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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Doxorubicin modulated clock genes and cytokines in macrophages extracted from tumor-bearing mice

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Author(s):
Teixeira, Alexandre Abilio S. [1] ; Biondo, Luana Amorim [1] ; Silveira, Loreana S. [1] ; Lima, Edson A. [1] ; Batatinha, Helena A. [1] ; Diniz, Tiego A. [1] ; De Souza, Camila Oliveira [1] ; Comin, Jeferson [1] ; Rosa Neto, Jose Cesar [1]
Total Authors: 9
Affiliation:
[1] Univ Sao Paulo, Inst Biomed Sci, Sao Paulo - Brazil
Total Affiliations: 1
Document type: Journal article
Source: CANCER BIOLOGY & THERAPY; JAN 2020.
Web of Science Citations: 0
Abstract

Circadian rhythm is essential for cellular regulation of physiological, metabolic, and immune functions. Perturbations of circadian rhythms have been correlated with increased susceptibility to cancer and poor prognosis in the cancer treatment. Our aim is to investigate the role of doxorubicin (DOX) treatment on clock genes expression and inflammation in intraperitoneal macrophages and the antitumoral response. Methods: Macrophages were extracted from intraperitoneal cavity of mice without or with Lewis lung carcinoma (LLC) and treated with DOX totaling four groups (CTL, LLC, LLC+DOX and DOX) and analyzes of clock genes in six time points (ZT02, ZT06, ZT10, ZT14, ZT18 AND ZT22). Intraperitoneal macrophages cell culture was stimulated with LPS and DOX and clock genes and inflammatory profile were analyzed. In tumor were analyzed macrophages markers. Results: The expression of F4/80 (ZT22) and CD11c (ZT06) tumor tissue was significantly differed between LLC and LCC+DOX groups. In the intraperitoneal macrophages, DOX increased Clock (ZT10), Rev-Erb alpha (ZT18 and ZT22) and Per2 expressions (ZT18); in the LLC+DOX group was increased Bmal1 (ZT10), Per2 (ZT18) and NF-kB (ZT22) expressions; IL-6 expression increased in the LCC group (ZT02). In intraperitoneal macrophages cell culture stimulated with DOX and LPS after 24 h decreased Clock and Per1. DOX causes depression after 6 and 24 h in TNF-alpha content and Per2 gene expression after 24 h IL-1 beta expression was reduced also. Conclusion: DOX treatment in vivo disrupted cytokine and clock genes expression in intraperitoneal macrophages suppressing immune response. Moreover, macrophages cultured with DOX had decreased expression of LPS-stimulated inflammatory cytokines. (AU)

FAPESP's process: 15/16777-0 - Physical exercise as a synchronizer of circadian rhythms in cancer
Grantee:Alexandre Abilio de Souza Teixeira
Support type: Scholarships in Brazil - Doctorate
FAPESP's process: 19/09854-9 - Effect of doxorubicin upon the adipose tissue: elucidation the role of PPARs family
Grantee:José Cesar Rosa Neto
Support type: Regular Research Grants
FAPESP's process: 16/01409-8 - The caracterization of antiinflammatory effect of palmitoleic acid suplemmentation in hepatic inflammation; The role of PPARs.
Grantee:José Cesar Rosa Neto
Support type: Regular Research Grants