Liquid biopsy for patients with IBD-associated neoplasia
Abstract Background It is often difficult to diagnose inflammatory bowel disease (IBD)-associated neoplasia endoscopically due to background inflammation. In addition, due to the absence of sensitive tumor biomarkers, countermeasures against IBD-associated neoplasia are crucial. The purpose of this...
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BMC
2020-12-01
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Series: | BMC Cancer |
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Online Access: | https://doi.org/10.1186/s12885-020-07699-z |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hideaki Kinugasa Sakiko Hiraoka Kazuhiro Nouso Shumpei Yamamoto Mami Hirai Hiroyuki Terasawa Eriko Yasutomi Shohei Oka Masayasu Ohmori Yasushi Yamasaki Toshihiro Inokuchi Masahiro Takahara Keita Harada Takehiro Tanaka Hiroyuki Okada |
spellingShingle |
Hideaki Kinugasa Sakiko Hiraoka Kazuhiro Nouso Shumpei Yamamoto Mami Hirai Hiroyuki Terasawa Eriko Yasutomi Shohei Oka Masayasu Ohmori Yasushi Yamasaki Toshihiro Inokuchi Masahiro Takahara Keita Harada Takehiro Tanaka Hiroyuki Okada Liquid biopsy for patients with IBD-associated neoplasia BMC Cancer IBD-associated neoplasia IBD-associated cancer Liquid biopsy ctDNA |
author_facet |
Hideaki Kinugasa Sakiko Hiraoka Kazuhiro Nouso Shumpei Yamamoto Mami Hirai Hiroyuki Terasawa Eriko Yasutomi Shohei Oka Masayasu Ohmori Yasushi Yamasaki Toshihiro Inokuchi Masahiro Takahara Keita Harada Takehiro Tanaka Hiroyuki Okada |
author_sort |
Hideaki Kinugasa |
title |
Liquid biopsy for patients with IBD-associated neoplasia |
title_short |
Liquid biopsy for patients with IBD-associated neoplasia |
title_full |
Liquid biopsy for patients with IBD-associated neoplasia |
title_fullStr |
Liquid biopsy for patients with IBD-associated neoplasia |
title_full_unstemmed |
Liquid biopsy for patients with IBD-associated neoplasia |
title_sort |
liquid biopsy for patients with ibd-associated neoplasia |
publisher |
BMC |
series |
BMC Cancer |
issn |
1471-2407 |
publishDate |
2020-12-01 |
description |
Abstract Background It is often difficult to diagnose inflammatory bowel disease (IBD)-associated neoplasia endoscopically due to background inflammation. In addition, due to the absence of sensitive tumor biomarkers, countermeasures against IBD-associated neoplasia are crucial. The purpose of this study is to develop a new diagnostic method through the application of liquid biopsy. Methods Ten patients with IBD-associated cancers and high-grade dysplasia (HGD) with preserved tumor tissue and blood were included. Tumor and non-tumor tissues were analyzed for 48 cancer-related genes using next-generation sequencing. Simultaneously, circulating tumor DNA (ctDNA) was analyzed for mutations in the target genes using digital PCR. Results Out of 10 patients, seven had IBD-related cancer and three had IBD-related HGD. Two patients had carcinoma in situ; moreover, three had stageII and two had stage III. To avoid false positives, the mutation rate cutoff was set at 5% based on the control results; seven of 10 (70%) tumor tissue samples were mutation-positive. Mutation frequencies for each gene were as follows: TP53 (20.9%; R136H), TP53 (25.0%; C110W), TP53 (8.5%; H140Q), TP53 (31.1%; R150W), TP53 (12.8%; R141H), KRAS (40.0%; G12V), and PIK3CA (34.1%; R 88Q). The same mutations were detected in the blood of these seven patients. However, no mutations were detected in the blood of the remaining three patients with no tumor tissue mutations. The concordance rate between tumor tissue DNA and blood ctDNA was 100%. Conclusion Blood liquid biopsy has the potential to be a new method for non-invasive diagnosis of IBD-associated neoplasia. |
topic |
IBD-associated neoplasia IBD-associated cancer Liquid biopsy ctDNA |
url |
https://doi.org/10.1186/s12885-020-07699-z |
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doaj-54088b9638b343bf84f9024e0c89c9e02020-12-06T12:54:18ZengBMCBMC Cancer1471-24072020-12-012011610.1186/s12885-020-07699-zLiquid biopsy for patients with IBD-associated neoplasiaHideaki Kinugasa0Sakiko Hiraoka1Kazuhiro Nouso2Shumpei Yamamoto3Mami Hirai4Hiroyuki Terasawa5Eriko Yasutomi6Shohei Oka7Masayasu Ohmori8Yasushi Yamasaki9Toshihiro Inokuchi10Masahiro Takahara11Keita Harada12Takehiro Tanaka13Hiroyuki Okada14Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Pathology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesDepartment of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical SciencesAbstract Background It is often difficult to diagnose inflammatory bowel disease (IBD)-associated neoplasia endoscopically due to background inflammation. In addition, due to the absence of sensitive tumor biomarkers, countermeasures against IBD-associated neoplasia are crucial. The purpose of this study is to develop a new diagnostic method through the application of liquid biopsy. Methods Ten patients with IBD-associated cancers and high-grade dysplasia (HGD) with preserved tumor tissue and blood were included. Tumor and non-tumor tissues were analyzed for 48 cancer-related genes using next-generation sequencing. Simultaneously, circulating tumor DNA (ctDNA) was analyzed for mutations in the target genes using digital PCR. Results Out of 10 patients, seven had IBD-related cancer and three had IBD-related HGD. Two patients had carcinoma in situ; moreover, three had stageII and two had stage III. To avoid false positives, the mutation rate cutoff was set at 5% based on the control results; seven of 10 (70%) tumor tissue samples were mutation-positive. Mutation frequencies for each gene were as follows: TP53 (20.9%; R136H), TP53 (25.0%; C110W), TP53 (8.5%; H140Q), TP53 (31.1%; R150W), TP53 (12.8%; R141H), KRAS (40.0%; G12V), and PIK3CA (34.1%; R 88Q). The same mutations were detected in the blood of these seven patients. However, no mutations were detected in the blood of the remaining three patients with no tumor tissue mutations. The concordance rate between tumor tissue DNA and blood ctDNA was 100%. Conclusion Blood liquid biopsy has the potential to be a new method for non-invasive diagnosis of IBD-associated neoplasia.https://doi.org/10.1186/s12885-020-07699-zIBD-associated neoplasiaIBD-associated cancerLiquid biopsyctDNA |