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人类假性黏液瘤腹膜和阑尾黏液性肿瘤的遗传特征和分子亚型:系统评价。

The genetic profile and molecular subtypes of human pseudomyxoma peritonei and appendiceal mucinous neoplasms: a systematic review.

机构信息

School of Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton, SO17 1BJ, UK.

Pathology Department, Faculty of Medicine, Alexandria University, Alexandria, Egypt.

出版信息

Cancer Metastasis Rev. 2023 Mar;42(1):335-359. doi: 10.1007/s10555-023-10088-0. Epub 2023 Feb 1.

Abstract

Pseudomyxoma peritonei (PMP) is a rare, progressive, slowly growing neoplastic condition which is poorly understood, with a 5-year progression-free survival rate as low as 48%. PMP is most commonly caused by appendiceal mucinous neoplasms (AMN), and understanding their genetic biology and pathogenicity may allow for the development of better novel systemic treatments to target key deleterious mutations and the implicated pathways. The primary aim of this systematic review was to identify the genetic profile of histologically confirmed human PMP or AMN samples. The secondary aim was to identify whether genetic marks could be used to predict patient survival. Ovid EMBASE, Ovid MEDLINE, PubMed, and Web of Science were searched to identify studies investigating the genetic profile of histologically-confirmed human PMP or AMN samples. We review findings of 46 studies totalling 2181 tumour samples. The most frequently identified somatic gene mutations in patients with PMP included KRAS (38-100%), GNAS (17-100%), and TP53 (5-23%); however, there were conflicting results of their effect on survival. Three studies identified molecular subtypes based on gene expression profiles classifying patients into oncogene-enriched, immune-enriched, and mixed molecular subtypes with prognostic value. This review summarises the current literature surrounding genetic aberrations in PMP and AMNs and their potential utility for targeted therapy. Given the recent advances in clinical trials to directly target KRAS and GNAS mutations in other cancers, we propose a rationale to explore these mutations in future pre-clinical studies in PMP with a view for a future clinical trial.

摘要

腹膜假性黏液瘤(PMP)是一种罕见的、进行性的、生长缓慢的肿瘤性疾病,目前人们对其了解甚少,5 年无进展生存率低至 48%。PMP 最常见于阑尾黏液性肿瘤(AMN),了解其遗传生物学和发病机制可能有助于开发更好的新型全身治疗方法,以靶向关键有害突变和相关途径。本系统评价的主要目的是确定组织学证实的人类 PMP 或 AMN 样本的遗传特征。次要目的是确定遗传标记是否可用于预测患者的生存情况。我们在 Ovid EMBASE、Ovid MEDLINE、PubMed 和 Web of Science 上进行了检索,以确定研究组织学证实的人类 PMP 或 AMN 样本遗传特征的研究。我们综述了 46 项研究的结果,这些研究共涉及 2181 个肿瘤样本。在 PMP 患者中最常发现的体细胞基因突变包括 KRAS(38-100%)、GNAS(17-100%)和 TP53(5-23%);然而,它们对生存的影响存在矛盾的结果。有 3 项研究根据基因表达谱确定了分子亚型,将患者分为致癌基因富集型、免疫富集型和混合分子亚型,具有预后价值。本综述总结了目前关于 PMP 和 AMN 中遗传异常及其在靶向治疗中的潜在应用的文献。鉴于最近在其他癌症中直接靶向 KRAS 和 GNAS 突变的临床试验取得了进展,我们建议在未来的 PMP 临床前研究中探索这些突变,以期进行未来的临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edd8/10014681/3f8252d41dc6/10555_2023_10088_Fig1_HTML.jpg

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