Skip to main content
  • Research article
  • Open access
  • Published:

Liquid biopsy for patients with IBD-associated neoplasia



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.


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.


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%.


Blood liquid biopsy has the potential to be a new method for non-invasive diagnosis of IBD-associated neoplasia.

Peer Review reports


It is widely accepted that cancers occur in patients suffering from IBD and these cancers are distinguished from sporadic colorectal cancers as IBD-associated cancers. Eaden et al. [1] reported the incidence rates of IBD-associated cancers as 2.1%/10 years, 8.5%/20 years, and 17.8%/30 years, while Rutter et al. [2] reported the incidence rates as 2.5%/20 years, 7.6%/30 years, and 10.8%/40 years. Although there is a slight variation in the rates of IBD-associated cancers from several reports [3], it is still a challenge to prevent IBD-associated cancers in patients suffering from IBD.

The functionality of colonoscopy as a surveillance method for the detection of IBD-associated cancers has been studied. Although its contribution to colorectal cancer detection has long been known, a systemic review revealed that colonoscopy for IBD diagnosis not only improves the detection rate of colorectal cancer but also its effectiveness in colorectal cancer-associated deaths [4]. However, endoscopic diagnosis of cancer in IBD is often difficult due to background inflammation, and countermeasures are imperative.

Randomized biopsy has been used as a surveillance method for IBD-associated cancers mainly in Europe and the United States, but the usefulness of targeted biopsy has also been reported with the development of endoscopic instruments [5]. In addition, the application of indigo staining and NBI (narrow band imaging) has been demonstrated in various studies and the surveillance methods have been reviewed [6, 7]. However, none of these methods provides a breakthrough for the existing methods and clinicians are still in search for the other alternatives and improvisations.

On the other hand, new findings about the genes involved in IBD-associated cancers have been reported in the last few years. Compared to the mutations involved in sporadic colorectal cancer, the involvement of APC mutations is lower and new findings such as the involvement of TP53, KRAS, SMAD4, and IDH1 have been revealed [8,9,10,11,12].

Liquid biopsy has been attracting attention as a non-invasive method for cancer treatment [13]. Traditionally, a direct biopsy of the tumor is considered to be the only way to diagnose cancer, but this new method of liquid biopsy is drawing attention because it can obtain tumor information from blood, which is comparable to that of the conventional methods [14]. Endoscopic diagnosis of cancer in IBD is often difficult due to the background inflammation and the lack of sensitive tumor biomarkers. The application of liquid biopsy appears to be the best for the detection of IBD-associated cancers.

The purpose of the current study was to examine and detect the presence of mutated genes in blood via circulating tumor DNA (ctDNA) of IBD-associated tumors and to examine the functionality of liquid biopsy by comparing tumor tissue DNA with ctDNA.


Patients and genes

Ten patients with IBD-associated cancers and high-grade dysplasia, treated at the Okayama University Hospital from 2004 to 2015, with preserved tumor tissue and blood were included in this study. Tumor tissues were analyzed using next-generation sequencers, while blood was simultaneously analyzed for mutations using digital PCR. We selected 48 cancer-related genes based on previously published information of whole genome analysis [10, 11]. These genes included the following: ABL1, AKT1, ALK, AR, ATM, BRAF, CDKN2A, CSF1R, CTNNB1, EGFR, ERBB2, ERBB4, FANCA, FANCC, FANCF, FANCG, FGFR1, FGFR2, FGFR3, FLT3, HRAS, IDH1, IDH2, JAK2, JAK3, KIT, KRAS, MAP 2 K1, MAP 2 K2, MAP 2 K4, MET, NOTCH1, NPM1, NRAS, PDGFRA, PIK3CA, PIK3R1, PTEN, RET, RUNX1, SMAD4, SMO, SRC, STK11, TP53, VHL, WT1, and hTERT. All patients provided written informed consent prior to enrolment. This study was approved by the ethics committee of Okayama University Hospital (1602–047/1506–070) and conducted in accordance with the Declaration of Helsinki.

Also, not only non-cancerous tissue samples paired to cancerous tissue samples but also ten patients with IBD (5 Crohn and 5 UC) without a tumor have been observed as control in this study.

Extraction of DNA

Formalin fixed paraffin embedded (FFPE) samples were obtained by surgical resection. Histological examinations confirmed that these samples contained a minimum of 30% tumor cells. We extracted DNA from 5-μm thick sections from FFPE samples using a QIAamp DNA FFPE Tissue Kit (Qiagen, Valencia, CA, USA), according to the manufacturer’s instructions.

All blood samples were collected prior to initial treatment. DNA was extracted from each source according to the manufacturer’s instructions. Plasma samples were separated by centrifugation (3000 rpm, 10 min, 4 °C) within 3 h of blood collection. The samples were then stored at − 30 °C for subsequent DNA extraction. Cell free DNA (cfDNA) was extracted from 1 mL of plasma using the QIAamp Circulating Nucleic Acid Kit (Qiagen, Hilden, Germany). All DNAs were eluted in a final volume of 50 μL and stored at − 30 °C. DNAs extracted from plasma were quantified using a Qubit fluorometer (Thermo Fisher Scientific, Waltham, MA, USA).

Next-generation sequencing (NGS)

We performed NGS (Miseq, illumina, Hayward, CA, USA) and deep targeted sequencing for 48 cancer-related genes in the target custom enrichment panel (Integrated DNA Technologies, Inc., Coralville, Iowa, USA). In the present study, geneious prime (Biomatters, Ltd., New Zealand) was used as the bioinformatics tools for the analyses. We set the cut-off value at 1% frequency. In addition to these cut-off values, we set the coverage over 1000. We excluded the genes for which mutations were detected in non-cancerous tissue samples in further analysis.

Droplet digital PCR

The presence of mutations was detected via droplet digital PCR (QX200 system; Bio-Rad Laboratories, Hercules, CA, USA) using each probe that was designed from the results of NGS. The probes used are as follows: TP53 R136H, KIT N818H, BRAF I452S, ERBB2 V812I, ATM L3017R, STK11 L195M, PIK3CA R88Q, STK11 R333C, ERBB2 V812L, TP53 C110W, SMAD4 E330D, AR Y225S, MAP 2 K4 R134Q, PDGFRA F837V, PDGFRA I843S, KRAS G12V, KIT W553C, KIT Y819S, TP53 R150W, ATM L2890I, RUNX1 P403L, TP53 H140Q, MAP 2 K4 S184L, MAP 2 K4 V321M, TP53 R141H, RUNX1 N233T, IDH2 R172G, PDGRFA R558H, AR C612S, and FGFR3 K537E. DNA eluent (5 μL) from plasma was mixed with Droplet PCR Supermix (10 μL; Bio-Rad Laboratories, Hercules, CA, USA), primer/probe mixture (2 μL), and sterile DNase- and RNase-free water (5 μL). The mixture (22 μL) was added to droplet generation oil (70 μL; Bio-Rad Laboratories, Hercules, CA, USA) to produce a droplet. The emulsion was subjected to PCR in a thermal cycler and the conditions were as follows: an initial temperature of 95 °C for 10 min, 40 cycles at 94 °C for 30 s, and 55 °C for 1 min. A final step was performed at 98 °C for 10 min for enzyme deactivation and the reaction mixtures were analyzed using a droplet reader (Bio-Rad Laboratories, Hercules, CA, USA). For quantification, fluorescence signal readout was obtained using QuantaSoft software (Bio-Rad Laboratories, Hercules, CA, USA). In this study, we set the minimum number of events used to call positivity at one droplet, and the threshold of fluorescence intensity at 1200 using a positive control and a negative control, which were artificial gene synthesis products. All experiments were conducted in duplicates to diminish the effect of a false negative result, although its probability was low in these materials. A result was considered positive even if it occurred once.


Patient characteristics

There were eight cases of ulcerative colitis and two cases of Crohn’s disease. The median age of the patients was 49 years, comprising of four males and six females. Out of the 10 patients, seven had IBD-associated cancer and three had high-grade dysplasia. Two patients had carcinoma in situ; moreover, three had stageII and two had stageIII (Table 1).

Table 1 Patient characteristics

The patient background for each of the cases is as follows: cases 1 and 2 have Crohn’s disease; cases 3 to 10 have ulcerative colitis; cases 1 to 5 have advanced cancer; cases 6 to 10 have carcinoma in situ and/or HGD. Tumor DNA mutation analysis was performed on these cases using next-generation sequencers (Table 1).

The NGS analysis

The NGS analysis of tumor tissue DNA showed the following results: in case 1, TP53 was 20.9%; in case 2, PIC3CA was 34.1%; in case 3, TP53 was 25.7%; in case 4, KRAS was 40%; in case 5, TP53 was 31.1%; in case 6, TP53 was 8.5%; in case 7, TP53 was 12.8%; in case 8, IDH2 was 1.1%; in case 9, AR was 1.5%; and in case 10, FGFR3 was 1.0% in frequency (Table 2).

Table 2 The next-generation sequencing and the digital PCR analysis in case 1 to 10

The NGS of control showed that there were no genes more than 3% in frequency (Supplemental 1).

The digital PCR analysis

The following are the results of digital PCR analysis of blood ctDNA: detection of TP53 in case 1, PIC3CA in case 2, TP53 in case 3, KRAS in case 4, TP53 in case 5, TP53 in case 6, and TP53 in case 7. However, we were unable to detect cases 8, 9, and 10, which had low mutation frequencies in tumor tissue DNA. Interestingly, the high frequency of the tumor tissue DNA mutation, especially those with a frequency of 5% or higher, could be detected by blood ctDNA. Amino acid substitutions due to mutations in tissue DNA and blood ctDNA also correlated with each other, thus suggesting that the ctDNA in these cases originated in tumor tissue DNA (Table 2).

If we consider more than 5% of the tumor tissue DNA mutations to be positive, it would result in three wild type and seven mutation cases. For these cases, the results of blood ctDNA detection via liquid biopsy also confirmed three wild type and seven mutation cases. Therefore, the concordance rate was 100% (Table 3).

Table 3 Comparison between tumor tissue DNA and blood ctDNA

Liquid biopsy in ten patients with ulcerative colitis without a tumor showed there was no detected genes (Supplemental 1).


In this study, the detection of blood ctDNA in IBD-associated tumors was performed. The concordance rate between tumor tissue DNA and blood ctDNA was 100%, thereby suggesting the possibility of a non-invasive method. Interestingly, liquid biopsy was also useful for high-grade dysplasia cases, but a certain frequency of tumor tissue DNA mutations was required for the detection of blood ctDNA mutations.

Our previous studies revealed that ctDNA mutations require more than 10% frequency rate of target tumor tissue DNA mutations [15,16,17]. The current results, therefore, corroborated the previous studies. Although cancerous lesions and non-cancerous lesions in patients with IBD had a few types of mutations due to carcinogenesis and inflammation, the key driver mutations had much higher frequency. For this reason, liquid biopsy might be an ideal method because only high frequency mutations could be detected by blood ctDNA.

Although the utility of liquid biopsy has recently been demonstrated in various fields, there have been no reports on detection of IBD-associated neoplasia using this technique. This may be due to the lack of centers that handle large numbers of cases and the need to target a large number of genes. However, this is the first study to report the use of this technique for the detection of IBD-associated neoplasia.

There are few limitations in this study. First, this is a single-center, small-scale, retrospective, observational study, so that a multicenter, large-scale, prospective study will be required. Based on these results, a prospective validation study is underway. Second, the study evaluates only 48 genes and higher detection rate can be achieved by combining other genetic mutations in future studies. Third, the origin of gene mutation in blood is unknown. This hinders the clinical application of liquid biopsy; however, in this study, we compared tumor tissue DNA and blood ctDNA mutations and even confirmed a match between the mutation locations, and therefore, conclude that the ctDNA was derived from cancer tissues. Forth, although DNA is usually stable for long time, we have not examined the effect of the storage time on this analysis. The storage period might be one of the limitations in future studies. Fifth, cfDNA quantity in blood might limit the detection in early stage disease. Sixth, although biopsy samples were not used in this study, laser microdissection might help to capture the dysplastic areas in that case.


Blood liquid biopsy has the potential to be a new method for non-invasive diagnosis of IBD-associated tumors and may develop as one of the next-generation detection techniques in future. Although further molecular biological analysis will be required to narrow down the candidate genes for future use in screening, it could be a very useful method for monitoring.

Availability of data and materials

The datasets used and analysed during the current study are available from the corresponding author on reasonable request.



Inflammatory bowel disease


High-grade dysplasia


Circulating tumor DNA


Narrow band imaging


Formalin fixed paraffin embedded


Cell free DNA


Next-generation sequencing


  1. Eaden JA, Abrams KR, Mayberry JF. The risk of colorectal cancer in ulcerative colitis: a meta-analysis. Gut. 2001;48(4):526–35.

    Article  CAS  Google Scholar 

  2. Rutter MD, Saunders BP, Wilkinson KH, Rumbles S, Schofield G, Kamm MA, Williams CB, Price AB, Talbot IC, Forbes A. Thirty-year analysis of a colonoscopic surveillance program for neoplasia in ulcerative colitis. Gastroenterology. 2006;130(4):1030–8.

    Article  Google Scholar 

  3. Rogler G. Chronic ulcerative colitis and colorectal cancer. Cancer Lett. 2014;345(2):235–41.

    Article  CAS  Google Scholar 

  4. Bye WA, Ma C, Nguyen TM, Parker CE, Jairath V, East JE. Strategies for detecting colorectal cancer in patients with inflammatory bowel disease: a cochrane systematic review and meta-analysis. Am J Gastroenterol. 2018;113(12):1801–9.

    Article  Google Scholar 

  5. Watanabe T, Ajioka Y, Mitsuyama K, Watanabe K, Hanai H, Nakase H, Kunisaki R, Matsuda K, Iwakiri R, Hida N, et al. Comparison of targeted vs random biopsies for surveillance of ulcerative colitis-associated colorectal cancer. Gastroenterology. 2016;151(6):1122–30.

    Article  Google Scholar 

  6. Bisschops R, Bessissow T, Joseph JA, Baert F, Ferrante M, Ballet V, Willekens H, Demedts I, Geboes K, De Hertogh G, et al. Chromoendoscopy versus narrow band imaging in UC: a prospective randomised controlled trial. Gut. 2018;67(6):1087–94.

    Article  Google Scholar 

  7. Moussata D, Allez M, Cazals-Hatem D, Treton X, Laharie D, Reimund JM, Bertheau P, Bourreille A, Lavergne-Slove A, Brixi H, et al. Are random biopsies still useful for the detection of neoplasia in patients with IBD undergoing surveillance colonoscopy with chromoendoscopy? Gut. 2018;67(4):616–24.

    PubMed  Google Scholar 

  8. Beaugerie L, Itzkowitz SH. Cancers complicating inflammatory bowel disease. N Engl J Med. 2015;373(2):195.

    CAS  PubMed  Google Scholar 

  9. Baker AM, Cross W, Curtius K, Al Bakir I, Choi CR, Davis HL, Temko D, Biswas S, Martinez P, Williams MJ, et al. Evolutionary history of human colitis-associated colorectal cancer. Gut. 2019;68(6):985–95.

    Article  CAS  Google Scholar 

  10. Yaeger R, Shah MA, Miller VA, Kelsen JR, Wang K, Heins ZJ, Ross JS, He Y, Sanford E, Yantiss RK, et al. Genomic alterations observed in colitis-associated cancers are distinct from those found in sporadic colorectal cancers and vary by type of inflammatory bowel disease. Gastroenterology. 2016;151(2):278–87 e276.

    Article  CAS  Google Scholar 

  11. Robles AI, Traverso G, Zhang M, Roberts NJ, Khan MA, Joseph C, Lauwers GY, Selaru FM, Popoli M, Pittman ME, et al. Whole-exome sequencing analyses of inflammatory bowel disease-associated colorectal cancers. Gastroenterology. 2016;150(4):931–43.

    Article  CAS  Google Scholar 

  12. Lin YC, Lin YC, Chen CJ. Cancers complicating inflammatory bowel disease. N Engl J Med. 2015;373(2):194–5.

    CAS  PubMed  Google Scholar 

  13. Wan JCM, Massie C, Garcia-Corbacho J, Mouliere F, Brenton JD, Caldas C, Pacey S, Baird R, Rosenfeld N. Liquid biopsies come of age: towards implementation of circulating tumour DNA. Nat Rev Cancer. 2017;17(4):223–38.

    Article  CAS  Google Scholar 

  14. Pantel K, Alix-Panabieres C. Liquid biopsy and minimal residual disease - latest advances and implications for cure. Nat Rev Clin Oncol. 2019;16(7):409–24.

    Article  CAS  Google Scholar 

  15. Kinugasa H, Nouso K, Miyahara K, Morimoto Y, Dohi C, Tsutsumi K, Kato H, Matsubara T, Okada H, Yamamoto K. Detection of K-ras gene mutation by liquid biopsy in patients with pancreatic cancer. Cancer. 2015;121(13):2271–80.

    Article  CAS  Google Scholar 

  16. Kinugasa H, Nouso K, Tanaka T, Miyahara K, Morimoto Y, Dohi C, Matsubara T, Okada H, Yamamoto K. Droplet digital PCR measurement of HER2 in patients with gastric cancer. Br J Cancer. 2015;112(10):1652–5.

    Article  CAS  Google Scholar 

  17. Kinugasa H, Nouso K, Ako S, Dohi C, Matsushita H, Matsumoto K, Kato H, Okada H. Liquid biopsy of bile for the molecular diagnosis of gallbladder cancer. Cancer Biol Ther. 2018;19(10):934–8.

    Article  CAS  Google Scholar 

Download references


We thank all of patients for their participation in the study.


This study was supported by JSPS KAKENHI (19 k17433). The funding bodies played no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.

Author information

Authors and Affiliations



Dr. HK designed and drafted the manuscript. Dr. SH, Dr. EY, Dr. SO, Dr. MO, Dr. YY, Dr. TI, Dr. MT and Dr. KH collected the clinical data. Dr. HK, Dr. SY, Dr. MH and Dr. HT were responsible for experiments. Dr. HK and Dr. TT analyzed the data. Dr. HS, Dr. KN and Dr. HO supervised the manuscript preparation. All authors approved the final manuscript.

Corresponding author

Correspondence to Hideaki Kinugasa.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the Ethics Committee of Okayama University Hospital and all patients provided written informed consent prior to enrolment.

Consent for publication

Not applicable.

Competing interests

The authors declare that there are no conflicts of interest.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Supplemental 1.

The next-generation sequencing and the digital PCR analysis in control 1 to 10 (Crohn: 1–5; UC: 6–10).

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kinugasa, H., Hiraoka, S., Nouso, K. et al. Liquid biopsy for patients with IBD-associated neoplasia. BMC Cancer 20, 1188 (2020).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: