إرتباط محركات الخلية الالتهابية القوية بالمؤشرات الحيوية لتلف الحمض النووي المؤكسد في مرضى سرطان المعدة

المؤلفون

  • Akam Jasim Mustafa قسم الكیمیاء، فاكلتي العلوم، جامعة سوران، اربيل ،العراق https://orcid.org/0000-0002-3759-3132
  • بروین عبدالصمد اسماعیل قسم الكیمیاء، كلية التربية، جامعة صلاح الدین، اربيل ،العراق https://orcid.org/0000-0002-2410-4889

DOI:

https://doi.org/10.21123/bsj.2022.6589

الكلمات المفتاحية:

سرطان المعدة، السيتوكينات الالتهابية، الإجهاد التأكسدي، تلف الحمض النووي التأكسدي

الملخص

تحفز الإصابة بالبكتيريا الحلزونية سلسلة إشارات تؤدي إلى إنتاج السيتوكينات وتسبب الإجهاد التأكسدي، الذي يشارك في الاستجابة الالتهابية المزمنة التي تؤدي إلى الإصابة بسرطان المعدة. تنتج أنواع الأكسجين التفاعلية (ROS). 8-Hydroxydeoxyguanosine (8-OHdG) منتج متلف الحمض النووي المؤكسد المستمر. الغرض من الدراسة هو تقييم الارتباط بين مستويات السيتوكينات الالتهابية ووجود تلف الحمض النووي المؤكسد في مرضى المصابين بسرطان المعدة. بالإضافة إلى ذلك، تم إجراء تقييم للقيمة التشخيصية والإنذارية لتلف الحمض النووي المؤكسد والمؤشرات الحيوية السيتوكينية الالتهابية لسرطان المعدة. أجريت الدراسة على مرضى سرطان المعدة الذين تم تشخيصهم طبيا قبل اخذ العلاج. حيث تم اختيار 33 مريضا من المصابين بسرطان المعدة وتقسيمهم إلى المراحل الأولى والثانية والثالثة وفقا لعلم الأمراض السريرية، و32 فردا من الأشخاص الأصحاء المتطابقين مع العمر كمجموعة ضابطة. تم قياس مستوى كل من (8-OHdG)، السيتوكينات (IL-6، TNF-α،IFN-γ, CEA). أظهرت النتائج ارتفاعً بشكل ملحوظ (P<0.0001) في مستويات الدم كل من 8-OHdG وTNF-α وIFN-γ ارتفاعً بشكل غير ملحوظ (IL-6) (P=0.4747) في مرضى GC بالمقارنة بالمجموعة ضابطة، مع زيادة المستويات تدريجياً مع تقدم مراحل المرض. علاوة على ذلك، كان هناك ارتباط إيجابي ضئيل (P=0.3472) (r=0.12 بين مستويات 8-OHdG وIL-6، وارتباط إيجابي ملحوظ (P<0.0001) (r=0.7235) بين مستويات 8-OHdG, TNF-α, CEA,. في مرضى سرطان المعدة ومع ذلك، كان هناك ارتباط سلبي ضئيل (P= 0.6342) (r=-0.06559) بين مستويات 8-OHdG وIFN-γ. تظهر نتائج الدراسة الحالية وجود صلة قوية بين مستويات مصل 8-OHdG والسيتوكينات الالتهابية في مرضى GC. تشير الزيادة المعنوية في تلف الحمض النووي المؤكسد والمؤشرات الحيوية للسيتوكينات الالتهابي وCEA في الدم إلى أن الإجهاد التأكسدي والالتهاب المزمن متضمنان في تسرطن المعدة. تهدف هذه الملاحظات إلى أن 8-OHdG وTNF-α وIFN-γ هي مؤشرات حيوية قابلة للتطبيق لتشخيص ورم المعدة.

المراجع

Galadari S, Rahman A, Pallichankandy S, Thayyullathil F. Reactive oxygen species and cancer paradox: To promote or to suppress? Free Radic Biol Med. 2017;104:144-64.

Basu AK. DNA Damage, Mutagenesis and Cancer. Int J Mol Sci. 2018;19(4):970.

Klaunig JE. Oxidative Stress and Cancer. Curr Pharm Des. 2018;24(40):4771-78.

Whitaker AM, Schaich MA, Smith MR, Flynn TS, Freudenthal BD. Base excision repair of oxidative DNA damage: from mechanism to disease. Front Biosci (Landmark Ed). 2017;22:1493-522.

Al-Taie A, Sancar M, Izzettin FV. Chapter 17 - 8-Hydroxydeoxyguanosine: A valuable predictor of oxidative DNA damage in cancer and diabetes mellitus. In: Preedy VR, Patel VB, editors. Cancer (Second Edition). San Diego: Academic Press; 2021. p. 179-87.

Ferlay J, Colombet M, Soerjomataram I, Mathers C, Parkin DM, Pineros M, et al. Estimating the global cancer incidence and mortality in 2018: GLOBOCAN sources and methods. Int J Cancer. 2019;144(8):1941-53.

Park JY, Forman D, Waskito LA, Yamaoka Y, Crabtree JE. Epidemiology of Helicobacter pylori and CagA-Positive Infections and Global Variations in Gastric Cancer. Toxins. 2018;10(4):163.

Chmiela M, Karwowska Z, Gonciarz W, Allushi B, Stączek P. Host pathogen interactions in Helicobacter pylori related gastric cancer. World J Gastroenterol. 2017;23(9):1521-40.

Díaz P, Valenzuela Valderrama M, Bravo J, Quest AF. Helicobacter pylori and gastric cancer: adaptive cellular mechanisms involved in disease progression. Front Microbiol. 2018;9:5.

Khadem-Ansari M-H, Nozari S, Asoudeh M, Rasmi Y, Faridvand Y. Elevated serum 8-hydroxy-2’-deoxyguanosine, nitrite, and nitrate in patients with stage I multiple myeloma. Int J Cancer Manag. 2017;10(10).

Karki K, Pande D, Negi R, Khanna RS, Khanna HD. An Assessment of Oxidative Damage and Non-Enzymatic Antioxidants Status Alteration in Relation to Disease Progression in Breast Diseases. Med Sci (Basel). 2016;4(4):17.

Borrego S, Vazquez A, Dasí F, Cerdá C, Iradi A, Tormos C, et al. Oxidative stress and DNA damage in human gastric carcinoma: 8-Oxo-7'8-dihydro-2'-deoxyguanosine (8-oxo-dG) as a possible tumor marker. Int J Mol Sci. 2013;14(2):3467-86.

Mazlumoglu MR, Ozkan O, Alp HH, Ozyildirim E, Bingol F, Yoruk O, et al. Measuring oxidative DNA damage with 8-hydroxy-2’-deoxyguanosine levels in patients with laryngeal cancer. Ann Otol Rhinol Laryngol. 2017;126(2):103-09.

Guo C, Li X, Wang R, Yu J, Ye M, Mao L, et al. Association between oxidative DNA damage and risk of colorectal cancer: sensitive determination of urinary 8-hydroxy-2′-deoxyguanosine by UPLC-MS/MS analysis. Sci Rep. 2016;6(1):1-9.

Qing X, Shi D, Lv X, Wang B, Chen S, Shao Z. Prognostic significance of 8-hydroxy-2'-deoxyguanosine in solid tumors: a meta-analysis. BMC Cancer. 2019;19(1):997.

Butcher LD, den Hartog G, Ernst PB, Crowe SE. Oxidative Stress Resulting From Helicobacter pylori Infection Contributes to Gastric Carcinogenesis. Cell Mol Gastroenterol Hepatol. 2017;3(3):316-22.

Kawanishi S, Ohnishi S, Ma N, Hiraku Y, Murata M. Crosstalk between DNA damage and inflammation in the multiple steps of carcinogenesis. Int J Mol Sci. 2017;18(8):1808.

Fu L, Xie C. A lucid review of Helicobacter pylori-induced DNA damage in gastric cancer. Helicobacter. 2019;24(5):e12631.

Gönenç A, Hacışevki A, Aslan S, Torun M, Şimşek B. Increased oxidative DNA damage and impaired antioxidant defense system in patients with gastrointestinal cancer. Eur J Intern Med. 2012;23(4):350-54.

Diakowska D, Lewandowski A, Kopec W, Diakowski W, Chrzanowska T. Oxidative DNA damage and total antioxidant status in serum of patients with esophageal squamous cell carcinoma. Hepatogastroenterology. 2007;54(78):1701-4.

Kubo N, Morita M, Nakashima Y, Kitao H, Egashira A, Saeki H, et al. Oxidative DNA damage in human esophageal cancer: clinicopathological analysis of 8-hydroxydeoxyguanosine and its repair enzyme. Dis Esophagus. 2014;27(3):285-93.

Crohns M, Saarelainen S, Erhola M, Alho H, Kellokumpu-Lehtinen P. Impact of radiotherapy and chemotherapy on biomarkers of oxidative DNA damage in lung cancer patients. Clin Biochem. 2009;42(10-11):1082-90.

Cao C, Lai T, Li M, Zhou H, Lv D, Deng Z, et al. Smoking-promoted oxidative DNA damage response is highly correlated to lung carcinogenesis. Oncotarget. 2016;7(14):18919.

Wei YC, Zhou FL, He DL, Bai JR, Hui LY, Wang XY, et al. The level of oxidative stress and the expression of genes involved in DNA-damage signaling pathways in depressive patients with colorectal carcinoma. J Psychosom Res. 2009;66(3):259-66.

Cobanoglu U, Demir H, Cebi A, Sayir F, Alp HH, Akan Z, et al. Lipid peroxidation, DNA damage and coenzyme Q10 in lung cancer patients--markers for risk assessment? Asian Pac J Cancer Prev. 2011;12(6):1399-403.

Erturk K, Tastekin D, Serilmez M, Bilgin E, Bozbey HU, Vatansever S. Clinical significance of serum interleukin-29, interleukin-32, and tumor necrosis factor alpha levels in patients with gastric cancer. Tumour Biol. 2016;37(1):405-12.

Xu T, Kong Z, Zhao H. Relationship between tumor necrosis factor-α rs361525 polymorphism and gastric cancer risk: A meta-analysis. Front physiol. 2018;9:469.

Zheng W, Zhang S, Zhang S, Min L, Wang Y, Xie J, et al. The relationship between tumor necrosis factor-alpha polymorphisms and gastric cancer risk: An updated meta-analysis. Biomed Rep. 2017;7(2):133-42.

Yan Y, Yu Z, Lu J, Jin P, Tang Z, Hu Y. Predictive values profiling of interleukin-2, interleukin-8, tumor necrosis factor-alpha, procalcitonin, and C-reactive protein in critical gastrointestinal cancer patients. J Gastrointest Oncol. 2021;12(4):1398-406.

Jain SS, Bird RP. Elevated expression of tumor necrosis factor-alpha signaling molecules in colonic tumors of Zucker obese (fa/fa) rats. Int J Cancer. 2010;127(9):2042-50.

Gambhir S, Vyas D, Hollis M, Aekka A, Vyas A. Nuclear factor kappa B role in inflammation associated gastrointestinal malignancies. World J Gastroenterol. 2015;21(11):3174-83.

Cruceriu D, Baldasici O, Balacescu O, Berindan-Neagoe I. The dual role of tumor necrosis factor-alpha (TNF-alpha) in breast cancer: molecular insights and therapeutic approaches. Cell Oncol (Dordr). 2020;43(1):1-18.

Mahdavi Sharif P, Jabbari P, Razi S, Keshavarz-Fathi M, Rezaei N. Importance of TNF-alpha and its alterations in the development of cancers. Cytokine. 2020;130:155066.

Deryugina EI, Soroceanu L, Strongin AY. Up-regulation of vascular endothelial growth factor by membrane-type 1 matrix metalloproteinase stimulates human glioma xenograft growth and angiogenesis. Cancer Res. 2002;62(2):580-8.

Chuang MJ, Sun KH, Tang SJ, Deng MW, Wu YH, Sung JS, et al. Tumor-derived tumor necrosis factor-alpha promotes progression and epithelial-mesenchymal transition in renal cell carcinoma cells. Cancer Sci. 2008;99(5):905-13.

Wang X, Lin Y. Tumor necrosis factor and cancer, buddies or foes? Acta Pharmacol Sin. 2008;29(11):1275-88.

Zhao C, Lu X, Bu X, Zhang N, Wang W. Involvement of tumor necrosis factor-alpha in the upregulation of CXCR4 expression in gastric cancer induced by Helicobacter pylori. BMC Cancer. 2010;10(1):419.

Senthilkumar C, Niranjali S, Jayanthi V, Ramesh T, Devaraj H. Molecular and histological evaluation of tumor necrosis factor-alpha expression in Helicobacter pylori-mediated gastric carcinogenesis. J Cancer Res Clin Oncol. 2011;137(4):577-83.

Bounder G, Jouimyi MR, Boura H, Jouhadi H, Badre W, Benomar H, et al. Association of Tumor Necrosis Factor Receptor 1 Promoter Gene Polymorphisms (-580 A/G and-609 G/T) and TNFR1 Serum Levels with the Susceptibility to Gastric Precancerous Lesions and Gastric Cancer Related to H. pylori Infection in a Moroccan Population. Biomed Res Int. 2020;1(2451854):1-7.

Lee J, Park KH, Ryu JH, Bae HJ, Choi A, Lee H, et al. Natural killer cell activity for IFN-gamma production as a supportive diagnostic marker for gastric cancer. Oncotarget. 2017;8(41):70431.

Zhao H, Dong N, Liu T, Zhang P, Zheng Y, Yang L, et al. Clinical Significance of Serum Type III Interferons in Patients with Gastric Cancer. J Interferon Cytokine Res. 2019;39(3):155-63.

Abdollahi H, Shams S, Zahedi MJ, Darvish Moghadam S, Hayatbakhsh MM, Jafarzadeh A. IL-10, TNF-alpha and IFN-gamma levels in serum and stomach mucosa of Helicobacter pylori-infected patients. Iran J Allergy Asthma Immunol. 2011;10(4):267-71.

Lindgren A, Yun CH, Sjoling A, Berggren C, Sun JB, Jonsson E, et al. Impaired IFN-gamma production after stimulation with bacterial components by natural killer cells from gastric cancer patients. Exp Cell Res. 2011;317(6):849-58.

Sanchez-Zauco N, Torres J, Gomez A, Camorlinga-Ponce M, Munoz-Perez L, Herrera-Goepfert R, et al. Circulating blood levels of IL-6, IFN-gamma, and IL-10 as potential diagnostic biomarkers in gastric cancer: a controlled study. BMC Cancer. 2017;17(1):384.

Tu SP, Quante M, Bhagat G, Takaishi S, Cui G, Yang XD, et al. IFN-gamma inhibits gastric carcinogenesis by inducing epithelial cell autophagy and T-cell apoptosis. Cancer Res. 2011;71(12):4247-59.

Ito N, Tsujimoto H, Ueno H, Xie Q, Shinomiya N. Helicobacter pylori-Mediated Immunity and Signaling Transduction in Gastric Cancer. J Clin Med. 2020;9(11):3699.

Perfetto B, Buommino E, Canozo N, Paoletti I, Corrado F, Greco R, et al. Interferon-gamma cooperates with Helicobacter pylori to induce iNOS-related apoptosis in AGS gastric adenocarcinoma cells. Res Microbiol. 2004;155(4):259-66.

Szczepanik AM, Scislo L, Scully T, Walewska E, Siedlar M, Kolodziejczyk P, et al. IL-6 serum levels predict postoperative morbidity in gastric cancer patients. Gastric Cancer. 2011;14(3):266-73.

Madej-Michniewicz A, Budkowska M, Salata D, Dolegowska B, Starzynska T, Blogowski W. Evaluation of selected interleukins in patients with different gastric neoplasms: a preliminary report. Sci Rep. 2015;5(1):14382.

Yin Y, Si X, Gao Y, Gao L, Wang J. The nuclear factor-kappaB correlates with increased expression of interleukin-6 and promotes progression of gastric carcinoma. Oncol Rep. 2013;29(1):34-8.

Bockerstett KA, DiPaolo RJ. Regulation of Gastric Carcinogenesis by Inflammatory Cytokines. Cell Mol Gastroenterol Hepatol. 2017;4(1):47-53.

Zhang XY, Zhang PY, Aboul-Soud MA. From inflammation to gastric cancer: Role of Helicobacter pylori. Oncol Lett. 2017;13(2):543-48.

Rija FF, Hussein SZ, Abdalla MA. Physiological and Immunological Disturbance in Rheumatoid Arthritis Patients. Baghdad Sci J. 2021;18(2):0247-47.

Wang Z, Si X, Xu A, Meng X, Gao S, Qi Y, et al. Activation of STAT3 in human gastric cancer cells via interleukin (IL)-6-type cytokine signaling correlates with clinical implications. PLoS One. 2013;8(10):e75788.

Hara M, Nagasaki T, Shiga K, Takahashi H, Takeyama H. High serum levels of interleukin-6 in patients with advanced or metastatic colorectal cancer: the effect on the outcome and the response to chemotherapy plus bevacizumab. Surg Today. 2017;47(4):483-89.

Kruk J, Aboul-Enein HY. Reactive Oxygen and Nitrogen Species in Carcinogenesis: Implications of Oxidative Stress on the Progression and Development of Several Cancer Types. Mini Rev Med Chem. 2017;17(11):904-19.

Aldeen YM, Habeeb P, Jawad AH. Study Oxidative Stress Statues In Hypertension Women. Baghdad Sci J. 2016;13(2):407-13.

Rezatabar S, Karimian A, Rameshknia V, Parsian H, Majidinia M, Kopi TA, et al. RAS/MAPK signaling functions in oxidative stress, DNA damage response and cancer progression. J Cell Physiol. 2019;234(9):14951-65.

Kryston TB, Georgiev AB, Pissis P, Georgakilas AG. Role of oxidative stress and DNA damage in human carcinogenesis. Mutat Res. 2011;711(1-2):193-201.

Leung EY, Crozier JE, Talwar D, O'Reilly DS, McKee RF, Horgan PG, et al. Vitamin antioxidants, lipid peroxidation, tumour stage, the systemic inflammatory response and survival in patients with colorectal cancer. Int J Cancer. 2008;123(10):2460-464.

Fu XL, Duan W, Su CY, Mao FY, Lv YP, Teng YS, et al. Interleukin 6 induces M2 macrophage differentiation by STAT3 activation that correlates with gastric cancer progression. Cancer Immunol Immunother. 2017;66(12):1597-608.

Kabir S, Daar GA. Serum levels of interleukin-1, interleukin-6 and tumour necrosis factor-alpha in patients with gastric carcinoma. Cancer Lett. 1995;95(1-2):207-12.

Guo L, Ou JL, Zhang T, Ma L, Qu LF. Effect of expressions of tumor necrosis factor alpha and interleukin 1B on peritoneal metastasis of gastric cancer. Tumour Biol. 2015;36(11):8853-60.

Al Obeed OA, Alkhayal KA, Al Sheikh A, Zubaidi AM, Vaali-Mohammed MA, Boushey R, et al. Increased expression of tumor necrosis factor-alpha is associated with advanced colorectal cancer stages. World J Gastroenterol. 2014;20(48):18390-6.

Mojic M, Takeda K, Hayakawa Y. The Dark Side of IFN-γ: Its Role in Promoting Cancer Immunoevasion. Int J Mol Sci. 2018;19(1):89.

Tseng PC, Chen CL, Shan YS, Lin CF. An increase in galectin-3 causes cellular unresponsiveness to IFN-gamma-induced signal transduction and growth inhibition in gastric cancer cells. Oncotarget. 2016;7(12):15150-60.

Xu YH, Li ZL, Qiu SF. IFN-gamma Induces Gastric Cancer Cell Proliferation and Metastasis Through Upregulation of Integrin beta3-Mediated NF-kappaB Signaling. Transl Oncol. 2018;11(1):182-92.

Hall C, Clarke L, Pal A, Buchwald P, Eglinton T, Wakeman C, et al. A Review of the Role of Carcinoembryonic Antigen in Clinical Practice. Ann Coloproctol. 2019;35(6):294-305.

التنزيلات

منشور

2022-12-01

إصدار

القسم

article

كيفية الاقتباس

1.
إرتباط محركات الخلية الالتهابية القوية بالمؤشرات الحيوية لتلف الحمض النووي المؤكسد في مرضى سرطان المعدة. Baghdad Sci.J [انترنت]. 1 ديسمبر، 2022 [وثق 17 مايو، 2024];19(6):1313. موجود في: https://bsj.uobaghdad.edu.iq/index.php/BSJ/article/view/6589

المؤلفات المشابهة

يمكنك أيضاً إبدأ بحثاً متقدماً عن المشابهات لهذا المؤلَّف.