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纳米载环状单链 DNA 使共沉默的肿瘤抑制基因去抑制可降低肿瘤恶性程度。

Derepression of co-silenced tumor suppressor genes by nanoparticle-loaded circular ssDNA reduces tumor malignancy.

机构信息

State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China.

Tianjin Key Laboratory of Molecular Drug Research, Tianjin International Joint Academy of Biomedicine, Tianjin, China.

出版信息

Sci Transl Med. 2018 May 23;10(442). doi: 10.1126/scitranslmed.aao6321.

Abstract

The co-silencing of multiple tumor suppressor genes can lead to escalated malignancy in cancer cells. Given the limited efficacy of anticancer therapies targeting single tumor suppressor genes, we developed small circular single-stranded DNA (CSSD) that can up-regulate the expression of co-silenced tumor suppressor genes by sequestering microRNAs (miRNAs) that negatively regulate these genes. We found that cancer patients with low tumor expression of the tumor suppressor genes , , and had shortened survival times. The up-regulation of these genes upon transfection of artificial CSSD-9 inhibited tumor proliferation and metastasis and promoted apoptosis in vitro as well as in ex vivo and patient-derived xenograft models. In addition, CSSD is more stable and effective than current miRNA inhibitors, and transfecting CSSDs via nanoparticles substantially improved delivery efficiency. The use of a single CSSD can promote the inhibition of multiple tumor suppressor genes. This study provides evidence for the possibility of using CSSDs as therapeutic miRNA inhibitors to target the co-silencing of multiple tumor suppressor genes.

摘要

多个肿瘤抑制基因的共沉默会导致癌细胞恶性程度的加剧。鉴于针对单个肿瘤抑制基因的抗癌疗法效果有限,我们开发了一种小环状单链 DNA(CSSD),它可以通过隔离负调控这些基因的 microRNA(miRNA)来上调共沉默的肿瘤抑制基因的表达。我们发现,肿瘤抑制基因 、 、 在肿瘤中低表达的癌症患者的生存时间较短。人工 CSSD-9 转染后这些基因的上调抑制了肿瘤的增殖和转移,并促进了体外以及离体和患者来源的异种移植模型中的细胞凋亡。此外,CSSD 比目前的 miRNA 抑制剂更稳定、更有效,并且通过纳米粒转染 CSSD 大大提高了递送效率。使用单个 CSSD 可以促进多个肿瘤抑制基因的抑制。这项研究为使用 CSSD 作为治疗性 miRNA 抑制剂来靶向多个肿瘤抑制基因的共沉默提供了证据。

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