Yaghoubi Naei Vahid, Ivanova Ekaterina, Mullally William, O'Leary Connor G, Ladwa Rahul, O'Byrne Ken, Warkiani Majid E, Kulasinghe Arutha
School of Biomedical Engineering University of Technology Sydney Sydney NSW Australia.
Frazer Institute, Faculty of Medicine The University of Queensland Brisbane QLD Australia.
Clin Transl Immunology. 2024 Jun 3;13(6):e1516. doi: 10.1002/cti2.1516. eCollection 2024.
Globally, non-small cell lung cancer (NSCLC) is the most prevalent form of lung cancer and the leading cause of cancer-related deaths. Tumor-associated circulating cells in NSCLC can have a wide variety of morphological and phenotypic characteristics, including epithelial, immunological or hybrid subtypes. The distinctive characteristics and potential clinical significance of these cells in patients with NSCLC are explored in this study.
We utilised a spiral microfluidic device to enrich large cells and cell aggregates from the peripheral blood samples of NSCLC patients. These cells were characterised through high-resolution immunofluorescent imaging and statistical analysis, correlating findings with clinical information from our patient cohort.
We have identified varied populations of heterotypic circulating tumor cell clusters with differing immune cell composition that included a distinct class of atypical tumor-associated macrophages that exhibits unique morphology and cell size. This subtype's prevalence is positively correlated with the tumor stage, progression and metastasis.
Our study reveals a heterogeneous landscape of circulating tumor cells and their clusters, underscoring the complexity of NSCLC pathobiology. The identification of a unique subtype of atypical tumor-associatedmacrophages that simultaneously express both tumor and immune markers and whose presence correlates with late disease stages, poor clinical outcomes and metastatic risk infers the potential of these cells as biomarkers for NSCLC staging and prognosis. Future studies should focus on the role of these cells in the tumor microenvironment and their potential as therapeutic targets. Additionally, longitudinal studies tracking these cell types through disease progression could provide further insights into their roles in NSCLC evolution and response to treatment.
在全球范围内,非小细胞肺癌(NSCLC)是最常见的肺癌形式,也是癌症相关死亡的主要原因。NSCLC中与肿瘤相关的循环细胞可具有多种形态和表型特征,包括上皮、免疫或混合亚型。本研究探讨了这些细胞在NSCLC患者中的独特特征和潜在临床意义。
我们利用螺旋微流控装置从NSCLC患者的外周血样本中富集大细胞和细胞聚集体。通过高分辨率免疫荧光成像和统计分析对这些细胞进行表征,并将结果与我们患者队列的临床信息相关联。
我们鉴定出了具有不同免疫细胞组成的多种异型循环肿瘤细胞簇群体,其中包括一类独特的非典型肿瘤相关巨噬细胞,其表现出独特的形态和细胞大小。这种亚型的患病率与肿瘤分期、进展和转移呈正相关。
我们的研究揭示了循环肿瘤细胞及其簇的异质性景观,突显了NSCLC病理生物学的复杂性。鉴定出一种独特的非典型肿瘤相关巨噬细胞亚型,其同时表达肿瘤和免疫标志物,且其存在与疾病晚期、不良临床结局和转移风险相关,这表明这些细胞作为NSCLC分期和预后生物标志物的潜力。未来的研究应关注这些细胞在肿瘤微环境中的作用及其作为治疗靶点的潜力。此外,通过疾病进展追踪这些细胞类型的纵向研究可以进一步深入了解它们在NSCLC演变和治疗反应中的作用。