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线粒体携带有突变 DNA 通过细胞外囊泡运动有助于癌细胞获得化疗耐药性。

Movement of Mitochondria with Mutant DNA through Extracellular Vesicles Helps Cancer Cells Acquire Chemoresistance.

机构信息

Department of Experimental and Health Sciences, Universitat Pompeu Fabra, Doctor Aiguader 88, 08003, Barcelona, Spain.

Faculty of Engineering and Natural Sciences, Sabancı University, Istanbul, 34956, Turkey.

出版信息

ChemMedChem. 2022 Feb 16;17(4):e202100642. doi: 10.1002/cmdc.202100642. Epub 2021 Dec 9.

Abstract

Triple negative breast cancer (TNBC) is one of the most aggressive subtypes of breast cancer with the worst prognosis after chemo- or radiation therapy. This is mainly due to the development of cancer chemoresistance accompanied by tumor recurrence. In this work, we investigated a new mechanism of acquired chemoresistance of TNBC cells. We showed that extracellular vehicles (EVs) of chemoresistant TNBC cells can transfer mitochondria to sensitive cancer cells, thus increasing their chemoresistance. Such transfer, but with less efficiency, can be carried out over short distances using tunneling nanotubes. In addition, we showed that exosome fractions carrying mitochondria from resistant TNBC cells contribute to acquired chemoresistance by increasing mtDNA levels with mutations in the mtND4 gene responsible for tumorigenesis. Blocking mitochondrial transport by exosome inhibitors, including GW4869, reduced acquired TNBC chemoresistance. These results could lead to the identification of new molecular targets necessary for more effective treatment of this type of cancer.

摘要

三阴性乳腺癌(TNBC)是乳腺癌中侵袭性最强的亚型之一,在化疗或放疗后预后最差。这主要是由于癌症耐药性的发展伴随着肿瘤复发。在这项工作中,我们研究了 TNBC 细胞获得性化疗耐药的新机制。我们表明,耐药 TNBC 细胞的细胞外囊泡(EVs)可以将线粒体转移到敏感的癌细胞中,从而增加其化疗耐药性。这种转移,但效率较低,可以通过使用隧道纳米管在短距离内进行。此外,我们还表明,来自耐药 TNBC 细胞的携带线粒体的外体部分通过增加 mtDNA 水平并导致肿瘤发生的 mtND4 基因突变,导致获得性化疗耐药。用外体抑制剂(包括 GW4869)阻断线粒体运输,可降低 TNBC 的获得性化疗耐药性。这些结果可能导致确定新的分子靶点,从而更有效地治疗这种类型的癌症。

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