Comparison of Somatic Mutation Profiles Between Formalin-Fixed Paraffin Embedded Tissues and Plasma Cell-Free DNA from Ovarian Cancer Patients Before and After Surgery.

Q2 Biochemistry, Genetics and Molecular Biology
BioResearch Open Access Pub Date : 2020-03-13 eCollection Date: 2020-01-01 DOI:10.1089/biores.2019.0031
Marianna Jagelkova, Katarina Zelinova, Zuzana Laucekova, Martina Bobrovska, Zuzana Dankova, Marian Grendar, Karol Dokus
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Abstract

Ovarian carcinogenesis can be induced by a large number of somatic gene mutations. Circulating tumor DNA (ctDNA) released into peripheral blood can provide insights into the genomic landscape of cancer cells and monitor their dynamics. Our aim was to detect and compare the genetic profiles in tumor tissue and plasma before and after tumor resection in ovarian cancer patients. All three samples were collected from each patient. In this study, we used a commercial cancer panel to identify somatic mutations in 26 genes in seven selected patients through next-generation sequencing on the Illumina platform. Overall, 16 variants with pathogenic effect were identified in the TP53, PIK3CA, PTEN, APC, NRAS, KRAS, GNAS, and MET genes involved in important signaling pathways. The genetic alterations found in the presurgical plasma in six of seven ovarian cancer patients were no longer present in the plasma after tumor surgical removal. Identical variants in formalin-fixed paraffin embedded (FFPE) tissues and preoperative plasma specimens were observed in only two cases. These findings suggest that the detected presurgical pathogenic variants absent in postsurgery plasma are associated with the primary ovarian tumor. Finally, the low-identified concordance between FFPE and plasma can be due to various factors, but most likely to high tumor heterogeneity and low ctDNA level.

Abstract Image

卵巢癌患者手术前后福尔马林固定石蜡包埋组织与血浆无细胞 DNA 的体细胞突变谱比较
大量体细胞基因突变可诱发卵巢癌。释放到外周血中的循环肿瘤 DNA(ctDNA)可以让人了解癌细胞的基因组情况并监测其动态变化。我们的目的是检测和比较卵巢癌患者肿瘤切除前后肿瘤组织和血浆中的基因图谱。我们从每位患者身上采集了三种样本。在这项研究中,我们使用了一个商业癌症面板,通过在 Illumina 平台上进行下一代测序,在七名选定的患者中确定了 26 个基因的体细胞突变。总体而言,在涉及重要信号通路的 TP53、PIK3CA、PTEN、APC、NRAS、KRAS、GNAS 和 MET 基因中发现了 16 个具有致病作用的变异。在七名卵巢癌患者中,有六名患者手术前血浆中发现的基因变异在肿瘤手术切除后血浆中已不复存在。只有两个病例在福尔马林固定石蜡包埋(FFPE)组织和术前血浆标本中观察到了相同的变异。这些发现表明,手术前检测到的致病变体在手术后血浆中不存在,这与原发性卵巢肿瘤有关。最后,FFPE 和血浆之间的低识别一致性可能是由多种因素造成的,但最有可能的原因是肿瘤异质性高和 ctDNA 水平低。
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来源期刊
BioResearch Open Access
BioResearch Open Access Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
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1
期刊介绍: BioResearch Open Access is a high-quality open access journal providing peer-reviewed research on a broad range of scientific topics, including molecular and cellular biology, tissue engineering, regenerative medicine, stem cells, gene therapy, systems biology, genetics, virology, and neuroscience. The Journal publishes basic science and translational research in the form of original research articles, comprehensive review articles, mini-reviews, rapid communications, brief reports, technology reports, hypothesis articles, perspectives, and letters to the editor.
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