长非编码 RNA 作为卵巢癌 (OC) 潜在的生物标记物和化疗耐药性调节剂的关键作用。

IF 3.8 2区 生物学 Q2 GENETICS & HEREDITY
Human Genetics Pub Date : 2024-02-01 Epub Date: 2024-01-26 DOI:10.1007/s00439-023-02635-0
Shika Hanif Malgundkar, Yahya Tamimi
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引用次数: 0

摘要

卵巢癌(OC)是一种致命的妇科疾病,由于无症状和缺乏有效的早期生物标志物,通常在晚期才被诊断出来。以往的研究发现,在卵巢癌中表达异常的基因无法用甲基化或突变来解释,这表明存在其他的基因调控机制。人类转录组研究的最新进展促使人们开始研究作为癌症基因表达调控因子的非编码 RNA(ncRNA)。长非编码 RNA(lncRNA)是一类长度超过 200 个核苷酸的 ncRNA,已被确定为生理过程和人类疾病(包括癌症)的关键调控因子。研究还发现,lncRNA表达失调在卵巢癌发生中起着至关重要的作用,这表明它们有可能成为改善卵巢癌管理的新型非侵入性生物标志物。然而,尽管已经发现了数千个 lncRNA,但只有一个被批准作为癌症生物标志物用于临床,这凸显了在这一领域开展进一步研究的重要性。除了作为生物标记物的潜力外,lncRNA 还与化疗耐药性的调节有关,而化疗耐药性是 OC 的一个主要问题。一些研究发现了药物治疗时 lncRNA 表达的改变,进一步强调了它们调节化疗耐药性的潜力。在这篇综述中,我们将重点介绍 lncRNA 的特点、功能及其作为 OC 肿瘤标志物的潜力。我们还讨论了一些数据库,这些数据库提供了各种癌症类型中lncRNAs的详细信息。尽管lncRNAs的潜力巨大,但仍有必要开展进一步的研究,以充分了解它们在癌症中的作用,并制定有效的策略来对抗这种毁灭性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The pivotal role of long non-coding RNAs as potential biomarkers and modulators of chemoresistance in ovarian cancer (OC).

The pivotal role of long non-coding RNAs as potential biomarkers and modulators of chemoresistance in ovarian cancer (OC).

Ovarian cancer (OC) is a fatal gynecological disease that is often diagnosed at later stages due to its asymptomatic nature and the absence of efficient early-stage biomarkers. Previous studies have identified genes with abnormal expression in OC that couldn't be explained by methylation or mutation, indicating alternative mechanisms of gene regulation. Recent advances in human transcriptome studies have led to research on non-coding RNAs (ncRNAs) as regulators of cancer gene expression. Long non-coding RNAs (lncRNAs), a class of ncRNAs with a length greater than 200 nucleotides, have been identified as crucial regulators of physiological processes and human diseases, including cancer. Dysregulated lncRNA expression has also been found to play a crucial role in ovarian carcinogenesis, indicating their potential as novel and non-invasive biomarkers for improving OC management. However, despite the discovery of several thousand lncRNAs, only one has been approved for clinical use as a biomarker in cancer, highlighting the importance of further research in this field. In addition to their potential as biomarkers, lncRNAs have been implicated in modulating chemoresistance, a major problem in OC. Several studies have identified altered lncRNA expression upon drug treatment, further emphasizing their potential to modulate chemoresistance. In this review, we highlight the characteristics of lncRNAs, their function, and their potential to serve as tumor markers in OC. We also discuss a few databases providing detailed information on lncRNAs in various cancer types. Despite the promising potential of lncRNAs, further research is necessary to fully understand their role in cancer and develop effective strategies to combat this devastating disease.

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来源期刊
Human Genetics
Human Genetics 生物-遗传学
CiteScore
10.80
自引率
3.80%
发文量
94
审稿时长
1 months
期刊介绍: Human Genetics is a monthly journal publishing original and timely articles on all aspects of human genetics. The Journal particularly welcomes articles in the areas of Behavioral genetics, Bioinformatics, Cancer genetics and genomics, Cytogenetics, Developmental genetics, Disease association studies, Dysmorphology, ELSI (ethical, legal and social issues), Evolutionary genetics, Gene expression, Gene structure and organization, Genetics of complex diseases and epistatic interactions, Genetic epidemiology, Genome biology, Genome structure and organization, Genotype-phenotype relationships, Human Genomics, Immunogenetics and genomics, Linkage analysis and genetic mapping, Methods in Statistical Genetics, Molecular diagnostics, Mutation detection and analysis, Neurogenetics, Physical mapping and Population Genetics. Articles reporting animal models relevant to human biology or disease are also welcome. Preference will be given to those articles which address clinically relevant questions or which provide new insights into human biology. Unless reporting entirely novel and unusual aspects of a topic, clinical case reports, cytogenetic case reports, papers on descriptive population genetics, articles dealing with the frequency of polymorphisms or additional mutations within genes in which numerous lesions have already been described, and papers that report meta-analyses of previously published datasets will normally not be accepted. The Journal typically will not consider for publication manuscripts that report merely the isolation, map position, structure, and tissue expression profile of a gene of unknown function unless the gene is of particular interest or is a candidate gene involved in a human trait or disorder.
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