Suppr超能文献

早期宫颈癌根治性手术后致癌性体细胞突变的临床意义。

Clinical implication of oncogenic somatic mutations in early-stage cervical cancer with radical hysterectomy.

机构信息

Department of Obstetrics and Gynecology, Fukushima Medical University School of Medicine, Fukushima, 960-1295, Japan.

Medical-Industrial Translational Research Center, Fukushima Medical University School of Medicine, Fukushima, 960-1295, Japan.

出版信息

Sci Rep. 2020 Oct 30;10(1):18734. doi: 10.1038/s41598-020-72518-1.

Abstract

It is well known that tumour initiation and progression are primarily an accumulation of genetic mutations. The mutation status of a tumour may predict prognosis and enable better selection of targeted therapies. In the current study, we analysed a total of 55 surgical tumours from stage IB-IIB cervical cancer (CC) patients who had undergone radical hysterectomy including pelvic lymphadenectomy, using a cancer panel covering 50 highly mutated tumorigenesis-related genes. In 35 patients (63.6%), a total 52 mutations were detected (58.3% in squamous cell carcinoma, 73.7% in adenocarcinoma), mostly in PIK3CA (34.5%) and KRAS and TP53 (9.1%). Being mutation-positive was significantly correlated with pelvic lymph node (PLN) metastasis (P = 0.035) and tended to have a worse overall survival (P = 0.076). In particular, in the patients with squamous cell carcinoma, there was a significant association between being mutation-positive and relapse-free survival (P = 0.041). The patients with PLN metastasis had a significantly worse overall survival than those without (P = 0.006). These results indicate that somatic mutation status is a predictive biomarker for PLN metastasis in early-stage CC, and is consequently related to poor prognosis. Therefore, comprehensive genetic mutations, rather than a single genetic mutation, should be examined widely in order to identify novel genetic indicators with clinical usefulness.

摘要

众所周知,肿瘤的发生和发展主要是遗传突变的积累。肿瘤的突变状态可以预测预后,并能更好地选择靶向治疗。在本研究中,我们分析了 55 例接受根治性子宫切除术(包括盆腔淋巴结切除术)的 IB-IIB 期宫颈癌(CC)患者的 55 例手术肿瘤,使用了一个涵盖 50 个高度突变的肿瘤发生相关基因的癌症panel。在 35 名患者(63.6%)中,总共检测到 52 个突变(鳞癌 58.3%,腺癌 73.7%),主要发生在 PIK3CA(34.5%)和 KRAS 和 TP53(9.1%)。突变阳性与盆腔淋巴结(PLN)转移显著相关(P=0.035),总生存期也倾向于更差(P=0.076)。特别是在鳞癌患者中,突变阳性与无复发生存率之间存在显著相关性(P=0.041)。有 PLN 转移的患者总生存期明显比没有转移的患者差(P=0.006)。这些结果表明,体细胞突变状态是早期 CC 中 PLN 转移的预测生物标志物,因此与预后不良相关。因此,为了识别具有临床用途的新的遗传指标,应该广泛检查综合的遗传突变,而不是单一的遗传突变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff4f/7599240/7dc514960085/41598_2020_72518_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验