Research output: Contribution to journal › Article › peer-review
Proteome analysis of circulating exosomes in health and breast cancer. / Tamkovich, S. N.; Bakakina, Y. S.; Tutanov, O. S. et al.
In: Russian Journal of Bioorganic Chemistry, Vol. 43, No. 2, 01.03.2017, p. 126-134.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Proteome analysis of circulating exosomes in health and breast cancer
AU - Tamkovich, S. N.
AU - Bakakina, Y. S.
AU - Tutanov, O. S.
AU - Somov, A. K.
AU - Kirushina, N. A.
AU - Dubovskaya, L. V.
AU - Volotovski, I. D.
AU - Laktionov, P. P.
PY - 2017/3/1
Y1 - 2017/3/1
N2 - Microvesicles were isolated from blood plasma and total blood of healthy females and breast cancer patients by filtration and ultracentrifugation. According to flow cytometry, different subpopulations of exosomes were represented in blood of healthy donors and cancer patients at different levels with median fluorescence intensity (MFI) values in both groups arranged in the following order: CD24/СD9 > СD9/СD81 > CD9/CD63 = CD24/CD63. Concentration of exosomes in blood plasma of healthy females estimated by nanoparticle tracking analysis (NTA) did not exceed (3.71 ± 1.15) × 107 particles/mL of blood and did not differ from that in plasma of breast cancer patients, which averaged (3.99 ± 1.03) × 107 particles/mL of blood. Concentration of total exosomes in blood (including exosomes from plasma and blood cell surface-bound exosomes) did not depend on the presence/absence of a tumor; the values were (7.66 ± 0.7) × 107 particles/mL of healthy blood and (9.4 ± 1.24) × 107 particles/mL of blood from cancer patients. Comparative analysis of exosomes using 2-D electrophoresis with subsequent analysis of 2-D proteomic maps revealed proteins missing in blood or differentially expressed in healthy females and breast cancer women. The data presented provide the possibility for identification of exosomal proteomic markers and isolation of tumor-specific exosomes, which contributes to the development of breast cancer diagnostics.
AB - Microvesicles were isolated from blood plasma and total blood of healthy females and breast cancer patients by filtration and ultracentrifugation. According to flow cytometry, different subpopulations of exosomes were represented in blood of healthy donors and cancer patients at different levels with median fluorescence intensity (MFI) values in both groups arranged in the following order: CD24/СD9 > СD9/СD81 > CD9/CD63 = CD24/CD63. Concentration of exosomes in blood plasma of healthy females estimated by nanoparticle tracking analysis (NTA) did not exceed (3.71 ± 1.15) × 107 particles/mL of blood and did not differ from that in plasma of breast cancer patients, which averaged (3.99 ± 1.03) × 107 particles/mL of blood. Concentration of total exosomes in blood (including exosomes from plasma and blood cell surface-bound exosomes) did not depend on the presence/absence of a tumor; the values were (7.66 ± 0.7) × 107 particles/mL of healthy blood and (9.4 ± 1.24) × 107 particles/mL of blood from cancer patients. Comparative analysis of exosomes using 2-D electrophoresis with subsequent analysis of 2-D proteomic maps revealed proteins missing in blood or differentially expressed in healthy females and breast cancer women. The data presented provide the possibility for identification of exosomal proteomic markers and isolation of tumor-specific exosomes, which contributes to the development of breast cancer diagnostics.
KW - biomarkers
KW - blood
KW - breast cancer
KW - exosomes
KW - flow cytometry
KW - proteins
KW - proteomics
KW - two-dimensional gel electrophoresis
KW - DIAGNOSIS
KW - RNA
KW - BIOMARKER
KW - MICROVESICLES
KW - HUMAN SALIVA
KW - PLASMA
KW - EXTRACELLULAR VESICLES
KW - PROTEINS
UR - http://www.scopus.com/inward/record.url?scp=85017603248&partnerID=8YFLogxK
U2 - 10.1134/S1068162017020157
DO - 10.1134/S1068162017020157
M3 - Article
AN - SCOPUS:85017603248
VL - 43
SP - 126
EP - 134
JO - Russian Journal of Bioorganic Chemistry
JF - Russian Journal of Bioorganic Chemistry
SN - 1068-1620
IS - 2
ER -
ID: 10263980