NOVÁK, Jan, Jiří ŠÁNA, Tibor STRAČINA, Marie NOVÁKOVÁ and Ondřej SLABÝ. Doxorubicin and Liposomal Doxorubicin Differentially Affect Expression of miR-208a and let-7g in Rat Ventricles and Atria. Cardiovascular Toxicology. Totowa: Humana Press, 2017, vol. 17, No 3, p. 355-359. ISSN 1530-7905. Available from: https://dx.doi.org/10.1007/s12012-016-9393-8.
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Basic information
Original name Doxorubicin and Liposomal Doxorubicin Differentially Affect Expression of miR-208a and let-7g in Rat Ventricles and Atria
Authors NOVÁK, Jan (203 Czech Republic, guarantor, belonging to the institution), Jiří ŠÁNA (203 Czech Republic, belonging to the institution), Tibor STRAČINA (703 Slovakia, belonging to the institution), Marie NOVÁKOVÁ (203 Czech Republic, belonging to the institution) and Ondřej SLABÝ (203 Czech Republic, belonging to the institution).
Edition Cardiovascular Toxicology, Totowa, Humana Press, 2017, 1530-7905.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30201 Cardiac and Cardiovascular systems
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 2.989
RIV identification code RIV/00216224:14110/17:00096001
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1007/s12012-016-9393-8
UT WoS 000404172500014
Keywords in English Cardiotoxicity; Doxorubicin; let-7g; lipodox; microRNAs; miR-208a
Tags EL OK, podil
Tags International impact, Reviewed
Changed by Changed by: Soňa Böhmová, učo 232884. Changed: 21/3/2018 16:35.
Abstract
Anthracyclines use is limited by profound cardiotoxicity. Involvement of miRNAs in anthracycline-induced cardiotoxicity (AIC) is still not completely understood. Thus, the expression of AIC-related microRNAs was determined in rat atria and ventricles after doxorubicin (DOX) and liposomal doxorubicin (L-DOX) administration. Vehiculum, DOX or L-DOX were applied intraperitoneally in a single dose to male Wistar rats (3 groups: control, DOX and L-DOX, respectively). Rats were sacrificed after 24 h, and samples from left atrium (LA)/ventricle (LV) and right atrium (RA)/ventricle (RV) were obtained. Expressions of miR-208a, let-7g and snU6 were determined using qRT-PCR. In the control group, miR-208a was highly abundant in the atria compared to the ventricles and in the left-sided structures compared to the right-sided structures, while let-7g showed only atrio-ventricular gradient with predominant expression in the atria. Administration of both DOX and L-DOX resulted in 38.87 and 23.57% reduction in miR-208a expression in the LV (p = 0.028) and in 13.79 and 14.70% reduction in let-7g expression in the LA (p = 0.015), respectively. Acute administration of DOX/L-DOX alters expression of miR-208a in LV and of let-7g in LA. These changes may partly contribute to the development of AIC.
Links
ED1.1.00/02.0068, research and development projectName: CEITEC - central european institute of technology
MUNI/A/1326/2014, interní kód MUName: Kardiovaskulární systém od buňky k lůžku pacienta (Acronym: KASBUNPAC)
Investor: Masaryk University, Category A
MUNI/A/1365/2015, interní kód MUName: Kardiovaskulární systém: od modelu přes terapii k prevenci (Acronym: KAMOTEPRE)
Investor: Masaryk University, Category A
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