Free-floating patient-derived organotypic tumor spheroids (PDOTS) from non-small cell lung cancer (NSCLC) tumors: a versatile tool for personalized testing of chemotherapeutic drugs.

IF 2.3 Q3 CHEMISTRY, MEDICINAL
Research in Pharmaceutical Sciences Pub Date : 2025-10-20 eCollection Date: 2025-10-01 DOI:10.4103/RPS.RPS_233_24
Lilian Ismail, Komal Zahid, Anna Polyanskaya, Aya Al Othman, Ningfei Shen, Xiaoli Qi, Rushan Sulimanov, Yuri Esakov, Vladimir Makarov, Gleb Filkov, Alexander Trofimenko, Alexandre Mezentsev, Mikhail Durymanov
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引用次数: 0

Abstract

Background and purpose: Patient-derived tumor 3D multicellular cultures are a novel non-small cell lung cancer (NSCLC) model for studying tumor biology and precision medicine, which recapitulates tumor morphology and gene expression profile. However, practical application is challenged by issues such as low establishment rates, long-term production difficulties, and the absence of immune microenvironment components. To address these issues, this study aimed to evaluate the efficacy of a novel method for generating free-floating patient-derived organotypic tumor spheroids (PDOTS) using a stimuli-responsive extracellular matrix (ECM)-mimicking gel.

Experimental approach: Free-floating PDOTS were established from 18 NSCLC tumors and characterized by their morphology, marker expression, and extracellular matrix composition. Cell composition in PDOTS and their parental tumors was analyzed by flow cytometry, while RT-PCR was used to assess the expression of genes encoding signaling molecules. Finally, drug response and the expression of drug resistance genes were evaluated in the NSCLC PDOTS.

Findings/results: The PDOTS were successfully generated with a success rate exceeding 90%, forming spheroids within one week. These PDOTS preserved the parental tumor's morphology and included stromal and immune cells. Notably, 58% of the PDOTS maintained cytokine and growth factor expression profiles closely mimicked those of the original tumors. Furthermore, the PDOTS demonstrated varied responses to anticancer drugs, potentially influenced by differential expression of drug resistance-associated genes.

Conclusion and implications: The high establishment rate and rapid production timeline of free-floating PDOTS using a stimuli-responsive ECM-mimicking gel make this approach a promising tool for advancing cancer biology research and evaluating therapeutic strategies with greater accuracy.

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来自非小细胞肺癌(NSCLC)肿瘤的自由漂浮患者源性器官型肿瘤球体(PDOTS):一种用于化疗药物个性化测试的多功能工具。
背景与目的:患者源性肿瘤三维多细胞培养是研究肿瘤生物学和精准医学的一种新型非小细胞肺癌(NSCLC)模型,它概括了肿瘤形态和基因表达谱。然而,实际应用受到诸如建立率低、长期生产困难和缺乏免疫微环境成分等问题的挑战。为了解决这些问题,本研究旨在评估一种使用刺激反应性细胞外基质(ECM)模拟凝胶生成自由漂浮的患者源性器官型肿瘤球体(PDOTS)的新方法的有效性。实验方法:从18个非小细胞肺癌肿瘤中建立自由漂浮的PDOTS,并通过其形态、标志物表达和细胞外基质组成进行表征。流式细胞术分析PDOTS及其亲本肿瘤的细胞组成,RT-PCR检测编码信号分子的基因表达。最后,评估NSCLC PDOTS的药物反应和耐药基因的表达。结果:PDOTS成功生成,成功率超过90%,一周内形成球状体。这些PDOTS保留了亲代肿瘤的形态,包括基质细胞和免疫细胞。值得注意的是,58%的PDOTS维持了细胞因子和生长因子的表达谱,与原始肿瘤的表达谱非常相似。此外,PDOTS对抗癌药物表现出不同的反应,可能受到耐药相关基因差异表达的影响。结论和意义:使用刺激反应性ecm模拟凝胶制备自由漂浮PDOTS的高建立率和快速生产时间使该方法成为推进癌症生物学研究和更准确评估治疗策略的有前途的工具。
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来源期刊
Research in Pharmaceutical Sciences
Research in Pharmaceutical Sciences CHEMISTRY, MEDICINAL-
CiteScore
3.60
自引率
19.00%
发文量
50
审稿时长
34 weeks
期刊介绍: Research in Pharmaceutical Sciences (RPS) is included in Thomson Reuters ESCI Web of Science (searchable at WoS master journal list), indexed with PubMed and PubMed Central and abstracted in the Elsevier Bibliographic Databases. Databases include Scopus, EMBASE, EMCare, EMBiology and Elsevier BIOBASE. It is also indexed in several specialized databases including Scientific Information Database (SID), Google Scholar, Iran Medex, Magiran, Index Copernicus (IC) and Islamic World Science Citation Center (ISC).
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