Islam Syed S, Karakas Bedri, Aboussekhra Abdelilah, Noman Abu Shadat M
Department Molecular Oncology, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia.
Faculty of Medicine, Al-Faisal University, Riyadh 11533, Saudi Arabia.
Cancers (Basel). 2023 Oct 16;15(20):5006. doi: 10.3390/cancers15205006.
Mutations in / in head and neck cancer result in abnormal cell growth. Progenitor cells, bulk tumor cells, and head and neck cancer stem cells (HN-CSCs) may all harbor these mutations. Nevertheless, whether mutations in HN-CSCs have an impact on clinical outcomes is unknown. Cancerous HN-CSCs and benign stem cells were obtained from freshly resected head and neck cancer patients (n = 50) via flow cytometry cell sorting and tested for / mutations. The existence of / mutations in HN-CSCs, as well as their correlations with tumor mutations, pathologic tumor stage, tumor histologic grades, lung metastasis, treatment outcomes, and the patient's age and conditions, are assessed at the last follow-up visit. Thirteen tumors were found to have mutations in their HN-CSCs. More than half of the lung metastases and disease progression occurred in HN-CSCs with mutations. Patients whose tumors carried mutations in their HN-CSCs had significantly shorter progression-free survival, overall survival, and time of treatment failure than their non-HN-CSC counterparts. These associations were partly driven by HN-CSCs, in which mutations were overrepresented in fast progressors and associated with an increased risk of disease progression. Our findings suggest that molecular genotyping of HN-CSCs may facilitate personalized treatment strategies and assist in identifying patients who are likely to benefit from chemotherapy.
头颈部癌中的突变会导致细胞异常生长。祖细胞、肿瘤主体细胞以及头颈部癌干细胞(HN-CSCs)可能都携带这些突变。然而,HN-CSCs中的突变是否会影响临床结果尚不清楚。通过流式细胞术细胞分选从刚切除的头颈部癌患者(n = 50)中获取癌性HN-CSCs和良性干细胞,并检测是否存在突变。在最后一次随访时评估HN-CSCs中突变的存在情况,以及它们与肿瘤突变、肿瘤病理分期、肿瘤组织学分级、肺转移、治疗结果以及患者年龄和状况的相关性。发现13个肿瘤的HN-CSCs存在突变。超过一半的肺转移和疾病进展发生在有突变的HN-CSCs中。肿瘤的HN-CSCs携带突变的患者的无进展生存期、总生存期和治疗失败时间明显短于非HN-CSC对应患者。这些关联部分是由HN-CSCs驱动的,其中突变在快速进展者中过度代表,并与疾病进展风险增加相关。我们的研究结果表明,HN-CSCs的分子基因分型可能有助于制定个性化治疗策略,并有助于确定可能从化疗中受益的患者。