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重编程的癌细胞能否作为(诱导性)癌症干细胞的替代来源?

Can the reprogrammed cancer cells serve as an alternative source of (induced) cancer stem cells?

作者信息

Stelcer Ewelina, Blatkiewicz Małgorzata, Jopek Karol, Suchorska Wiktoria Maria, Rucinski Marcin

机构信息

Department of Histology and Embryology, Poznan University of Medical Sciences, Poznan, Poland.

Department of Electroradiology, Poznan University of Medical Sciences, Poznan, Poland.

出版信息

Rep Pract Oncol Radiother. 2024 Dec 4;29(5):651-656. doi: 10.5603/rpor.102821. eCollection 2024.

Abstract

BACKGROUND

Cancer stem cells (CSCs) constitute a small and elusive subpopulation of cancer cells within a tumor mass and are characterized by stem cell properties. Reprogrammed CSCs exhibit similar capability to initiate tumor growth, metastasis, and chemo- and radio-resistance and have similar gene profiles to primary CSCs. However, the efficiency of cancer cell reprogramming remained relatively low. There is limited literature available on the reprogramming of lung cancer cells. Hence, in this study we have conducted reprogramming of human lung cancer cells towards more benign type of cells.

MATERIALS AND METHODS

The reprogramming process was carried out with the use of STEMCCA vector. We have investigated the gene expression profile of induced CSCs (iCSCs) using the microarray technique.

RESULTS

The lung iCSCs demonstrate morphology characteristics of induced pluripotent stem cells (iPSCs) and gene expression profile that significantly differ from cells before reprogramming. We have also presented the elevated level of expression of genes associated with the cancer stemness and thus revealed new interesting CSC-like molecular markers.

CONCLUSIONS

These preliminary results demonstrated that the reprogramming process leads to the remarkable changes in cells at the gene level and has potential to be an alternative method of generating CSC-like cells.

摘要

背景

癌症干细胞(CSCs)是肿瘤块内一小部分难以捉摸的癌细胞亚群,具有干细胞特性。重编程的癌症干细胞表现出相似的启动肿瘤生长、转移以及化疗和放疗抗性的能力,并且与原发性癌症干细胞具有相似的基因谱。然而,癌细胞重编程的效率仍然相对较低。关于肺癌细胞重编程的文献有限。因此,在本研究中,我们对人肺癌细胞进行了重编程,使其向更良性的细胞类型转变。

材料与方法

使用STEMCCA载体进行重编程过程。我们利用微阵列技术研究了诱导性癌症干细胞(iCSCs)的基因表达谱。

结果

肺iCSCs表现出诱导多能干细胞(iPSCs)的形态特征以及与重编程前细胞显著不同的基因表达谱。我们还展示了与癌症干性相关基因的表达水平升高,从而揭示了新的有趣的类癌症干细胞分子标志物。

结论

这些初步结果表明,重编程过程导致细胞在基因水平上发生显著变化,并且有可能成为生成类癌症干细胞的替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17d7/11698551/c672acebbea0/rpor-29-5-651f1.jpg

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