Vasilescu Maria M, Panait Marieta E, Dumitru Mirela
Department of Cancer Biochemistry and Radiobiology, Institutul Oncologic Prof. Dr. Alexandru Trestioreanu, Bucharest, ROU.
Department of Cancer Biology, Institutul Oncologic Prof. Dr. Alexandru Trestioreanu, Bucharest, ROU.
Cureus. 2024 Dec 22;16(12):e76208. doi: 10.7759/cureus.76208. eCollection 2024 Dec.
Malignant pleural effusion (MPE) is a common feature in patients with advanced or metastatic malignancies. While significant progress has been made in understanding the biology of pleural effusions, further research is needed to uncover the subsequent behavior of tumor cells following their invasion into the pleural space. This report utilizes flow cytometry to analyze DNA content abnormalities (aneuploidy) and cell cycle status, shedding light on the tumor cell populations present in MPE samples from a patient with lung adenocarcinoma during treatment. The findings suggest that under selective pressure, certain tumor cell subpopulations within the pleural effusion were suppressed, while therapy-resistant subpopulations emerged, driving disease progression. MPE serves as a valuable model for studying tumor heterogeneity and clonal dynamics in real time, offering insights that may inform diagnosis, prognosis, and therapeutic strategies.
恶性胸腔积液(MPE)是晚期或转移性恶性肿瘤患者的常见特征。虽然在理解胸腔积液生物学方面已取得重大进展,但仍需进一步研究以揭示肿瘤细胞侵入胸腔后的后续行为。本报告利用流式细胞术分析DNA含量异常(非整倍体)和细胞周期状态,以阐明一名肺腺癌患者治疗期间MPE样本中存在的肿瘤细胞群体。研究结果表明,在选择性压力下,胸腔积液中的某些肿瘤细胞亚群受到抑制,而出现了抗治疗亚群,推动疾病进展。MPE作为实时研究肿瘤异质性和克隆动态的宝贵模型,可为诊断、预后和治疗策略提供见解。