Vascular calcification is a high incidence and high risk disease with increasing morbidity and high mortality, which is considered the consequence of smooth muscle cell transdifferentiation initiating the mechanism of accumulation of hydroxyl calcium phosphate. Vascular calcification is also thought to be strongly associated with poor outcomes in diabetes and chronic kidney disease. Numerous studies have been accomplished; however, the specific mechanism of the disease remains unclear. Development of the genome project enhanced the understanding of life science and has entered the post-genomic era resulting in a variety of omics techniques used in studies and a large amount of available data; thus, a new perspective on data analysis has been revealed. Omics has a broader perspective and is thus advantageous over a single pathway analysis in the study of complex vascular calcification mechanisms. This paper reviews in detail various omics studies including genomics, proteomics, transcriptomics, metabolomics and multiple group studies on vascular calcification. Advances and deficiencies in the use of omics to study vascular calcification are presented in a comprehensive view. We also review the methodology of the omics studies and omics data analysis and processing. In addition, the methodology and data processing presented here can be applied to other areas. An omics landscape perspective across the boundaries between genomics, transcriptomics, proteomics and metabolomics is used to examine the mechanisms of vascular calcification. The perspective combined with various technologies also provides a direction for the subsequent exploration of clinical significance.
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Russian Acad Sci, Inst Cytol, St Petersburg, Russia
Almazov Natl Med Res Ctr Russia, St Petersburg, RussiaRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Semenova, Daria
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Zabirnyk, Arsenii
Lobov, Arseniy
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Russian Acad Sci, Inst Cytol, St Petersburg, RussiaRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Lobov, Arseniy
Boyarskaya, Nadezda
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Almazov Natl Med Res Ctr Russia, St Petersburg, RussiaRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Boyarskaya, Nadezda
Kachanova, Olga
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Almazov Natl Med Res Ctr Russia, St Petersburg, RussiaRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Kachanova, Olga
Uspensky, Vladimir
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Almazov Natl Med Res Ctr Russia, St Petersburg, RussiaRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Uspensky, Vladimir
Zainullina, Bozhana
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St Petersburg State Univ, Ctr Mol & Cell Technol, St Petersburg, RussiaRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Zainullina, Bozhana
Denisov, Evgeny
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Russian Acad Sci, Canc Res Inst, Tomsk Natl Res Med Ctr, Lab Canc Progress Biol, Tomsk, RussiaRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Denisov, Evgeny
Gerashchenko, Tatiana
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Russian Acad Sci, Canc Res Inst, Tomsk Natl Res Med Ctr, Lab Canc Progress Biol, Tomsk, RussiaRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Gerashchenko, Tatiana
Kvitting, John-Peder Escobar
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Univ Oslo, Inst Basic Med Sci, Div Physiol, Heart Physiol Res Grp, Oslo, Norway
Oslo Univ Hosp, Oslo, NorwayRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Kvitting, John-Peder Escobar
Kaljusto, Mari-Liis
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Oslo Univ Hosp, Oslo, NorwayRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Kaljusto, Mari-Liis
Thiede, Bernd
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Univ Oslo, Inst Basic Med Sci, Div Physiol, Heart Physiol Res Grp, Oslo, NorwayRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Thiede, Bernd
Kostareva, Anna
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Almazov Natl Med Res Ctr Russia, St Petersburg, RussiaRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Kostareva, Anna
Stenslokken, Kare-Olav
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Univ Oslo, Inst Basic Med Sci, Div Physiol, Heart Physiol Res Grp, Oslo, NorwayRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Stenslokken, Kare-Olav
Vaage, Jarle
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Univ Oslo, Inst Basic Med Sci, Div Physiol, Heart Physiol Res Grp, Oslo, Norway
Oslo Univ Hosp, Oslo, NorwayRussian Acad Sci, Inst Cytol, St Petersburg, Russia
Vaage, Jarle
Malashicheva, Anna
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Russian Acad Sci, Inst Cytol, St Petersburg, RussiaRussian Acad Sci, Inst Cytol, St Petersburg, Russia
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UNSW Sydney, Adult Canc Program, Lowy Canc Res Ctr, Sydney, NSW 2052, Australia
UNSW Sydney, Prince Wales Clin Sch, Sydney, NSW 2052, AustraliaUniv Ghent, Dept Biomol Med, Ghent, Belgium
Anande, Govardhan
Thandapani, Palaniraja
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New York Univ, Dept Pathol, Sch Med, New York, NY USA
New York Univ, Sch Med, Laura & Isaac Perlmutter Canc Ctr, New York, NY USAUniv Ghent, Dept Biomol Med, Ghent, Belgium
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New York Univ, Dept Pathol, Sch Med, New York, NY USA
New York Univ, Sch Med, Laura & Isaac Perlmutter Canc Ctr, New York, NY USAUniv Ghent, Dept Biomol Med, Ghent, Belgium
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Chinese Acad Agr Sci, Biotechnol Res Inst, Beijing 100081, Peoples R ChinaChinese Acad Agr Sci, Biotechnol Res Inst, Beijing 100081, Peoples R China
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Univ Edinburgh, Wellcome Ctr Cell Biol, Michael Swann Bldg Max Born Crescent,Kings Bldg, Edinburgh EH9 3BF, ScotlandUniv Edinburgh, Wellcome Ctr Cell Biol, Michael Swann Bldg Max Born Crescent,Kings Bldg, Edinburgh EH9 3BF, Scotland
Dunn-Davies, Hywel
Dudnakova, Tatiana
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Univ Edinburgh, Wellcome Ctr Cell Biol, Michael Swann Bldg Max Born Crescent,Kings Bldg, Edinburgh EH9 3BF, ScotlandUniv Edinburgh, Wellcome Ctr Cell Biol, Michael Swann Bldg Max Born Crescent,Kings Bldg, Edinburgh EH9 3BF, Scotland
Dudnakova, Tatiana
Baker, Andrew H.
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Univ Edinburgh, Queens Med Res Inst QMRI, Ctr Cardiovasc Sci, 47 Little France Crescent, Edinburgh EH16 4TJ, ScotlandUniv Edinburgh, Wellcome Ctr Cell Biol, Michael Swann Bldg Max Born Crescent,Kings Bldg, Edinburgh EH9 3BF, Scotland
Baker, Andrew H.
Mitic, Tijana
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Univ Edinburgh, Queens Med Res Inst QMRI, Ctr Cardiovasc Sci, 47 Little France Crescent, Edinburgh EH16 4TJ, ScotlandUniv Edinburgh, Wellcome Ctr Cell Biol, Michael Swann Bldg Max Born Crescent,Kings Bldg, Edinburgh EH9 3BF, Scotland