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BRCA 缺陷型小鼠乳腺肿瘤类器官用于研究癌症耐药性。

BRCA-deficient mouse mammary tumor organoids to study cancer-drug resistance.

机构信息

Division of Molecular Pathology and Cancer Genomics Netherlands, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Hubrecht Institute for Developmental Biology and Stem Cell Research, University Medical Centre Utrecht, Utrecht, The Netherlands.

出版信息

Nat Methods. 2018 Feb;15(2):134-140. doi: 10.1038/nmeth.4535. Epub 2017 Dec 11.

Abstract

Poly(ADP-ribose) polymerase inhibition (PARPi) is a promising new therapeutic approach for the treatment of cancers that show homologous recombination deficiency (HRD). Despite the success of PARPi in targeting HRD in tumors that lack the tumor suppressor function of BRCA1 or BRCA2, drug resistance poses a major obstacle. We developed three-dimensional cancer organoids derived from genetically engineered mouse models (GEMMs) for BRCA1- and BRCA2-deficient cancers. Unlike conventional cell lines or mammospheres, organoid cultures can be efficiently derived and rapidly expanded in vitro. Orthotopically transplanted organoids give rise to mammary tumors that recapitulate the epithelial morphology and preserve the drug response of the original tumor. Notably, GEMM-tumor-derived organoids can be easily genetically modified, making them a powerful tool for genetic studies of tumor biology and drug resistance.

摘要

聚(ADP-核糖)聚合酶抑制(PARPi)是治疗同源重组缺陷(HRD)癌症的一种很有前途的新治疗方法。尽管 PARPi 在针对缺乏 BRCA1 或 BRCA2 肿瘤抑制功能的 HRD 肿瘤方面取得了成功,但耐药性仍是一个主要障碍。我们开发了源自基因工程小鼠模型(GEMM)的 BRCA1 和 BRCA2 缺陷型癌症的三维癌症类器官。与传统细胞系或乳腺球体不同,类器官培养物可以在体外高效地衍生和快速扩增。原位移植的类器官产生的乳腺肿瘤再现了上皮形态,并保留了原始肿瘤的药物反应。值得注意的是,GEMM-肿瘤衍生的类器官可以很容易地进行基因修饰,使它们成为肿瘤生物学和耐药性遗传研究的有力工具。

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