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间充质干细胞条件培养基对大肠癌细胞系的凋亡作用。

Apoptotic effects of mesenchymal stem cells' conditioned medium on colorectal cancer cell lines.

作者信息

Khamooshi Roya, Salimi Ali, Halabian Raheleh, Saeedi Pardis

机构信息

Department of Molecular and Cellular Sciences, Faculty of Advanced Sciences and Technology, Pharmaceutical Sciences Branch, Islamic Azad University Tehran, Iran.

Tissue Engineering and Regenerative Medicine Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.

出版信息

Tissue Cell. 2023 Dec;85:102247. doi: 10.1016/j.tice.2023.102247. Epub 2023 Oct 15.

Abstract

Multipotent Mesenchymal stem cells (MSCs) have vigorous immunomodulatory activity, apoptotic effects, and the capacity to migrate to inflammatory and tumor sites. This study focuses on the apoptotic effects of MSCs conditioned medium (CM) on colorectal cancer cell lines. MSCs were preconditioned with lipopolysaccharide (LPS) to induce apoptosis in colorectal cancer cells. The conditioned medium (LPS-CM) from the preconditioned cells was isolated and used to treat colorectal cancer cells (HT29 and SW48). The survival and proliferation of cancer cells were assessed using Trypan blue staining and MTT assay. The apoptosis rate was evaluated through flow cytometry analysis and caspase-3 activity. Additionally, Real-Time PCR was used to measure the mRNA level of apoptotic and anti-apoptotic factors, including bcl2, bax, and p53 genes. The results showed that LPS-CM significantly increased (p < 0.001) the percentage of apoptosis in the SW48 and HT29 cell lines. Caspase-3 activity significantly increased (p < 0.001) in these cell lines after treatment with LPS-CM. The mRNA level of bcl2 was significantly decreased (p < 0.001), while bax and p53 genes were significantly overexpressed (p < 0.001) in the LPS-CM treated cell lines. Notably, the mRNA level of bcl2 and bax genes was significantly altered at a higher concentration of LPS-CM. In conclusion, the conditioned medium from LPS-preconditioned MSCs can effectively induce apoptosis in colorectal cancer cells. This finding suggests that LPS-CM could be a potential strategy for inhibiting the proliferation and progression of colorectal cancer cells.

摘要

多能间充质干细胞(MSCs)具有强大的免疫调节活性、凋亡作用以及迁移至炎症和肿瘤部位的能力。本研究聚焦于MSCs条件培养基(CM)对结肠癌细胞系的凋亡作用。用脂多糖(LPS)预处理MSCs以诱导结肠癌细胞凋亡。分离预处理细胞的条件培养基(LPS-CM)并用于处理结肠癌细胞(HT29和SW48)。使用台盼蓝染色和MTT法评估癌细胞的存活和增殖。通过流式细胞术分析和caspase-3活性评估凋亡率。此外,使用实时荧光定量PCR测量凋亡和抗凋亡因子的mRNA水平,包括bcl2、bax和p53基因。结果显示,LPS-CM显著增加(p<0.001)SW48和HT29细胞系中的凋亡百分比。用LPS-CM处理后,这些细胞系中的caspase-3活性显著增加(p<0.001)。在LPS-CM处理的细胞系中,bcl2的mRNA水平显著降低(p<0.001),而bax和p53基因显著过表达(p<0.001)。值得注意的是,在较高浓度的LPS-CM下,bcl2和bax基因的mRNA水平发生了显著变化。总之,LPS预处理的MSCs的条件培养基可有效诱导结肠癌细胞凋亡。这一发现表明,LPS-CM可能是抑制结肠癌细胞增殖和进展的潜在策略。

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