MCM10 expression is linked to cervical cancer aggressiveness.

Frontiers in molecular medicine Pub Date : 2023-02-22 eCollection Date: 2023-01-01 DOI:10.3389/fmmed.2023.1009903
Sumayyah M Q Ahmed, Suparna Laha, Ranajit Das, Mariam Anjum Ifthikar, Shankar Prasad Das
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Abstract

Cervical cancer screening is a challenge mainly in developing countries. In developed countries, both incidence and mortality rates have been decreasing due to well organized screening programs. One of the potential biomarkers being exploited are the minichromosome maintenance proteins (MCMs), which show both specificity and sensitivity. MCM2-7 are involved in DNA replication initiation and elongation, and the MCM subunits are highly expressed in malignant tissues. Unlike other MCMs, MCM10, which is not part of the core helicase complex, is a critical determinant of origin activation and its levels are limiting in cancer cells. In this study, we performed bioinformatic analysis on the expression profile of all DNA replication associated MCM proteins in cervical cancer. MCM10 showed a relatively higher expression profile compared to the other MCMs. The mRNA expression levels of the MCMs were significantly increased in tumour tissues compared to normal, and MCM10 showed a fold change of 3.4. In order to understand if MCM10 is associated with the aggressiveness of cervical cancer, we looked into the mRNA expression pattern of MCM10 in three cervical cancer cell lines and one normal cervical cell line. MCM10 expression was significantly higher in the case of the more aggressive cancer cell line HeLa compared to controls. MCM10, therefore, can serve as a prominent biomarker for cancer progression and thus aid in early detection to control the spread of cancer cells. Our results show that MCM10 expression levels in cervical cancer cell lines are associated with cancer aggressiveness, demonstrating its clinical significance.

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MCM10表达与宫颈癌症侵袭性相关
子宫颈癌症筛查主要在发展中国家是一项挑战。在发达国家,由于组织良好的筛查计划,发病率和死亡率都在下降。正在开发的潜在生物标志物之一是微染色体维持蛋白(MCMs),它显示出特异性和敏感性。MCM2-7参与DNA复制的起始和延伸,并且MCM亚基在恶性组织中高度表达。与其他MCM不同,MCM10不是核心解旋酶复合物的一部分,是起源激活的关键决定因素,其水平在癌症细胞中受到限制。在本研究中,我们对癌症中所有DNA复制相关的MCM蛋白的表达谱进行了生物信息学分析。与其它MCM相比,MCM10显示出相对较高的表达谱。与正常人相比,肿瘤组织中MCMs的mRNA表达水平显著增加,MCM10显示3.4倍的变化。为了了解MCM10是否与癌症的侵袭性有关,我们研究了三种癌症宫颈细胞系和一种正常宫颈细胞系中MCM10的mRNA表达模式。与对照相比,在更具侵袭性的癌症细胞系HeLa的情况下,MCM10的表达显著更高。因此,MCM10可以作为癌症进展的显著生物标志物,从而有助于早期检测以控制癌症细胞的扩散。我们的研究结果表明,MCM10在宫颈癌症细胞系中的表达水平与癌症侵袭性有关,表明其临床意义。
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