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[一种基于慢病毒的改良报告基因用于癌症干细胞的磁性分离]

[A Modified Lentivirus-Based Reporter for Magnetic Separation of Cancer Stem Cells].

作者信息

Ivanova A E, Kravchenko D S, Chumakov S P

机构信息

Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, 117997 Russia.

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, 119991 Russia.

出版信息

Mol Biol (Mosk). 2020 Jan-Feb;54(1):95-102. doi: 10.31857/S0026898419040049.

Abstract

Cancer stem cells (CSCs) are the most malignant subpopulation of tumor cells that possess a tumorigenic potential and resistantance to chemotherapy. These properties make CSCs a promising target for the development of targeted antitumor therapy which is especially in demand in highly aggressive cancers. However, the correct identification of cancer cells with stem properties remains a challenge. A newly developed lentivirus-based reporter SORE6 allows to directly identify CSCs by measuring gene expression of the embryonic stem cell factors SOX2 and OCT4. In the current study the reporter was modified to enable isolation of SOX2^(+)/OCT4^(+) cells by immunomagnetic separation and then was used to transduce HCC1806 and MDA-MB-453 triple-negative breast cancer (TNBC) cell lines. To validate the modified reporter, SOX2^(+)/OCT4^(+) populations were isolated and analyzed for the content of NANOG, a key transcription factor of pluropotency which expression is regulated by SOX2/OCT4. The percentage of SOX2^(+)/OCT4^(+) cells was assessed for each cell line. An increased content of NANOG protein was found in isolated SOX2^(+)/OCT4^(+) cell fractions indicating that the modified reporter is suitable for further studying the CSC subset.

摘要

癌症干细胞(CSCs)是肿瘤细胞中最具恶性的亚群,具有致瘤潜力和对化疗的抗性。这些特性使癌症干细胞成为开发靶向抗肿瘤治疗的一个有前景的靶点,这在高度侵袭性癌症中尤其迫切需要。然而,正确识别具有干细胞特性的癌细胞仍然是一个挑战。一种新开发的基于慢病毒的报告基因SORE6能够通过测量胚胎干细胞因子SOX2和OCT4的基因表达来直接识别癌症干细胞。在当前研究中,对该报告基因进行了修饰,以便通过免疫磁珠分离法分离SOX2^(+)/OCT4^(+)细胞,然后用于转导HCC1806和MDA-MB-453三阴性乳腺癌(TNBC)细胞系。为了验证修饰后的报告基因,分离出SOX2^(+)/OCT4^(+)细胞群,并分析其中多能性关键转录因子NANOG的含量,其表达受SOX2/OCT4调控。评估了每个细胞系中SOX2^(+)/OCT4^(+)细胞的百分比。在分离出的SOX2^(+)/OCT4^(+)细胞组分中发现NANOG蛋白含量增加,表明修饰后的报告基因适用于进一步研究癌症干细胞亚群。

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