I型和II型子宫内膜癌的干细胞群有差异吗?试点研究。

Journal of mother and child Pub Date : 2025-05-24 eCollection Date: 2025-02-01 DOI:10.34763/jmotherandchild.20252901.d-24-00041
N Muthuraman, Anitha Thomas, Thomas Samuel Ram, K M Mohankumar, Premila Abraham
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引用次数: 0

摘要

背景:子宫内膜癌的发病率在全球范围内呈上升趋势。癌症干细胞现在被认为是肿瘤复发和转移的驱动力。我们研究了I型和II型子宫内膜癌中癌症干细胞群体比例和干性基因表达是否存在差异。材料和方法:取子宫切除术患者的I型和II型子宫内膜肿瘤组织。用胶原酶消化肿瘤组织,建立原代培养。在这两种癌症的原代培养中,我们使用流式细胞术测量了在其表面表达cd133和CXCR4的癌症干细胞群体的比例。我们还在这两种癌症类型中寻找与干性、干性调节因子和转移标志物相关的基因表达。结果:我们发现II型子宫内膜癌中表达CD133和CXCR4的癌症干细胞群体比例高于I型子宫内膜癌。此外,与干性和异常转录组相关的基因(Nanog, ALDH, EZH2)在II型子宫内膜癌中被发现上调。结论:我们的研究表明,干细胞在2型子宫内膜癌中的比例高于1型子宫内膜癌。本研究的发现将引导我们进行更大样本量的研究,看看II型子宫内膜癌中干细胞群的增加是否可能是其预后不良的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Is There Any Difference in Stem Cell Population between Type I and Type II Endometrial Cancer? A Pilot Study.

Background: The incidence of endometrial cancer is increasing globally. Cancer stem cells are now considered the driving force for tumour recurrence and metastasis. We studied whether the proportion of cancer stem cell population and stemness gene expression differ in type I and type II endometrial cancer.

Materials and methods: Type I and type II endometrial tumour tissues were obtained from patients who underwent hysterectomy. The tumour tissue was digested using collagenase, and we established a primary culture. In the primary cultures established from these two types of cancer, we used flow cytometry to measure the proportion of the cancer stem cell population expressing CD 133 and CXCR4 on its surface. We also looked for the expression of genes related to stemness, regulators of stemness, and markers of metastasis in both these cancer types.

Results: We found that the proportion of cancer stem cell population that expresses CD133 and CXCR4 was higher in type II endometrial cancer than in type I endometrial cancer. Also, genes (Nanog, ALDH, EZH2) related to stemness and aberrant transcriptome were found to be upregulated in type II endometrial cancer.

Conclusion: Our study demonstrates that the proportion of stem cells in type 2 endometrial cancer is higher than in type I endometrial cancer. The findings of this study should lead us to investigate with a larger sample size and see if the increase in the stem cell population in type II endometrial cancer may be the reason for its poor prognosis.

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