Expression of Receptor Tyrosine Kinases on Peripheral Blood Lymphocyte Subpopulations in Patients with Renal Cell Carcinoma and Healthy Volunteers
https://doi.org/10.18027/2224-5057-2019-9-4-18-24
Abstract
Introduction: tyrosine kinases receptors (RTKs) play an important role in the pathogenesis of renal cell carcinoma (RCC). RTKs were studied on tumor and endothelial cells, but the presence of these receptors on lymphocytes was not confirmed. The objective of this study was to investigate the expression of tyrosine kinases receptors on lymphocyte subpopulations in healthy volunteers and RCC patients before and after removal of the primary tumor.
Materials and methods: the study included 19 patients with pT1‑T3N0 / N+M0 / M+ RCC, subjected to nephrectomy, and 10 healthy volunteers. Blood samples were collected once from healthy donors and twice from RCC patients, immediately before and 180 days after surgery. Isolation of lymphocytes and flow cytometry were carried out using standard methods. A comparative analysis of RTKs expression levels in peripheral lymphocytes from healthy volunteers and RCC patients, as well as in RCC patients before and after the operation, was carried out. A search was performed for correlations between the initial RTKs expression on lymphocytes from RCC patients and characteristics of the tumor development, as well as the disease prognosis.
Results: VEGFR-1, -2, -3, FGFR2, PDGFRα, β RTKs are expressed on CD45+ peripheral blood mononuclear cells, as well as subpopulations of CD3+ and CD8+ lymphocytes in healthy volunteers and untreated patients with RCC. No differences in the expression levels of all studied RTKs between subpopulations of lymphocytes were found in RCC patients (p > 0.05 for all). The level of RTKs expression on CD45+ peripheral cells in RCC patients before treatment is significantly lower than in healthy volunteers (p < 0.05 for all). The degree of a decrease in RTKs expression correlated with the pT status and the presence of tumor-associated venous thrombosis. A significant increase in the expression levels of VEGFR1 (on CB45+) and VEGFR2 (on CD8+, CD3+) (p < 0.05 for all) was noted 180 days after the removal of the primary tumor in patients with RCC. No other significant changes in RTKs production were identified. We were not able to determine the effect of RTKs expression on the RCC outcome.
Conclusions: lymphocytes express RTKs, their expression is more pronounced in healthy people than in patients with RCC. After surgical treatment, the RTKs expression becomes restored.
About the Authors
M. I. VolkovaRussian Federation
MD, PhD, DSc, leading research associate, Dept. of Oncourology
Moscow
A. S. Olshanskaya
Russian Federation
oncologist, Department of Organization and Conduct of Clinical Trials
Moscow
D. A. Khochenkov
Russian Federation
MD, PhD. Biol, Head of the Laboratory of Biomarkers and Mechanisms of Tumor Angiogenesis, Research Institute for Experimental Diagnosis and Treatment of Tumors; Professor, Center for Medical Chemistry, Institute of Chemistry and Energy
Moscow
Togliatti
S. A. Ashuba
Russian Federation
Research Assistant, Laboratory of Biomarkers and Mechanisms of Tumor Angiogenesis, Research Institute for Experimental Diagnosis and Treatment of Tumors
Moscow
Yu. A. Khochenkova
Russian Federation
Junior Researcher, Laboratory of Biomarkers and Tumor Angiogenesis Mechanisms, Research Institute for Experimental Diagnosis and Treatment of Tumors
Moscow
I. V. Tsimafeyeu
Russian Federation
Moscow
References
1. Tsimafeyeu I, Zolotareva T, Varlamov S, et al. Five‑year Survival of Patients With Metastatic Renal Cell Carcinoma in the Russian Federation: Results From the RENSUR5 Registry. Clin Genitourin Cancer. 2017 Dec;15 (6):e1069‑e1072.
2. Cancer Genome Atlas Research Network. Comprehensive molecular characterization of clear cell renal cell carcinoma. Nature. 2013;499 (7456):43 – 9.
3. Schodel J, Grampp S, Maher ER, et al. Hypoxia, hypoxia‑inducible transcription factors, and renal cancer. Eur Urol. 2016;69 (4):646 – 57.
4. Tsimafeyeu I, Bratslavsky G. Fibroblast growth factor pathway in renal cell carcinoma. Oncology. 2015;88 (6):321 – 31.
5. Tsimafeyeu I, Ludes‑Meyers J, Stepanova E, et al. Targeting FGFR2 with alofanib (RPT835) shows potent activity in tumour models. Eur J Cancer. 2016 Jul;61:20 – 8.
6. Matveev V. В., Olshanskaya A. S., Volkova M. I. Cabozantinib: from studies to clinical practice. Cancer Urology. 2019;15 (3):28 – 41. (In Russ.).
7. Figlin R. A., Hutson T. E., Tomczac P. et al. Overall survival with sunitinib versus interferon alfa as first‑line treatment in metastatic renal‑cell carcinoma. ASCO Annual Meeting Proceedings 2008. J Clin Oncol 2008;26 (Suppl.): 5024.
8. Matveev VB, Volkova MI. Re: Cytoreductive Nephrectomy for Renal Cell Carcinoma with Venous Tumor Thrombus. Eur Urol. 2017 Dec;72 (6):1024. doi: 10.1016 / j. eururo. 2017.08.029.
9. Rini B. I., Escudier B. J., Michaelson M. D. et al. Phase III AXIS trial for second‑line metastatic renal cell carcinoma (mRCC): Effect of prior first‑line treatment duration and axitinib dose titration on axitinib efficacy. J ClinOncol 2012;30 (Suppl. 5):354.
10. Khochenkov D, Volkova M, Olshanskaia A, et al., 59P Is there receptor tyrosine kinases expression on lymphocytes in patients with renal cell carcinoma? First‑in‑human study. Annals of Oncology, Volume 28, Issue suppl_5, September 2017, mdx361.054, https://doi.org / 10.1093 / annonc / mdx361.054
11. Kopecký O, Lukesová S, Vroblová V, Phenotype analysis of tumour‑infiltrating lymphocytes and lymphocytes in peripheral blood in patients with renal carcinoma. ActaMedica (Hradec Kralove). 2007;50 (3):207 – 12.
12. Kowalczyk D, Skorupski W, Kwias Z, Nowak J. Flow cytometric analysis of tumour‑infiltrating lymphocytes in patients with renal cell carcinoma. Br J Urol. 1997 Oct;80 (4):543 – 7.
13. Fujimoto K, Ichimori Y, Yamaguchi H, et al. Basic fibroblast growth factor as a candidate tumor marker for renal cell carcinoma. Jpn J Cancer Res 86:182 – 186.
14. Khochenkov DA, Solomko ES, Peretolchina NM, et al. Antiangiogenic Activity of Alofanib, an Allosteric Inhibitor of Fibroblast Growth Factor Receptor 2. Bull Exp Biol Med. 2015 Nov;160 (1):84 – 7.
Review
For citations:
Volkova M.I., Olshanskaya A.S., Khochenkov D.A., Ashuba S.A., Khochenkova Yu.A., Tsimafeyeu I.V. Expression of Receptor Tyrosine Kinases on Peripheral Blood Lymphocyte Subpopulations in Patients with Renal Cell Carcinoma and Healthy Volunteers. Malignant tumours. 2019;9(4):18-24. (In Russ.) https://doi.org/10.18027/2224-5057-2019-9-4-18-24