Salivary Fusobacterium nucleatum serves as a potential diagnostic biomarker for gastric cancer
Open accessAbstract
BACKGROUND: (Fn) primarily colonized in the oral cavity, has been reported to be involved in the development of gastrointestinal tumor. Until now, little is known about the relationship between salivary Fn and GC. AIM: To determine whether salivary Fn could be a biomarker to diagnose GC and explore the influence of Fn on GC cells. METHODS: The abundance of Fn in saliva was quantified by droplet digital polymerase chain reaction in 120 GC patients, 31 atrophic gastritis (AG) patients, 35 non-AG (NAG) patients, 26 gastric polyp (GP) patients, and 20 normal controls (NC) from Qilu Hospital of Shandong University from January 2019 to December 2020. Receiver operating characteristic (ROC) curve analysis was performed to evaluate the diagnostic value of Fn as well as traditional serum tumor markers, including carcinoembryonic antigen (CEA), carbohydrate antigen (CA) 19-9, and CA72-4. Transwell assay and wound-healing assay were conducted to assess the influence of Fn infection on GC cells. The expression of epithelial-mesenchymal transition (EMT) markers was detected using western blot assay. RESULTS: < 0.001). ROC curve analysis showed a favorable capability of Fn (73.33% sensitivity; 82.14% specificity; area under the curve: 0.813) in GC diagnosis, which was superior to that of CEA, CA19-9, CA72-4, ferritin, and sialic acid. The Fn level in saliva of GC patients was increased as the TNM stage increased. GC patients with lymph node metastasis had higher Fn levels than those without metastasis. Both transwell and wound-healing assays indicated that Fn infection promoted the migration and invasion of GC cells. Western blot analysis showed that Fn infection decreased the expression of E-cadherin and increased the expressions of N-cadherin, vimentin, and snail. CONCLUSION: Fn abundance in saliva could be used as a promising biomarker to diagnose GC, and Fn infection could promote GC metastasis by accelerating the EMT process.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Based on reported target strain abundance in saliva (<10^7 cells/mL for each target species) and average saliva volume, the total amount of postbiotic cells required for efficient coaggregation was estimated to be 10^9 bacterial cells/g of product.
“Based on the reported target strain abundance in saliva (<107 cells/mL saliva for each of the target species) [43–46] and the average saliva volume in the mouth under stimulated conditions [47,48], we estimated that the total amount of postbiotic cells required for efficient coaggregation would be 109 bacterial cells/g of product.”
From Coaggregation of oral pathogens by postbiotic lactobacilli (2025) · cites this paper as [45]
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Bray, F., Ferlay, J., Soerjomataram, I., Siegel, R. L., Torre, L. A., & Jemal, A. (2018) · CA: A Cancer Journal for Clinicians · doi:10.3322/caac.21492 · Cited by 84,109 · see citing works
Unidentified curved bacilli in the stomach of patients with gastritis and peptic ulceration
Marshall, B., & Warren, J. R. (1984) · The Lancet · doi:10.1016/s0140-6736(84)91816-6 · Cited by 5,509 · see citing works
Defining the normal bacterial flora of the oral cavity
Aas, J. A., Paster, B. J., Stokes, L. N., Olsen, I., & Dewhirst, F. E. (2005) · Journal of Clinical Microbiology · doi:10.1128/jcm.43.11.5721-5732.2005 · Cited by 3,092 · see citing works
Rubinstein, M. R., Wang, X., Liu, W., Hao, Y., Cai, G., & Han, Y. W. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.07.012 · Cited by 2,476 · see citing works
Fusobacterium nucleatum Promotes Chemoresistance to Colorectal Cancer by Modulating Autophagy
Yu, T., Guo, F., Yu, Y., Sun, T., Ma, D., Han, J., Qian, Y., Kryczek, I., Sun, D., Nagarsheth, N., et al. (2017) · Cell · doi:10.1016/j.cell.2017.07.008 · Cited by 2,198 · see citing works
Occlusal Caries: Biological Approach for Its Diagnosis and Management
Carvalho, J. C., Dige, I., Mačhiulskienė, V., Qvist, V., Bakhshandeh, A., Parolo, C. C. F., & Maltz, M. (2016) · Caries Research · doi:10.1159/000448662 · Cited by 2,159 · see citing works
Analysis of <i>Fusobacterium</i> persistence and antibiotic response in colorectal cancer
Bullman, S., Pedamallu, C. S., Sicinska, E., Clancy, T. E., Zhang, X., Cai, D., Neuberg, D., Huang, K., Guevara, F., Nelson, T., et al. (2017) · Science · doi:10.1126/science.aal5240 · Cited by 1,574 · see citing works
Self-citationGur, C., Ibrahim, Y., Isaacson, B., Yamin, R., Abed, J., Gamliel, M., Enk, J., Bar-On, Y., Stanietsky-Kaynan, N., Coppenhagen-Glazer, S., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.01.010 · Cited by 1,490 · see citing works
The bacteria of periodontal diseases
Moore, W. E., & Moore, L. V. H. (1994) · Periodontology 2000 · doi:10.1111/j.1600-0757.1994.tb00019.x · Cited by 1,077 · see citing works
Fusobacterium nucleatum: a commensal-turned pathogen
Han, Y. W. (2015) · Current Opinion in Microbiology · doi:10.1016/j.mib.2014.11.013 · Cited by 832 · see citing works
Epithelial–mesenchymal transition in tumor metastasis
Yeung, K. T., & Yang, J. (2016) · Molecular Oncology · doi:10.1002/1878-0261.12017 · Cited by 724 · see citing works
Diagnostic and prognostic value of CEA, CA19–9, AFP and CA125 for early gastric cancer
Feng, F., Tian, Y., Xu, G., et al. (2017) · BMC Cancer · doi:10.1186/s12885-017-3738-y · Cited by 374 · see citing works
Zhang, S., Yang, Y. P., Weng, W., Guo, B., Cai, G., Ma, Y., & Cai, S. (2019) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-018-0985-y · Cited by 318 · see citing works
Fardini, Y., Wang, X., Témoin, S., Nithianantham, S., Lee, D. M., Shoham, M., & Han, Y. W. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07905.x · Cited by 292 · see citing works
Term Stillbirth Caused by Oral Fusobacterium nucleatum
Han, Y. W., Fardini, Y., Chen, C., Iacampo, K. G., Peraino, V. A., Shamonki, J. M., & Redline, R. W. (2010) · Obstetrics & Gynecology · doi:10.1097/aog.0b013e3181cb9955 · Cited by 289 · see citing works
Hsieh, Y.-Y., Tung, S.-Y., Pan, H.-Y., Yen, C.-W., Xu, H.-W., Lin, Y.-J., Deng, Y.-F., Hsu, W.-T., Wu, C.-S., & Li, C. (2018) · Scientific Reports · doi:10.1038/s41598-017-18596-0 · Cited by 269 · see citing works
Abed, J., Maalouf, N., Manson, A. L., Earl, A. M., Parhi, L., Emgård, J., Klutstein, M., Tayeb, S., Almogy, G., Atlan, K., et al. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00400 · Cited by 269 · see citing works
<i>Fusobacterium nucleatum</i>and colorectal cancer: A review
Shang, F.-M., & Liu, H.-L. (2018) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v10.i3.71 · Cited by 258 · see citing works
Fusobacterium nucleatum promotes colorectal cancer metastasis by modulating KRT7-AS /KRT7
Chen, S., Su, T., Zhang, Y., Lee, A. A., He, J., Ge, Q., Wang, L., Si, J., Zhuo, W., & Wang, L. (2020) · Gut Microbes · doi:10.1080/19490976.2019.1695494 · Cited by 232 · see citing works
Self-citationChen, Y., Chen, Y., Zhang, J., Cao, P., Su, W., Deng, Y., Zhan, N., Fu, X., Huang, Y., & Dong, W. (2019) · Theranostics · doi:10.7150/thno.38870 · Cited by 190 · see citing works
Wang, X., Buhimschi, C. S., Témoin, S., Bhandari, V., Han, Y. W., & Buhimschi, I. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056131 · Cited by 189 · see citing works
Rasiah, I. A., Wong, L., Anderson, S. A., & Sissons, C. H. (2005) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2005.02.001 · Cited by 131 · see citing works
Yan, X., Liu, L., Li, H., Qin, H., & Sun, Z. (2017) · OncoTargets and Therapy · doi:10.2147/ott.s145949 · Cited by 110 · see citing works
Ianiro, G., Molina‐Infante, J., & Gasbarrini, A. (2015) · Helicobacter · doi:10.1111/hel.12260 · Cited by 87 · see citing works
Yu, M. R., Kim, H. J., & Park, H. R. (2020) · Cancers · doi:10.3390/cancers12102728 · Cited by 86 · see citing works
Impact of the Microbiota and Gastric Disease Development by Helicobacter pylori
Alarcón, T., Llorca, L., & Perez-Perez, G. (2017) · Current topics in microbiology and immunology · doi:10.1007/978-3-319-50520-6_11 · Cited by 72 · see citing works
Kabwe, M., Brown, T. L., Dashper, S. G., Speirs, L. B. M., Ku, H., Petrovski, S., Chan, H. T., Lock, P., & Tucci, J. (2019) · Scientific Reports · doi:10.1038/s41598-019-45549-6 · Cited by 70 · see citing works
Hutton, M. L., Kaparakis‐Liaskos, M., Turner, L., Cardona, A., Kwok, T., & Ferrero, R. L. (2010) · Infection and Immunity · doi:10.1128/iai.00439-10 · Cited by 68 · see citing works
Fragkioudakis, I., Riggio, M., & Apatzidou, D. (2020) · Journal of Medical Microbiology · doi:10.1099/jmm.0.001247 · Cited by 55 · see citing works
Hsieh, Y., Tung, S., Pan, H.-Y., Chang, T., Wei, K., Chen, W., Deng, Y.-F., Lu, C.-K., Lai, Y., Wu, C., et al. (2021) · World Journal of Gastroenterology · doi:10.3748/wjg.v27.i42.7311 · Cited by 50 · see citing works
Self-citationSekiguchi, M., & Matsuda, T. (2020) · Scientific Reports · doi:10.1038/s41598-020-75319-8 · Cited by 49 · see citing works
Complex Intratissue Microbiota Forms Biofilms in Periodontal Lesions
Baek, K. J., Ji, S., & Choi, Y. (2017) · Journal of Dental Research · doi:10.1177/0022034517732754 · Cited by 45 · see citing works
Nozawa, A., Oshima, H., Togawa, N., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0229485 · Cited by 26 · see citing works
Fusobacterium nucleatum produces cancer stem cell characteristics via EMT-resembling variations.
Wang, Q. L., Chen, Y., Yue, C., & Liu, X. (2020) · PubMed Central · Cited by 21 · see citing works
MACC1 and HGF are associated with survival in patients with gastric cancer
Dong, G., Wang, M., Gu, G., et al. (2017) · Oncology Letters · doi:10.3892/ol.2017.7710 · Cited by 15 · see citing works
L‑fucose ameliorates the carcinogenic properties of Fusobacterium nucleatum in colorectal cancer
Duan, C., Tang, X., Wang, W., Qian, W., Fu, X., Deng, X., Han, C., & Hou, X. (2020) · Oncology Letters · doi:10.3892/ol.2020.12404 · Cited by 14 · see citing works
Habib, A. M., Islam, M. S., Sohel, M., Mazumder, M. H. H., Sikder, M. O. F., & Shahik, S. M. (2016) · Genomics & Informatics · doi:10.5808/gi.2016.14.4.255 · Cited by 5 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Coaggregation of oral pathogens by postbiotic lactobacilli
Golletz, P., Jensen, S. D., Collignon, M., Hall, C., Khamas, A. B., Møllebjerg, A., Schlafer, S., Meyer, R. L., & Tykwinska, K. (2025) · Journal of oral microbiology · doi:10.1080/20002297.2025.2508483 · Cited by 10 · see citing works
- Authors
- Chen, W.-D., Zhang, X., Zhang, M.-J., Zhang, Y.-P., Shang, Z.-Q., Xin, Y.-W., & Zhang, Y.
- Affiliations
- Qilu Hospital of Shandong University (CN)
- ORCID
- Venue
- World Journal of Gastroenterology
- Publisher
- Baishideng Publishing Group Inc.
- Published
- 2022-08-14
- Volume
- 28
- Issue
- 30
- Pages
- 4120-4132
- ISSN
- 1007-9327 (ISSN-L)
- PMC
- PMC9403436
- OpenAlex
- W4292451879
- Cited by
- 38
- References
- 37
- Citations by year
- 2026: 7 · 2025: 11 · 2024: 9 · 2023: 10 · 2022: 1
- FWCI
- 7.41
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by-nc
- Locations
- World Journal of Gastroenterology (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Surgery › Helicobacter pylori-related gastroenterology studies
- Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Gastric Cancer Management and Outcomes
- Keywords
- Fusobacterium nucleatum, gastric cancer, salivary biomarkers, diagnostic biomarkers, epithelial-mesenchymal transition, tumor cell migration and invasion, lymph node metastasis, atrophic gastritis, serum tumor markers, E-cadherin, N-cadherin, vimentin, snails
- MeSH terms
- Carcinoembryonic Antigen, Ferritins, Humans, Prognosis, Stomach Neoplasms, Biomarkers, Tumor, Vimentin, Cadherins, Fusobacterium nucleatum, Adenomatous Polyps, CA-19-9 Antigen, N-Acetylneuraminic Acid
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review