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一种来自rMnSOD前导肽的新型六肽通过雌激素受体进入细胞以递送治疗性分子。

A new hexapeptide from the leader peptide of rMnSOD enters cells through the oestrogen receptor to deliver therapeutic molecules.

作者信息

Borrelli Antonella, Schiattarella Antonietta, Mancini Roberto, Pica Alessandra, Pollio Maria Laura, Ruggiero Maria Grazia, Bonelli Patrizia, De Luca Viviana, Tuccillo Franca Maria, Capasso Clemente, Gori Enrico, Sanseverino Marina, Carpentieri Andrea, Birolo Leila, Pucci Piero, Rommelaere Jean, Mancini Aldo

机构信息

Molecular Biology and Viral Oncology, National Cancer Institute "Fondazione Pascale", Naples, Italy.

Laedhexa Biotechnologies Inc., QB3@953, San Francisco, CA, USA.

出版信息

Sci Rep. 2016 Jan 4;6:18691. doi: 10.1038/srep18691.

Abstract

A 24-amino acid leader peptide of a new human recombinant manganese superoxide dismutase can enter cells and carry molecules. Here, we demonstrated that six of the 24 amino acids penetrate cells through a particular gate represented by a specific amino acid sequence of the oestrogen receptor (ER). We analysed the internalization of the synthetic hexapeptide and the cytotoxic activity of the hexapeptide conjugated to cisplatin on a cell line panel. In most cell lines, the hexapeptide delivered an amount of cisplatin that was 2 to 8 times greater than that released by cisplatin when the drug was used alone. This increased delivery increases the therapeutic index of cisplatin and reduces side effects caused by a high dosage or long-term treatment times. We may consider this hexapeptide a new molecular carrier to deliver molecules with therapeutic activity into ER(+) cells for diagnostic purposes and clinical or immune therapy.

摘要

一种新型人重组锰超氧化物歧化酶的24个氨基酸的前导肽能够进入细胞并携带分子。在此,我们证明了这24个氨基酸中的6个通过由雌激素受体(ER)的特定氨基酸序列所代表的特定通道穿透细胞。我们分析了合成六肽的内化作用以及与顺铂偶联的六肽在一组细胞系上的细胞毒性活性。在大多数细胞系中,该六肽递送的顺铂量比单独使用药物时顺铂释放的量高2至8倍。这种增加的递送提高了顺铂的治疗指数,并减少了高剂量或长期治疗时间所引起的副作用。我们可以将这种六肽视为一种新型分子载体,用于将具有治疗活性的分子递送至ER(+)细胞,以用于诊断目的以及临床或免疫治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a739/4698655/3d0bd75893a4/srep18691-f1.jpg

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