Tightly-bound to DNA proteins in rat experimental hepatomas and normal liver cells

Proteins tightly bound to DNA (TBP) comprise a group of proteins that remain bound to DNA even after harsh deproteinization procedures. The amount of these proteins is 20–100 µg for mg of DNA depending on eukaryotic source. This experimental paper examines the possibility to use some TBP for clinica...

Повний опис

Збережено в:
Бібліографічні деталі
Дата:2011
Автори: Labeikyte, D., Borutinskaite, V., Legzdins, N., Sjakste, N.
Формат: Стаття
Мова:English
Опубліковано: Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України 2011
Назва видання:Experimental Oncology
Теми:
Онлайн доступ:http://dspace.nbuv.gov.ua/handle/123456789/138657
Теги: Додати тег
Немає тегів, Будьте першим, хто поставить тег для цього запису!
Назва журналу:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Цитувати:Tightly-bound to DNA proteins in rat experimental hepatomas and normal liver cells / D. Labeikyte, V. Borutinskaite, N. Legzdins, N. Sjakste // Experimental Oncology. — 2011. — Т. 33, № 3. — С. 121-125. — Бібліогр.: 30 назв. — англ.

Репозитарії

Digital Library of Periodicals of National Academy of Sciences of Ukraine
id irk-123456789-138657
record_format dspace
spelling irk-123456789-1386572018-06-20T03:08:36Z Tightly-bound to DNA proteins in rat experimental hepatomas and normal liver cells Labeikyte, D. Borutinskaite, V. Legzdins, N. Sjakste, N. Original contributions Proteins tightly bound to DNA (TBP) comprise a group of proteins that remain bound to DNA even after harsh deproteinization procedures. The amount of these proteins is 20–100 µg for mg of DNA depending on eukaryotic source. This experimental paper examines the possibility to use some TBP for clinical biomarker discovery, e.g. for identification of prognostic and diagnostic cancer markers. The main aim of this study was to designate differences between tightly DNA binding protein patterns extracted from rat liver and rat experimental hepatomas (Zajdela ascites hepatoma and hepatoma G-27) and to evaluate possibility that some of these proteins may be used as biomarkers for cell cancer transformation. Methods: We used proteomics aproach as a tool for comparison of pattern of TBP from rat experimental hepatomas and normal liver cells. Combination of 2DE fractionation with mass spectrometry (MALDI TOF-MS) suitable for parallel profiling of complex TBP mixtures. Results: Intriguingly 2DE protein maps of TBP from rat liver and rat experimental hepatomas (Zajdela acites hepatoma and hepatoma G-27) were quite different. We identified 9 proteins, some of them shared in all TBP patterns. Among identified tightly bound to DNA proteins there were three proteins considered as nuclear matrix proteins (lamin B1, scaffold attachment factor B1, heterogeneous nuclear ribonucleoprotein). Also we identified DNA repair protein RAD50, coiled-coil domain-containing protein 41, structural maintenance of chromosomes protein1A and some ATP –dependent RNA helicases indicating that TBP are of interest with respect to their potential involvement in the topological organization and/or function of genomic DNA. Conclusions: We suppose that proteomic approach for TBP identification may be promising in development of biomarkers, also obtained results may be valuable for further understanding TBP functions in genome. 2011 Article Tightly-bound to DNA proteins in rat experimental hepatomas and normal liver cells / D. Labeikyte, V. Borutinskaite, N. Legzdins, N. Sjakste // Experimental Oncology. — 2011. — Т. 33, № 3. — С. 121-125. — Бібліогр.: 30 назв. — англ. 1812-9269 http://dspace.nbuv.gov.ua/handle/123456789/138657 en Experimental Oncology Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України
institution Digital Library of Periodicals of National Academy of Sciences of Ukraine
collection DSpace DC
language English
topic Original contributions
Original contributions
spellingShingle Original contributions
Original contributions
Labeikyte, D.
Borutinskaite, V.
Legzdins, N.
Sjakste, N.
Tightly-bound to DNA proteins in rat experimental hepatomas and normal liver cells
Experimental Oncology
description Proteins tightly bound to DNA (TBP) comprise a group of proteins that remain bound to DNA even after harsh deproteinization procedures. The amount of these proteins is 20–100 µg for mg of DNA depending on eukaryotic source. This experimental paper examines the possibility to use some TBP for clinical biomarker discovery, e.g. for identification of prognostic and diagnostic cancer markers. The main aim of this study was to designate differences between tightly DNA binding protein patterns extracted from rat liver and rat experimental hepatomas (Zajdela ascites hepatoma and hepatoma G-27) and to evaluate possibility that some of these proteins may be used as biomarkers for cell cancer transformation. Methods: We used proteomics aproach as a tool for comparison of pattern of TBP from rat experimental hepatomas and normal liver cells. Combination of 2DE fractionation with mass spectrometry (MALDI TOF-MS) suitable for parallel profiling of complex TBP mixtures. Results: Intriguingly 2DE protein maps of TBP from rat liver and rat experimental hepatomas (Zajdela acites hepatoma and hepatoma G-27) were quite different. We identified 9 proteins, some of them shared in all TBP patterns. Among identified tightly bound to DNA proteins there were three proteins considered as nuclear matrix proteins (lamin B1, scaffold attachment factor B1, heterogeneous nuclear ribonucleoprotein). Also we identified DNA repair protein RAD50, coiled-coil domain-containing protein 41, structural maintenance of chromosomes protein1A and some ATP –dependent RNA helicases indicating that TBP are of interest with respect to their potential involvement in the topological organization and/or function of genomic DNA. Conclusions: We suppose that proteomic approach for TBP identification may be promising in development of biomarkers, also obtained results may be valuable for further understanding TBP functions in genome.
format Article
author Labeikyte, D.
Borutinskaite, V.
Legzdins, N.
Sjakste, N.
author_facet Labeikyte, D.
Borutinskaite, V.
Legzdins, N.
Sjakste, N.
author_sort Labeikyte, D.
title Tightly-bound to DNA proteins in rat experimental hepatomas and normal liver cells
title_short Tightly-bound to DNA proteins in rat experimental hepatomas and normal liver cells
title_full Tightly-bound to DNA proteins in rat experimental hepatomas and normal liver cells
title_fullStr Tightly-bound to DNA proteins in rat experimental hepatomas and normal liver cells
title_full_unstemmed Tightly-bound to DNA proteins in rat experimental hepatomas and normal liver cells
title_sort tightly-bound to dna proteins in rat experimental hepatomas and normal liver cells
publisher Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України
publishDate 2011
topic_facet Original contributions
url http://dspace.nbuv.gov.ua/handle/123456789/138657
citation_txt Tightly-bound to DNA proteins in rat experimental hepatomas and normal liver cells / D. Labeikyte, V. Borutinskaite, N. Legzdins, N. Sjakste // Experimental Oncology. — 2011. — Т. 33, № 3. — С. 121-125. — Бібліогр.: 30 назв. — англ.
series Experimental Oncology
work_keys_str_mv AT labeikyted tightlyboundtodnaproteinsinratexperimentalhepatomasandnormallivercells
AT borutinskaitev tightlyboundtodnaproteinsinratexperimentalhepatomasandnormallivercells
AT legzdinsn tightlyboundtodnaproteinsinratexperimentalhepatomasandnormallivercells
AT sjaksten tightlyboundtodnaproteinsinratexperimentalhepatomasandnormallivercells
first_indexed 2023-10-18T21:18:52Z
last_indexed 2023-10-18T21:18:52Z
_version_ 1796152483117006848