Biomarkers of precancerous diseases of the gastric mucosa in schoolchildren of ethnic populations of Tyva
https://doi.org/10.21518/ms2026-001
Abstract
Introduction. Researchers have focused on identifying biomarkers for the risk of developing precancerous conditions in the gastric mucosa. CDX2, CK20, and CK7 proteins have been linked to precancerous conditions, even in childhood.
Aim. To study the expression of CDX2, CK20, and CK7 proteins in the gastric mucosal epithelium of schoolchildren with gastritis in ethnic populations of the Republic of Tyva.
Materials and methods. A cross-sectional questionnaire survey was conducted among schoolchildren aged 7–17 in Tyva in 2017: 336 Mongoloid Tuvans and 135 Caucasians; 184 boys and 287 girls. Subsequently, children with gastrointestinal complaints underwent gastroscopy: 57 Tuvans of Mongoloid origin and 32 Caucasians (35 boys and 54 girls) with gastric mucosal samples collected and subsequently morphologically confirmed the diagnosis of gastritis. Biopsies were examined immunohistochemically to detect CDX2, CK20, and CK7 proteins in the gastric epithelium.
Results. CDX2 expression was determined only in the epithelium of the antral section in 4 schoolchildren (4.5%) and its differences in ethnic populations were not noted. CK7 expression was observed more often in the antral section of the stomach in Tuvans than in Caucasians (p = 0.038). In both stomach sections, no differences in CK20 expression were observed in children of ethnic populations. In Caucasians, there was a tendency for CK7 expression in the antrum to increase with age (p = 0.092). Whereas in Tuvans, CK7 expression rates in the antrum were high in younger schoolchildren and higher than in Caucasians of the same age (p = 0.022). In the body of the stomach, the expression of CK7 was also higher in Tuvans of the younger age group.
Conclusions. CK20 and CK7 expression patterns can be used as a criterion for identifying children with an increased risk of developing precancerous changes in the stomach and gastric cancer in adulthood.
About the Authors
V. A. VshivkovRussian Federation
Vitaliy A. Vshivkov - Cand. Sci. (Med.), Senior Scientist of Clinical Division of Digestive System Pathology in Adults and Children, Federal Research Center “Krasnoyarsk Science Center” of the Siberian Branch of the Russian Academy of Sciences of Scientific Research Institute of Medical Problems of the North.
3g, Partizan Zheleznyak St., Krasnoyarsk, 660022
T. V. Polivanova
Russian Federation
Tamara V. Polivanova - Dr. Sci. (Med.), Chief Researcher of Clinical Division of Digestive System Pathology in Adults and Children, Federal Research Center “Krasnoyarsk Science Center” of the Siberian Branch of the Russian Academy of Sciences of Scientific Research Institute of Medical Problems of the North; Professor of the Department of Pathological Physiology of the Krasnoyarsk State Medical University named after Professor V.F. Voino-Yasenetsky.
3g, Partizan Zheleznyak St., Krasnoyarsk, 660022; 1, Partizan Zheleznyak St., Krasnoyarsk, 660022
E. V. Kasparov
Russian Federation
Eduard V. Kasparov - Dr. Sci. (Med.), Professor, Director, Federal Research Center “Krasnoyarsk Science Center” of the Siberian Branch of the Russian Academy of Sciences of Scientific Research Institute of Medical Problems of the North.
3g, Partizan Zheleznyak St., Krasnoyarsk, 660022
References
1. George S, Lucero Y, Torres JP, Lagomarcino AJ, O’Ryan M. Gastric Damage and Cancer-Associated Biomarkers in Helicobacter pylori-Infected Children. Front Microbiol. 2020;11:90. https://doi.org/10.3389/fmicb.2020.00090.
2. Negovan A, Iancu M, Fülöp E, Bănescu C. Helicobacter pylori and cytokine gene variants as predictors of premalignant gastric lesions. World J Gastroenterol. 2019;25(30):4105–4124. https://doi.org/10.3748/wjg.v25.i30.4105.
3. Kumar S, Patel GK, Ghoshal UC. Helicobacter pylori-Induced Inflammation: Possible Factors Modulating the Risk of Gastric Cancer. Pathogens. 2021;10(9):1099. https://doi.org/10.3390/pathogens10091099.
4. Toh JWT, Wilson RB. Pathways of Gastric Carcinogenesis, Helicobacter pylori Virulence and Interactions with Antioxidant Systems, Vitamin C and Phytochemicals. Int J Mol Sci. 2020;21(17):6451. https://doi.org/10.3390/ijms21176451.
5. Díaz Del Arco C, Fernández Aceñero MJ, Ortega Medina L. Liquid biopsy for gastric cancer: Techniques, applications, and future directions. World J Gastroenterol. 2024;30(12):1680–1705. https://doi.org/10.3748/wjg.v30.i12.1680.
6. Mithany RH, Shahid MH, Manasseh M, Saeed MT, Aslam S, Mohamed MS et al. Gastric Cancer: A Comprehensive Literature Review. Cureus. 2024;16(3):e55902. https://doi.org/10.7759/cureus.55902.
7. Pattilachan TM, Christodoulou M, Ross S. Diagnosis to dissection: AI’s role in early detection and surgical intervention for gastric cancer. J Robot Surg. 2024;18(1):259. https://doi.org/10.1007/s11701-024-02005-6.
8. Melkonian SC, Jim MA, Reza A, Peipins LA, Haverkamp D, Said N et al. Incidence of Stomach, Liver, and Colorectal Cancers by Geography and Social Vulnerability Among American Indian and Alaska Native Populations, 2010-2019. Am J Epidemiol. 2024;193(1):58–74. https://doi.org/10.1093/aje/kwad194.
9. Spees LP, Jackson BE, Raveendran Y, Morris HN, Emerson MA, Baggett CD et al. Characterizing Cancer Burden in the American Indian Population in North Carolina. Cancer Epidemiol Biomarkers Prev. 2024;33(6):838–845. https://doi.org/10.1158/1055-9965.EPI-24-0030.
10. Bair MJ, Chuang SL, Lei WY, Chen CL, Tian HW, Chiang TH et al. Planning mass eradication of Helicobacter pylori infection for indigenous Taiwanese peoples to reduce gastric cancer. J Gastroenterol Hepatol. 2020;35(4):609–616. https://doi.org/10.1111/jgh.14898.
11. Moore SP, Forman D, Piñeros M, Fernández SM, de Oliveira Santos M, Bray F. Cancer in indigenous people in Latin America and the Caribbean: a review. Cancer Med. 2014;3(1):70–80. https://doi.org/10.1002/cam4.134.
12. Chief C, Sanderson PR, Willeto AAA, Yazzie A, McKinley A, Monroy FP et al. “Nobody Is Talking About It”: Diné (Navajo) Communities Speak About Stomach Cancer and Helicobacter pylori Infections. J Cancer Educ. 2022;37(1):3–9. https://doi.org/10.1007/s13187-020-01831-0.
13. Axel EM. Gastrointestinal cancer statistics. Siberian Journal of Oncology. 2017;16(3):5–11. (In Russ.) https://doi.org/10.21294/1814-4861-2017-3-5-11.
14. Vshivkov VA, Polivanova TV, Kasparov EV, Peretyatko OV, Akhmetshin TN. The state of the mucosa of the gastroduodenal zone in schoolchildren residing in areas with a high prevalence rate of gastric cancer. Russian Pediatric Journal. 2018;21(1):26–30. (In Russ.) https://doi.org/10.18821/1560-9561-2018-21-1-26-30.
15. Machlowska J, Baj J, Sitarz M, Maciejewski R, Sitarz R. Gastric Cancer: Epidemiology, Risk Factors, Classification, Genomic Characteristics and Treatment Strategies. Int J Mol Sci. 2020;21(11):4012. https://doi.org/10.3390/ijms21114012.
16. Koulis A, Buckle A, Boussioutas A. Premalignant lesions and gastric cancer: Current understanding. World J Gastrointest Oncol. 2019;11(9):665–678. https://doi.org/10.4251/wjgo.v11.i9.665.
17. Cordova-Marks FM, Carson WO, Monetathchi A, Little A, Erdrich J. Native and Indigenous Populations and Gastric Cancer: A Worldwide Review. Int J Environ Res Public Health. 2022;19(9):5437. https://doi.org/10.3390/ijerph19095437.
18. Nolen LD, Vindigni SM, Parsonnet J; Symposium leaders. Combating Gastric Cancer in Alaska Native People: An Expert and Community Symposium. Gastroenterology. 2020;158(5):1197–1201. https://doi.org/10.1053/j.gastro.2019.11.299.
19. Němejcová K, Šafanda A, Bártů MK, Michálková R, Drozenová J, Fabian P et al. A comprehensive immunohistochemical analysis of 26 markers in 250 cases of serous ovarian tumors. Diagn Pathol. 2023;18(1):32. https://doi.org/10.1186/s13000-023-01317-9.
20. Villarreal-Calderon R, Luévano-González A, Aragón-Flores M, Zhu H, Yuan Y, Xiang Q et al. Antral atrophy, intestinal metaplasia, and preneoplastic markers in Mexican children with Helicobacter pylori-positive and Helicobacter pylori-negative gastritis. Ann Diagn Pathol. 2014;18(3):129–135. https://doi.org/10.1016/j.anndiagpath.2014.02.003.
21. Todorovic V, Sokic-Milutinovic A, Drndarevic N, Micev M, Mitrovic O, Nikolic I et al. Expression of cytokeratins in Helicobacter pylori-associated chronic gastritis of adult patients infected with cagA+ strains: an immunohistochemical study. World J Gastroenterol. 2006;12(12):1865–1873. https://doi.org/10.3748/wjg.v12.i12.1865.
22. Wang YK, Ran DM, Li YY, Zhu CY, Zhang RB, Jiang B et al. Histopathological features of glandular atrophy of the lamina propria of the gastric mucosa during its occurrence and development. BMC Gastroenterol. 2023;23(1):395. https://doi.org/10.1186/s12876-023-03033-6.
23. Smyth EC, Nilsson M, Grabsch HI, van Grieken NC, Lordick F. Gastric cancer. Lancet. 2020;396(10251):635–648. https://doi.org/10.1016/S0140-6736(20)31288-5.
24. He J, Hu W, Ouyang Q, Zhang S, He L, Chen W et al. Helicobacter pylori infection induces stem cell-like properties in Correa cascade of gastric cancer. Cancer Lett. 2022;542:215764. https://doi.org/10.1016/j.canlet.2022.215764.
25. Dixon MF, Genta RM, Yardley JH. Histological classification of gastritis and Helicobacter pylori infection: an agreement at last? The International Workshop on the Histopathology of Gastritis. Helicobacter. 1997;2(1):17–24. https://doi.org/10.1111/j.1523-5378.1997.06b09.x.
26. Sugano K, Tack J, Kuipers EJ, Graham DY, El-Omar EM, Miura S et al. Kyoto global consensus report on Helicobacter pylori gastritis. Gut. 2015;64(9):1353–1367. https://doi.org/10.1136/gutjnl-2015-309252.
27. Polivanova TV, Kasparov EV, Vshivkov VA, Peretyatko OV. Biomarkers CDX2, CK20, CK7 in Schoolchildren with Gastritis in the Realization of Familial Predisposition of Stomach Cancer. Bull Exp Biol Med. 2021;172(2):187–190. https://doi.org/10.1007/s10517-021-05360-8.
28. Petrovchich I, Ford JM. Genetic predisposition to gastric cancer. Semin Oncol. 2016;43(5):554–559. https://doi.org/10.1053/j.seminoncol.2016.08.006.
29. Yusefi AR, Bagheri Lankarani K, Bastani P, Radinmanesh M, Kavosi Z. Risk Factors for Gastric Cancer: A Systematic Review. Asian Pac J Cancer Prev. 2018;19(3):591–603. https://doi.org/10.22034/APJCP.2018.19.3.591.
30. Luo HT, Liang CX, Luo RC, Gu WG. Identification of relevant prognostic values of cytokeratin 20 and cytokeratin 7 expressions in lung cancer. Biosci Rep. 2017;37(6):BSR20171086. https://doi.org/10.1042/BSR20171086.
31. Yun SP, Seo HI. Prognostic impact of immunohistochemical expression of CK7 and CK20 in curatively resected ampulla of Vater cancer. BMC Gastroenterol. 2015;15:165. https://doi.org/10.1186/s12876-015-0396-x.
Review
For citations:
Vshivkov VA, Polivanova TV, Kasparov EV. Biomarkers of precancerous diseases of the gastric mucosa in schoolchildren of ethnic populations of Tyva. Meditsinskiy sovet = Medical Council. 2026;(1):300-305. (In Russ.) https://doi.org/10.21518/ms2026-001
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