晚期口腔癌治疗的有效新程序:癌症干细胞检测在指导化疗中的潜力

IF 1.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Translational Medicine at UniSa Pub Date : 2023-12-08 eCollection Date: 2023-01-01 DOI:10.37825/2239-9747.1042
Francesca Spirito, Pier Paolo Claudio, Candace M Howard, Jagan Valluri, Krista L Denning, Lorenzo Lo Muzio, Antonio Cortese
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引用次数: 0

摘要

导言:无效的抗癌疗法会导致不必要的毒性和耐药克隆的产生。许多类型的实体瘤,包括头颈部鳞状细胞癌,都被发现含有一小部分癌症干细胞(CSCs),它们有助于肿瘤的繁殖、维持和抗药性的产生:从原代癌细胞培养物中选择性富集的癌干细胞可用于化疗敏感性测定,以进行功能测试(ChemoID),该测试使用患者的活肿瘤细胞来指示哪种化疗药物(或 "组合")不仅能杀死大部分肿瘤细胞,还能杀死已知会导致癌症复发的癌干细胞。本研究旨在展示从口腔癌患者活检组织中富集的癌干细胞对传统化疗敏感性的测试潜力。本研究纳入了十一名晚期口腔鳞状细胞癌(OSCC)患者的病例系列。我们比较了所有患者的 CSC 检测结果,发现该检测方法预测的化疗反应存在差异:结果:CSC检测发现晚期OSCC患者的化疗反应存在差异,这为肿瘤学家提供了更精确的个性化疗法:OSCC化疗敏感性的变异性表明,有必要在更大的群体中进一步研究该检测方法的使用情况,以便更广泛地了解该临床检测方法的效用。
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A New and Effective Procedure for Advanced Oral Cancer Therapy: The Potential of a Cancer Stem Cell Assay in Guiding Chemotherapy.

Introduction: Ineffective anticancer therapy can result in unnecessary toxicity and the development of resistant clones. Many types of solid tumors, including head and neck squamous cell carcinoma, have been found to contain a small population of cancer stem cells (CSCs) that contribute to tumor propagation, maintenance, and treatment resistance.

Materials and methods: Selectively enriched CSCs from primary cancer cell cultures can be used in a chemosensitivity assay for a functional test (ChemoID) that uses patients' live tumor cells to indicate which chemotherapy agent (or "combinations") will kill not only the bulk of tumor cells but also the CSCs that are known to cause cancer to recur. This study aimed to show the potential of testing the sensitivity of CSCs enriched from oral cancer patients' biopsies to conventional chemotherapies. A case series of eleven patients affected by advanced oral squamous cell carcinoma (OSCC) have been included in this study. We compared the results of the CSC assay among all the patients and found that there was variability in the chemotherapy response predicted by the assay.

Results: Variability in chemotherapy response was found by the CSC assay in advanced OSCC patients suggesting more precise and personalized therapies to the Oncologist.

Conclusions: Variability in chemosensitivity for OSCC warrants the need to investigate further the use of the assay in larger cohorts to gain a broader understanding of the utility of the clinical test.

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Translational Medicine at UniSa
Translational Medicine at UniSa MEDICINE, RESEARCH & EXPERIMENTAL-
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