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EXPRESSION of MACROPHAGe-ASSOCIATED GENES IN BREAST TUMORS: RELATION TO TUMOR PROGRESSION

https://doi.org/10.21294/1814-4861-2017-16-6-47-56

Abstract

Background. Tumor-associated macrophages (TAM) are the main innate immunity cells that regulate the relationship between the infiltrating immunocompetent cells, tumor cells and other components of the microenvironment. TAMs can promote tumor cell proliferation and angiogenesis and can also contribute to tumor response to chemotherapy. The purpose of the study was to assess the prognostic significance of YKL39 and CCL18 gene expression in breast TAMs prior to treatment. Material and methods. A total of 96 patients with histologically verified invasive breast carcinoma of no special type (T1–4N0–3M0) were included into the study. The patients received 2–4 cycles of neoadjuvant chemotherapy. The 5-year metastasis-free survival was analyzed. The YKL39 and CCL18 expression levels were assessed using TaqMan real-time RTPCR. The expression level of >1 (higher than that in the normal tissue) indicated the gene overexpression. Results. There was no association between the YKL39 and CCL18 gene expression levels and the clinical and pathologic features. However, the levels of YKL39 and CCL18 gene expressions were significantly higher in patients having no distant metastases within a 5-year follow-up. Metastasis-free survival was estimated in patients with overexpression of YKL39 and CCL18 genes (YKL39+CCL18+ ) and in patients with low and high expression levels (YKL39 CCL18 , YKL39 CCL18+, YKL39+CCL18 ) using the Kaplan-Meier method. All 100 % of patients (10 out of 10) with YKL39+CCL18+ macrophage phenotype in a tumor were alive and had no evidence of tumor progression during 5 years of follow-up. In patients with YKL39+CCL18 phenotype, the metastasis-free survival rate was 85 %. In patients with YKL39 CCL18+ and YKL39 CCL18 phenotypes, the 5-year survival rates were 71 % and 69 %, respectively. A statistically significant difference in metastasis-free survival between patients with YKL39+CCL18+ phenotype and YKL39 CCL18+ or YKL39 CCL18 phenotypes was found. Data obtained showed the association between TAM marker gene expression and metastasis free survival of breast cancer patients treated with NACT.

 

About the Authors

N. V. Litviakov
Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Science, Tomsk; National Research Tomsk State University, Tomsk
Russian Federation

PhD

SPIN-code: 2546-0181

AuthorID: 183820



M. M. Tsyganov
Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Science, Tomsk
Russian Federation

PhD

SPIN-code: 1253-0240

AuthorID: 730156



M. K. Ibragimova
Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Science, Tomsk; National Research Tomsk State University, Tomsk
Russian Federation

SPIN-code: 2340-1628

AuthorID: 637822

ResearchID: C-8609-2012

SCOPUS: 57130579200



I. V. Deryusheva
Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Science, Tomsk
Russian Federation

SPIN-code: 5560-6131

AuthorID: 881749



P. V. Kazantseva
Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Science, Tomsk
Russian Federation

MD, PhD

SPIN-code: 7881-6259

AuthorID: 857960



I. V. Mitrofanova
Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Science, Tomsk; National Research Tomsk State University, Tomsk
Russian Federation

MD

SPIN-code: 6272-8422

AuthorID: 56862097400



I. G. Frolova
Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Science, Tomsk
Russian Federation

MD, DSc, Professor

SPIN-code: 9800-9777

AuthorID: 463121

SCOPUS: 7006413170



M. A. Buldakov
Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Science, Tomsk; National Research Tomsk State University, Tomsk
Russian Federation

PhD

SPIN-code: 7558-4726

AuthorID: 7922-2012



E. M. Slonimskaya
Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Science, Tomsk
Russian Federation

MD, DSc, Professor

SPIN-code: 7763-6417

AuthorID: 183823



E. L. Choinzonov
Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Science, Tomsk
Russian Federation

MD, DSc, Professor

SPIN-code: 2240-8730

AuthorID: 550195



Yu. G. Kzhyshkovska
National Research Tomsk State University, Tomsk; Institute of Transfusion Medicine and Immunology, Medical Faculty, Mannheim, University of Heidelberg, Mannheim
Russian Federation
Professor, Tomsk State University (Tomsk, Russia); Institute of Transfusion Medicine and Immunology, Medical Faculty, Mannheim, University of Heidelberg (Mannheim, Germany)


N. V. Cherdyntseva
Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Science, Tomsk; National Research Tomsk State University, Tomsk
Russian Federation

PhD, Professor

SPIN-code: 5344-0990

AuthorID: 81344



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For citations:


Litviakov N.V., Tsyganov M.M., Ibragimova M.K., Deryusheva I.V., Kazantseva P.V., Mitrofanova I.V., Frolova I.G., Buldakov M.A., Slonimskaya E.M., Choinzonov E.L., Kzhyshkovska Yu.G., Cherdyntseva N.V. EXPRESSION of MACROPHAGe-ASSOCIATED GENES IN BREAST TUMORS: RELATION TO TUMOR PROGRESSION. Siberian journal of oncology. 2017;16(6):47-56. (In Russ.) https://doi.org/10.21294/1814-4861-2017-16-6-47-56

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ISSN 1814-4861 (Print)
ISSN 2312-3168 (Online)