着降低。
我们的结果表明 hedgehog 途径在维持 HGSOC 中 CSCs 的完整性方面起着重要作用,可能是一个潜在的治疗靶点。