Yang Zejia, Liao Jipei, Lapidus Rena G, Fan Xiaoxuan, Mehra Ranee, Cullen Kevin J, Dan Hancai
University of Maryland Greenebaum Comprehensive Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA.
Department of Pathology, University of Maryland School of Medicine, Baltimore, MD, USA.
Cancer Chemother Pharmacol. 2022 Apr;89(4):469-478. doi: 10.1007/s00280-022-04410-w. Epub 2022 Feb 25.
We investigated the role of Wee1 kinase in cisplatin-resistant head and neck squamous cell carcinoma (HNSCC) in multiple cisplatin-resistant HNSCC cell lines and determined the efficacy of either Wee1 inhibitor, AZD1775 alone, or in combination with cisplatin, on cisplatin-resistant HNSCC inhibition.
Phosphorylation and total protein levels of cells were assessed by Western blot analysis. Cell viability and apoptosis were examined by MTS assay and flow cytometry, respectively.
Wee1 kinase protein expression levels in five cisplatin-resistant HNSCC cell types were higher than those in their parental cisplatin-sensitive partners. Importantly, Wee1 knockdown inhibited cell proliferation and re-sensitized cells to cisplatin treatment. Interestingly, previous studies have also shown that Wee1 inhibitor AZD1775 synergizes with cisplatin to suppress cell proliferation of cisplatin-sensitive HNSCC. We found that AZD1775 inhibited both cisplatin-sensitive and resistant HNSCC with similar IC values, which suggested that AZD1775 could overcome cisplatin resistance in cisplatin-resistant HNSCC. Mechanistically, AZD1775 and cisplatin cooperatively induced DNA damage and apoptosis.
Wee1 inhibitor, AZD1775, and cisplatin coordinately suppressed proliferation and survival of HNSCC.
我们在多个顺铂耐药的头颈部鳞状细胞癌(HNSCC)细胞系中研究了Wee1激酶在顺铂耐药HNSCC中的作用,并确定了Wee1抑制剂AZD1775单独使用或与顺铂联合使用对顺铂耐药HNSCC抑制的疗效。
通过蛋白质免疫印迹分析评估细胞的磷酸化和总蛋白水平。分别通过MTS法和流式细胞术检测细胞活力和凋亡情况。
五种顺铂耐药HNSCC细胞类型中Wee1激酶蛋白表达水平高于其亲本顺铂敏感细胞。重要的是,敲低Wee1可抑制细胞增殖并使细胞对顺铂治疗重新敏感。有趣的是,先前的研究还表明,Wee1抑制剂AZD1775与顺铂协同作用可抑制顺铂敏感HNSCC的细胞增殖。我们发现AZD1775以相似的IC值抑制顺铂敏感和耐药的HNSCC,这表明AZD1775可克服顺铂耐药HNSCC中的顺铂耐药性。从机制上讲,AZD1775和顺铂协同诱导DNA损伤和凋亡。
Wee1抑制剂AZD1775和顺铂协同抑制HNSCC的增殖和存活。