Melatonin Regulates the Daily Levels of Plasma Amino Acids, Acylcarnitines, Biogenic Amines, Sphingomyelins, and Hexoses in a Xenograft Model of Triple Negative Breast Cancer
Carregando...
Citações na Scopus
5
Tipo de produção
article
Data de publicação
2022
Título da Revista
ISSN da Revista
Título do Volume
Editora
MDPI
Autores
JUNIOR, Rubens Paula
CHUFFA, Luiz Gustavo de Almeida
SIMAO, Vinicius Augusto
SONEHARA, Nathalia Martins
REITER, Russel J.
ZUCCARI, Debora Aparecida Pires de Campos
Citação
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.23, n.16, article ID 9105, 19p, 2022
Resumo
Metabolic dysregulation as a reflection of specific metabolite production and its utilization is a common feature of many human neoplasms. Melatonin, an indoleamine that is highly available during darkness, has a variety of metabolic functions in solid tumors. Because plasma metabolites undergo circadian changes, we investigated the role of melatonin on the profile of amino acids (AAs), biogenic amines, carnitines, sphingolipids, and hexoses present in the plasma of mice bearing xenograft triple negative breast cancer (MDA-MB-231 cells) over 24 h. Plasma concentrations of nine AAs were reduced by melatonin, especially during the light phase, with a profile closer to that of non-breast cancer (BC) animals. With respect to acylcarnitine levels, melatonin reduced 12 out of 24 molecules in BC-bearing animals compared to their controls, especially at 06:00 h and 15:00 h. Importantly, melatonin reduced the concentrations of asymmetric dimethylarginine, carnosine, histamine, kynurenine, methionine sulfoxide, putrescine, spermidine, spermine, and symmetric dimethylarginine, which are associated with the BC metabolite sets. Melatonin also led to reduced levels of sphingomyelins and hexoses, which showed distinct daily variations over 24 h. These results highlight the role of melatonin in controlling the levels of plasma metabolites in human BC xenografts, which may impact cancer bioenergetics, in addition to emphasizing the need for a more accurate examination of its metabolomic changes at different time points.
Palavras-chave
breast cancer, melatonin, metabolomics, xenografted mice, plasma metabolites, circadian profile
Referências
- Agostinelli E, 2007, AMINO ACIDS, V33, P175, DOI 10.1007/s00726-007-0510-7
- Ahabrach H, 2021, ENDOCR METAB IMMUNE, V21, P1869, DOI 10.2174/1871530320666201201110807
- Anderson G, 2019, BIOCHEM PHARMACOL, V168, P259, DOI 10.1016/j.bcp.2019.07.014
- Beger RD, 2013, METABOLITES, V3, P552, DOI 10.3390/metabo3030552
- Blask DE, 2014, PLOS ONE, V9, DOI 10.1371/journal.pone.0102776
- Blask DE, 2005, CANCER RES, V65, P11174, DOI 10.1158/0008-5472.CAN-05-1945
- Borin TF, 2016, J PINEAL RES, V60, P3, DOI 10.1111/jpi.12270
- Chuffa LGD, 2020, J PINEAL RES, V69, DOI 10.1111/jpi.12693
- Cipolla-Neto J, 2018, ENDOCR REV, V39, P990, DOI 10.1210/er.2018-00084
- Colombo C, 1999, PSYCHIAT RES, V86, P267, DOI 10.1016/S0165-1781(99)00036-0
- Colombo J, 2021, CANCERS, V13, DOI 10.3390/cancers13205233
- Cui L, 2021, J PINEAL RES, V71, DOI 10.1111/jpi.12767
- Currie E, 2013, CELL METAB, V18, P153, DOI 10.1016/j.cmet.2013.05.017
- Dallmann R, 2012, P NATL ACAD SCI USA, V109, P2625, DOI 10.1073/pnas.1114410109
- Chuffa LGD, 2019, CELL MOL LIFE SCI, V76, P837, DOI 10.1007/s00018-018-2963-0
- DeBerardinis RJ, 2012, CELL, V148, P1132, DOI 10.1016/j.cell.2012.02.032
- Delage B, 2010, INT J CANCER, V126, P2762, DOI 10.1002/ijc.25202
- Don SSL, 2019, CELL CYCLE, V18, P2447, DOI 10.1080/15384101.2019.1648957
- Dossus L, 2021, GYNECOL ONCOL, V162, P475, DOI 10.1016/j.ygyno.2021.06.001
- Eniu DT, 2019, SCAND J CLIN LAB INV, V79, P17, DOI 10.1080/00365513.2018.1542541
- FALKSON G, 1990, ONCOLOGY-BASEL, V47, P401
- Fouad YA, 2017, AM J CANCER RES, V7, P1016
- Gong Y, 2021, CELL METAB, V33, P51, DOI 10.1016/j.cmet.2020.10.012
- Gonzalez A, 2021, CANCERS, V13, DOI 10.3390/cancers13133263
- Govindarajah N, 2019, CRIT REV ONCOL HEMAT, V138, P104, DOI 10.1016/j.critrevonc.2019.03.018
- Gowda GAN, 2008, EXPERT REV MOL DIAGN, V8, P617, DOI 10.1586/14737159.8.5.617
- Gu Y, 2015, J TRANSL MED, V13, DOI 10.1186/s12967-015-0408-1
- Gutierrez-Monreal MA, 2016, CHRONOBIOL INT, V33, P392, DOI 10.3109/07420528.2016.1152976
- Harbeck N, 2019, NAT REV DIS PRIMERS, V5, DOI [10.1038/s41572-019-0111-2, 10.1038/s41572-019-0122-z]
- Hasan M, 2020, BREAST CANCER-BASIC, V14, DOI 10.1177/1178223420924634
- Hasan M, 2019, MOL PHARMACOL, V96, P272, DOI 10.1124/mol.119.116202
- Heiden MGV, 2009, SCIENCE, V324, P1029, DOI 10.1126/science.1160809
- Hevia D, 2017, INT J MOL SCI, V18, DOI 10.3390/ijms18081620
- Hill SM, 2015, ENDOCR-RELAT CANCER, V22, pR183, DOI 10.1530/ERC-15-0030
- His M, 2019, BMC MED, V17, DOI 10.1186/s12916-019-1408-4
- Jardim-Perassi BV, 2014, PLOS ONE, V9, DOI 10.1371/journal.pone.0085311
- Kompare M, 2008, SEMIN PEDIATR NEUROL, V15, P140, DOI 10.1016/j.spen.2008.05.008
- Krishnaiah SY, 2017, CELL METAB, V25, P1206, DOI 10.1016/j.cmet.2017.04.023
- Kubatka P, 2018, CRIT REV ONCOL HEMAT, V122, P133, DOI 10.1016/j.critrevonc.2017.12.018
- Laborda-Illanes A, 2021, CANCERS, V13, DOI 10.3390/cancers13133141
- Li HX, 2019, NAT MED, V25, P850, DOI 10.1038/s41591-019-0404-8
- Lin HH, 2018, FRONT ENDOCRINOL, V9, DOI 10.3389/fendo.2018.00219
- Lo C, 2020, J PROTEOME RES, V19, P4061, DOI 10.1021/acs.jproteome.0c00362
- Lu X, 2019, MOL CARCINOGEN, V58, P749, DOI 10.1002/mc.22967
- Mao LL, 2014, J PINEAL RES, V56, P246, DOI 10.1111/jpi.12117
- Maroufi NF, 2022, BREAST CANCER-TOKYO, V29, P260, DOI 10.1007/s12282-021-01310-4
- Medina MA, 2003, CRIT REV BIOCHEM MOL, V38, P23, DOI 10.1080/713609209
- Melone MAB, 2018, CELL DEATH DIS, V9, DOI 10.1038/s41419-018-0313-7
- Minami Y, 2009, P NATL ACAD SCI USA, V106, P9890, DOI 10.1073/pnas.0900617106
- Murata T, 2019, BREAST CANCER RES TR, V177, P591, DOI 10.1007/s10549-019-05330-9
- Nelson N, 2022, INT J MOL SCI, V23, DOI 10.3390/ijms23031331
- Pang ZQ, 2021, NUCLEIC ACIDS RES, V49, pW388, DOI 10.1093/nar/gkab382
- Patti GJ, 2012, NAT REV MOL CELL BIO, V13, P263, DOI 10.1038/nrm3314
- Paula R, 2022, SCI REP-UK, V12, DOI 10.1038/s41598-022-04994-6
- Pavlova NN, 2022, CELL METAB, V34, P355, DOI 10.1016/j.cmet.2022.01.007
- Poschke I, 2013, J TRANSL MED, V11, DOI 10.1186/1479-5876-11-290
- Qiu FM, 2014, SCI SIGNAL, V7, DOI 10.1126/scisignal.2004761
- Qiu YP, 2013, INT J MOL SCI, V14, P8047, DOI 10.3390/ijms14048047
- Reiter R, 2021, INT J MOL SCI, V22, DOI 10.3390/ijms222212494
- Reiter RJ, 2021, LIFE SCI, V278, DOI 10.1016/j.lfs.2021.119597
- Reiter RJ, 2020, CELL MOL LIFE SCI, V77, P2527, DOI 10.1007/s00018-019-03438-1
- Rodriguez C, 2021, J CELL PHYSIOL, V236, P27, DOI 10.1002/jcp.29886
- Rossetti S, 2012, CELL CYCLE, V11, P350, DOI 10.4161/cc.11.2.18792
- Sonehara NM, 2019, ONCOL LETT, V17, P1635, DOI 10.3892/ol.2018.9758
- Starruy J, 2014, BIOINFORMATICS, V30, P1331, DOI 10.1093/bioinformatics/btt772
- Strand E, 2019, METABOLITES, V9, DOI 10.3390/metabo9120302
- Sun CL, 2020, THERANOSTICS, V10, P7070, DOI 10.7150/thno.45543
- Takayama T, 2016, CLIN CHIM ACTA, V452, P18, DOI 10.1016/j.cca.2015.10.032
- Wang YT, 2018, CELL DEATH DIFFER, V25, P733, DOI 10.1038/s41418-017-0013-3
- Wu D, 2022, Nan Fang Yi Ke Da Xue Xue Bao, V42, P278, DOI 10.12122/j.issn.1673-4254.2022.02.16
- Xiang S, 2012, BREAST CANCER-BASIC, V6, P137, DOI 10.4137/BCBCR.S9673
- Yuan BW, 2019, INT J CANCER, V144, P2833, DOI 10.1002/ijc.31996
- Yuan L, 2002, MOL CELL ENDOCRINOL, V192, P147, DOI 10.1016/S0303-7207(02)00029-1
- Zhang S, 2020, CELL DEATH DIS, V11, DOI 10.1038/s41419-020-03106-4
- Zhang T, 2021, MOLECULES, V26, DOI 10.3390/molecules26071990
- Zheng KH, 2019, CELL DEATH DIS, V10, DOI 10.1038/s41419-019-1303-0