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干细胞中的突变定义了头颈癌患者中侵袭性较强的一个亚组,这些患者预后较差、会发生肺转移且治疗失败。

Mutations in Stem Cells Define an Aggressive Subset of Head and Neck Cancer Patients Who Have a Poor Prognosis, Lung Metastasis, and Therapeutic Failure.

作者信息

Islam Syed S, Karakas Bedri, Aboussekhra Abdelilah, Noman Abu Shadat M

机构信息

Department Molecular Oncology, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia.

Faculty of Medicine, Al-Faisal University, Riyadh 11533, Saudi Arabia.

出版信息

Cancers (Basel). 2023 Oct 16;15(20):5006. doi: 10.3390/cancers15205006.

DOI:10.3390/cancers15205006
PMID:37894373
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10605399/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4249/10605399/0a61d358864f/cancers-15-05006-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4249/10605399/4197835e2b0b/cancers-15-05006-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4249/10605399/505bdb6c988e/cancers-15-05006-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4249/10605399/0a61d358864f/cancers-15-05006-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4249/10605399/4197835e2b0b/cancers-15-05006-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4249/10605399/505bdb6c988e/cancers-15-05006-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4249/10605399/0a61d358864f/cancers-15-05006-g003.jpg

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本文引用的文献

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Cell Death Dis. 2022 Aug 9;13(8):696. doi: 10.1038/s41419-022-05126-8.
2
Mutations Predict Lung Cancer Radiation Resistance That Can Be Targeted by Glutaminase Inhibition.突变可预测肺癌放疗抵抗,谷氨酰胺酶抑制可靶向治疗。
Cancer Discov. 2020 Dec;10(12):1826-1841. doi: 10.1158/2159-8290.CD-20-0282. Epub 2020 Oct 18.
3
Chemotherapeutic resistance of head and neck squamous cell carcinoma is mediated by EpCAM induction driven by IL-6/p62 associated Nrf2-antioxidant pathway activation.
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Cell Death Dis. 2020 Aug 20;11(8):663. doi: 10.1038/s41419-020-02907-x.
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Radiation resistance in head and neck squamous cell carcinoma: dire need for an appropriate sensitizer.头颈部鳞状细胞癌的辐射抗性:迫切需要合适的增敏剂。
Oncogene. 2020 Apr;39(18):3638-3649. doi: 10.1038/s41388-020-1250-3. Epub 2020 Mar 10.
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Long-term survival in patients with metastatic head and neck squamous cell carcinoma treated with metastasis-directed therapy.转移性头颈部鳞状细胞癌患者接受转移导向治疗的长期生存。
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