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Search of MicroRNAs Regulating the Receptor Status of Breast Cancer In Silico and Experimental Confirmation of Their Expression in Tumors. / Chernyi, V. S.; Tarasova, P. V.; Kozlov, V. V. et al.

In: Bulletin of Experimental Biology and Medicine, Vol. 163, No. 5, 01.09.2017, p. 655-659.

Research output: Contribution to journal › Article › peer-review

Harvard

Chernyi, VS, Tarasova, PV, Kozlov, VV, Saik, OV, Kushlinskii, NE & Gulyaeva, LF 2017, 'Search of MicroRNAs Regulating the Receptor Status of Breast Cancer In Silico and Experimental Confirmation of Their Expression in Tumors', Bulletin of Experimental Biology and Medicine, vol. 163, no. 5, pp. 655-659. https://doi.org/10.1007/s10517-017-3872-1

APA

Chernyi, V. S., Tarasova, P. V., Kozlov, V. V., Saik, O. V., Kushlinskii, N. E., & Gulyaeva, L. F. (2017). Search of MicroRNAs Regulating the Receptor Status of Breast Cancer In Silico and Experimental Confirmation of Their Expression in Tumors. Bulletin of Experimental Biology and Medicine, 163(5), 655-659. https://doi.org/10.1007/s10517-017-3872-1

Vancouver

Chernyi VS, Tarasova PV, Kozlov VV, Saik OV, Kushlinskii NE, Gulyaeva LF. Search of MicroRNAs Regulating the Receptor Status of Breast Cancer In Silico and Experimental Confirmation of Their Expression in Tumors. Bulletin of Experimental Biology and Medicine. 2017 Sept 1;163(5):655-659. doi: 10.1007/s10517-017-3872-1

Author

Chernyi, V. S. ; Tarasova, P. V. ; Kozlov, V. V. et al. / Search of MicroRNAs Regulating the Receptor Status of Breast Cancer In Silico and Experimental Confirmation of Their Expression in Tumors. In: Bulletin of Experimental Biology and Medicine. 2017 ; Vol. 163, No. 5. pp. 655-659.

BibTeX

@article{5e27057a42a54ce5b9cb5536cd31ba59,
title = "Search of MicroRNAs Regulating the Receptor Status of Breast Cancer In Silico and Experimental Confirmation of Their Expression in Tumors",
abstract = "MicroRNA whose expression depends on the receptor status of breast cancer were selected using bioinformatic analysis. The expression of 9 microRNAs (16, 17, 21, 27, 125, 146, 155, 200a, and 221) was analyzed in 76 samples of breast cancer with various receptor phenotypes. The expression of microRNAs 155, 27, and 200a did not differ in various types of breast cancer. The data on positive correlation between the expression of microRNA-21 and microRNA-221 and negative receptor status of the tumor were confirmed. The expression of the tumor suppressing microRNA-125b decreased in samples of breast cancer expressing HER2 and ER and in triple negative breast cancer, which characterizes it as a universal marker of breast cancer. An increase in the expression of microRNA-16 was shown in samples of breast cancer expressing HER2 and ER. The expression of microRNA-17 decreased in triple negative breast cancer and increased in ER+, PR+, and HER+ types of breast cancer. MicroRNAs 16, 17, 21, 125b, 146b, and 221 can be promising markers for differential diagnostics of various phenotypes of breast cancer.",
keywords = "breast cancer, HER2, in silico, microRNA, receptors of estrogen and progesterone",
author = "Chernyi, {V. S.} and Tarasova, {P. V.} and Kozlov, {V. V.} and Saik, {O. V.} and Kushlinskii, {N. E.} and Gulyaeva, {L. F.}",
year = "2017",
month = sep,
day = "1",
doi = "10.1007/s10517-017-3872-1",
language = "English",
volume = "163",
pages = "655--659",
journal = "Bulletin of Experimental Biology and Medicine",
issn = "0007-4888",
publisher = "Springer New York",
number = "5",

}

RIS

TY - JOUR

T1 - Search of MicroRNAs Regulating the Receptor Status of Breast Cancer In Silico and Experimental Confirmation of Their Expression in Tumors

AU - Chernyi, V. S.

AU - Tarasova, P. V.

AU - Kozlov, V. V.

AU - Saik, O. V.

AU - Kushlinskii, N. E.

AU - Gulyaeva, L. F.

PY - 2017/9/1

Y1 - 2017/9/1

N2 - MicroRNA whose expression depends on the receptor status of breast cancer were selected using bioinformatic analysis. The expression of 9 microRNAs (16, 17, 21, 27, 125, 146, 155, 200a, and 221) was analyzed in 76 samples of breast cancer with various receptor phenotypes. The expression of microRNAs 155, 27, and 200a did not differ in various types of breast cancer. The data on positive correlation between the expression of microRNA-21 and microRNA-221 and negative receptor status of the tumor were confirmed. The expression of the tumor suppressing microRNA-125b decreased in samples of breast cancer expressing HER2 and ER and in triple negative breast cancer, which characterizes it as a universal marker of breast cancer. An increase in the expression of microRNA-16 was shown in samples of breast cancer expressing HER2 and ER. The expression of microRNA-17 decreased in triple negative breast cancer and increased in ER+, PR+, and HER+ types of breast cancer. MicroRNAs 16, 17, 21, 125b, 146b, and 221 can be promising markers for differential diagnostics of various phenotypes of breast cancer.

AB - MicroRNA whose expression depends on the receptor status of breast cancer were selected using bioinformatic analysis. The expression of 9 microRNAs (16, 17, 21, 27, 125, 146, 155, 200a, and 221) was analyzed in 76 samples of breast cancer with various receptor phenotypes. The expression of microRNAs 155, 27, and 200a did not differ in various types of breast cancer. The data on positive correlation between the expression of microRNA-21 and microRNA-221 and negative receptor status of the tumor were confirmed. The expression of the tumor suppressing microRNA-125b decreased in samples of breast cancer expressing HER2 and ER and in triple negative breast cancer, which characterizes it as a universal marker of breast cancer. An increase in the expression of microRNA-16 was shown in samples of breast cancer expressing HER2 and ER. The expression of microRNA-17 decreased in triple negative breast cancer and increased in ER+, PR+, and HER+ types of breast cancer. MicroRNAs 16, 17, 21, 125b, 146b, and 221 can be promising markers for differential diagnostics of various phenotypes of breast cancer.

KW - breast cancer

KW - HER2

KW - in silico

KW - microRNA

KW - receptors of estrogen and progesterone

UR - http://www.scopus.com/inward/record.url?scp=85029909471&partnerID=8YFLogxK

U2 - 10.1007/s10517-017-3872-1

DO - 10.1007/s10517-017-3872-1

M3 - Article

AN - SCOPUS:85029909471

VL - 163

SP - 655

EP - 659

JO - Bulletin of Experimental Biology and Medicine

JF - Bulletin of Experimental Biology and Medicine

SN - 0007-4888

IS - 5

ER -

ID: 9906039