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用于非小细胞肺癌临床前研究的基因组和临床注释患者来源异种移植资源。

A Genomically and Clinically Annotated Patient-Derived Xenograft Resource for Preclinical Research in Non-Small Cell Lung Cancer.

机构信息

The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut.

University of California Davis Comprehensive Cancer Center, Sacramento, California.

出版信息

Cancer Res. 2022 Nov 15;82(22):4126-4138. doi: 10.1158/0008-5472.CAN-22-0948.

Abstract

UNLABELLED

Patient-derived xenograft (PDX) models are an effective preclinical in vivo platform for testing the efficacy of novel drugs and drug combinations for cancer therapeutics. Here we describe a repository of 79 genomically and clinically annotated lung cancer PDXs available from The Jackson Laboratory that have been extensively characterized for histopathologic features, mutational profiles, gene expression, and copy-number aberrations. Most of the PDXs are models of non-small cell lung cancer (NSCLC), including 37 lung adenocarcinoma (LUAD) and 33 lung squamous cell carcinoma (LUSC) models. Other lung cancer models in the repository include four small cell carcinomas, two large cell neuroendocrine carcinomas, two adenosquamous carcinomas, and one pleomorphic carcinoma. Models with both de novo and acquired resistance to targeted therapies with tyrosine kinase inhibitors are available in the collection. The genomic profiles of the LUAD and LUSC PDX models are consistent with those observed in patient tumors from The Cancer Genome Atlas and previously characterized gene expression-based molecular subtypes. Clinically relevant mutations identified in the original patient tumors were confirmed in engrafted PDX tumors. Treatment studies performed in a subset of the models recapitulated the responses expected on the basis of the observed genomic profiles. These models therefore serve as a valuable preclinical platform for translational cancer research.

SIGNIFICANCE

Patient-derived xenografts of lung cancer retain key features observed in the originating patient tumors and show expected responses to treatment with standard-of-care agents, providing experimentally tractable and reproducible models for preclinical investigations.

摘要

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患者来源的异种移植(PDX)模型是一种有效的临床前体内平台,可用于测试癌症治疗新药和药物组合的疗效。在这里,我们描述了一个由 79 个基因组和临床注释的肺癌 PDX 组成的存储库,这些 PDX 来自杰克逊实验室,经过广泛的组织病理学特征、突变谱、基因表达和拷贝数异常分析。大多数 PDX 是非小细胞肺癌(NSCLC)的模型,包括 37 个肺腺癌(LUAD)和 33 个肺鳞癌(LUSC)模型。存储库中的其他肺癌模型包括四个小细胞癌、两个大细胞神经内分泌癌、两个腺鳞癌和一个多形性癌。该集合中还包括具有酪氨酸激酶抑制剂靶向治疗的新发和获得性耐药的模型。LUAD 和 LUSC PDX 模型的基因组谱与癌症基因组图谱中观察到的患者肿瘤和以前基于基因表达的分子亚型一致。在原代患者肿瘤中鉴定的临床相关突变在移植的 PDX 肿瘤中得到了证实。在一部分模型中进行的治疗研究再现了根据观察到的基因组谱预期的反应。因此,这些模型为转化癌症研究提供了有价值的临床前平台。

意义

肺癌的患者来源异种移植保留了起源于患者肿瘤的关键特征,并对标准治疗药物的治疗有预期的反应,为临床前研究提供了可行且可重复的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47cf/9664138/79b2c95ef44c/4126fig1.jpg

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