Interrelation between Pseudomonas aeruginosa quinolone signal and the level of immunoglobulins in the blood of patients with lung cancer
- Authors: Shestopalov A.V.1,2, Кit O.I.3, Davydov V.V.1, Baizyanova Y.M.1, Zlatnik E.Y.3, Novikova I.A.3, Sagakyants A.B.3, Appolonova S.A.2, Moskaleva N.E.2, Rumyantsev S.A.1,2
-
Affiliations:
- Pirogov Russian National Research Medical University, Ministry of Health of Russia
- Center of Digital and Translational Biomedicine, Сenter of Molecular Health
- National Medical Research Center of Oncology, Ministry of Health of Russia
- Issue: Vol 10, No 2 (2023)
- Pages: 126-131
- Section: EXPERIMENTAL REPORT
- Published: 10.07.2023
- URL: https://umo.abvpress.ru/jour/article/view/548
- DOI: https://doi.org/10.17650/2313-805X-2023-10-2-126-131
- ID: 548
Cite item
Full Text
Abstract
Introduction. Researchers in the field of oncology have a significant interest in the role of microorganisms in development of malignant neoplasms.
Aim. To study the levels of 2-heptyl-3-hydroxy-4-quinolone (PQS) and 2-heptyl-4-quinolone (HHQ) produced by Pseudomonas aeruginosa in the blood of patients with lung cancer and to analyze the relation between their changes and changes in the level of immunoglobulins and vascular endothelial growth factor (VEGF) in the blood of patients with lung cancer.
Materials and methods. PQS and HHQ were quantified in the blood of patients using high performance liquid chromatography. The levels of immunoglobulins G (IgG), secretory immunoglobulin A (s-IgA), and VEGF in the blood were determined using ELISA.
Results. Analysis have shown that the level of PQS in the blood of patients with lung cancer is 2-fold higher than in the control group. This change is accompanied by a decrease in the level of immunoglobulins IgG, as well as an increase in the content of s-IgA and growth factor VEGF in the blood.
Conclusion. PQS level in the blood of patients with lung cancer is elevated creating conditions aggravating the course of the main disease and worsening its prognosis.
About the authors
A. V. Shestopalov
Pirogov Russian National Research Medical University, Ministry of Health of Russia; Center of Digital and Translational Biomedicine, Сenter of Molecular Health
Email: fake@neicon.ru
ORCID iD: 0000-0002-1428-7706
1 Ostrovityanova St., Moscow 117997; Bld. 1, 32 Nakhimovskii prospekt, Moscow 117218
Russian FederationO. I. Кit
National Medical Research Center of Oncology, Ministry of Health of Russia
Email: fake@neicon.ru
ORCID iD: 0000-0003-3061-6108
14th Line, Rostov-on-Don 344037
Russian FederationV. V. Davydov
Pirogov Russian National Research Medical University, Ministry of Health of Russia
Author for correspondence.
Email: vaddavydov@mail.ru
ORCID iD: 0000-0002-3347-1832
Vadim V. Davydov.
1 Ostrovityanova St., Moscow 117997
Russian FederationYa. M. Baizyanova
Pirogov Russian National Research Medical University, Ministry of Health of Russia
Email: fake@neicon.ru
1 Ostrovityanova St., Moscow 117997
Russian FederationE. Yu. Zlatnik
National Medical Research Center of Oncology, Ministry of Health of Russia
Email: fake@neicon.ru
ORCID iD: 0000-0002-1410-122X
14th Line, Rostov-on-Don 344037
Russian FederationI. A. Novikova
National Medical Research Center of Oncology, Ministry of Health of Russia
Email: fake@neicon.ru
ORCID iD: 0000-0002-6496-9641
14th Line, Rostov-on-Don 344037
Russian FederationA. B. Sagakyants
National Medical Research Center of Oncology, Ministry of Health of Russia
Email: fake@neicon.ru
ORCID iD: 0000-0003-0874-5261
14th Line, Rostov-on-Don 344037
Russian FederationS. A. Appolonova
Center of Digital and Translational Biomedicine, Сenter of Molecular Health
Email: fake@neicon.ru
ORCID iD: 0000-0002-9032-1558
Bld. 1, 32 Nakhimovskii prospekt, Moscow 117218
Russian FederationN. E. Moskaleva
Center of Digital and Translational Biomedicine, Сenter of Molecular Health
Email: fake@neicon.ru
ORCID iD: 0000-0002-7309-8913
Bld. 1, 32 Nakhimovskii prospekt, Moscow 117218
Russian FederationS. A. Rumyantsev
Pirogov Russian National Research Medical University, Ministry of Health of Russia; Center of Digital and Translational Biomedicine, Сenter of Molecular Health
Email: fake@neicon.ru
1 Ostrovityanova St., Moscow 117997; Bld. 1, 32 Nakhimovskii prospekt, Moscow 117218
Russian FederationReferences
- Bagirov N.S., Petukhov I.N., Dmitriev N.V., Grigorevskaia Z.V. Microbiom and cancer: is there interconnection? Literature review. Zlokachestvennye opukholi = Malignant tumors 2018;3(1):56–69. (In Russ.). doi: 10.18027/2224-5057-2018-8-3s1-56-69
- Aadra P.B., Matthew R.R., Scott J.B. The role of the microbiome in cancer development and therapy. CA Cancer J Clin 2017;67(4):326–44. doi: 10.3322/caac.21398
- Sánchez-Alcoholado L., Ramos-Molina B., Otero A. et al. The Role of the gut microbiome in colorectal cancer development and therapy response. Cancers 2020;12(6):1406. doi: 10.3390/cancers12061406
- Teles F.R.F., Alawi F., Castilho R.M., Wang Y. Association or causation? Exploring the oral microbiome and cancer links. J Dent Res 2020;99:1411–24. doi: 10.1177/0022034520945242
- Maurice N.M., Bedi B., Sadikot R.T. Pseudomonas aeruginosa biofilms: host response and clinical implications in lung infections. Am J Respir Cell Mol Biol 2018;58(4):428–39. doi: 10.1165/rcmb.2017-0321TR
- Riquelme S.A., Liimatta K., Fok Lung T.W. et al. Pseudomonas aeruginosa utilizes host-derived itaconate to redirect its metabolism to promote biofilm formation. Cell Metab 2020;31(6):1091–106. doi: 10.1016/j.cmet.2020.04.017
- Garcia-Nuñez M., Marti S., Puig C. et al. Bronchial microbiome, PA biofilm-forming capacity and exacerbation in severe COPD patients colonized by P. aeruginosa. Future Microbiol 2017;12: 379–92. doi: 10.2217/fmb-2016-0127
- Biswas A., Mehta H.J., Folch E.E. Chronic obstructive pulmonary disease and lung cancer: inter-relationships. Curr Opin Pulm Med 2018;24(2):152–60. doi: 10.1097/MCP.0000000000000451
- Patel B., Priefer R. Impact of chronic obstructive pulmonary disease, lung infection, and/or inhaled corticosteroids use on potential risk of lung cancer. Life Sci 2022;294:120374. doi: 10.1016/j.lfs.2022.120374
- Montagut E.J., Marco M.P. Biological and clinical significance of quorum sensing alkylquinolones: current analytical and bioanalytical methods for their quantification. Anal Bioanal Chem 2021;413(18):4599–618. doi: 10.1007/s00216-021-03356-x
- Yang L., Yuan T.J., Wan Y. et al. Quorum sensing: a new perspective to reveal the interaction between gut microbiota and host. Future Microbiol 2022;17:293–309. doi: 10.2217/fmb-2021-0217
- Liu Y.-C., Hussain F., Negm O. et al. Contribution of the alkylquinolone quorum-sensing system to the interaction of Pseudomonas aeruginosa with bronchial epithelial cells. Front Microbiol 2018;9–11. doi: 10.3389/fmicb.2018.03018
- Azam M.W., Khan A.U. Updates on the pathogenicity status of Pseudomonas aeruginosa. Drug Discov Today 2019;24(1):350–9. doi: 10.1016/j.drudis.2018.07.003
- Warrier A., Satyamoorthy K., Murali T.S. Quorum-sensing regulation of virulence factors in bacterial biofilm. Future Microbiol 2021;16:1003–21. doi: 10.2217/fmb-2020-0301
- Liu C.Y., Xie W.G., Tian J.W., Li J. A comparatively study on inflammatory factors and immune functions of lung cancer and pulmonary ground glass attenuation. Eur Rev Med Pharmacol Sci 2017;21(18):4098–103.
- Abolfathi H., Sheikhpour M., Shahraeini S.S. et al. Studies in lung cancer cytokine proteomics: a review. Expert Rev Proteomics 2021;18(1):49–64. doi: 10.1080/14789450.2021.1892491
- Rampioni G., Falcone M., Heeb S. et al. Unravelling the genome-wide contributions of specific 2-alkyl-4-quinolones and PqsE to quorum sensing in Pseudomonas aeruginosa. PLoS Pathog 2016;12(11):e1006029. doi: 10.1371/journal.ppat.1006029
- Kim K., Kim Y.U., Koh B.H. et al. HHQ and PQS, two Pseudomonas aeruginosa quorum-sensing molecules, down-regulate the innate immune responses through the nuclear factor-kappaB pathway. Immunology 2010;129:578–88. doi: 10.1111/j.1365-2567.2009.03160.x
- Hansch G.M., Prior B., Brenner-Weiss G. et al. The Pseudomonas quinolone signal (PQS) stimulates chemotaxis of polymorphonuclear neutrophils. Appl Biomater Funct Mater 2014;12:21–6. doi: 10.5301/jabfm.5000204
- Lin J., Cheng J., Wang Y., Shen X. The pseudomonas quinolone signal (PQS): not just for quorum sensing anymore. Front Cell Infect Microbiol 2018;8:230. doi: 10.3389/fcimb.2018.00230
- Jing Y., Chen X., Li K. et al. Association of antibiotic treatment with immune-related adverse events in patients with cancer receiving immunotherapy. J Immunother Cancer 2022;10(1):e003779. doi: 10.1136/jitc-2021-003779
Supplementary files


