Role of the hybrid Bcr/Abl kinase in the pathogenesis of chronic myeloid leukemia lacking C-Abl and CXCR4 proteins

Philadelphia chromosome is a result of chromosomal rearrangement that leads to the appearing of the hybrid gene bcr/abl. A hybrid mRNA transcribes from bcr-promoter and many copies of hybrid molecules of Bcr/Abl protein are formed as a result of bcr/abl gene expression. It is supposed that a hybrid...

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Veröffentlicht in:Experimental Oncology
Datum:2014
Hauptverfasser: Polishchuk, L.A., Telegeev, G.D.
Format: Artikel
Sprache:Englisch
Veröffentlicht: Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України 2014
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Online Zugang:https://nasplib.isofts.kiev.ua/handle/123456789/145357
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Zitieren:Role of the hybrid Bcr/Abl kinase in the pathogenesis of chronic myeloid leukemia lacking C-Abl and CXCR4 proteins / // Experimental Oncology. — 2014. — Т. 36, № 3. — С. 138-143. — Бібліогр.: 53 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
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author Polishchuk, L.A.
Telegeev, G.D.
author_facet Polishchuk, L.A.
Telegeev, G.D.
citation_txt Role of the hybrid Bcr/Abl kinase in the pathogenesis of chronic myeloid leukemia lacking C-Abl and CXCR4 proteins / // Experimental Oncology. — 2014. — Т. 36, № 3. — С. 138-143. — Бібліогр.: 53 назв. — англ.
collection DSpace DC
container_title Experimental Oncology
description Philadelphia chromosome is a result of chromosomal rearrangement that leads to the appearing of the hybrid gene bcr/abl. A hybrid mRNA transcribes from bcr-promoter and many copies of hybrid molecules of Bcr/Abl protein are formed as a result of bcr/abl gene expression. It is supposed that a hybrid Abl molecule, replacing the normal one, in majority of cases functions abnormally or does not function at all. Also it is possible that Abl moiety of Bcr/Abl protein which is possibly recognized by some hypothetical cell control system interpreted by cell as an overproduction of c-abl. This, probably, leads to blocking the normal C-Abl molecules production from the normal c-abl gene transcribed from the second non-aberrant chromosome 9. Based on C-Abl physiological functions in conjunction with the most important proteins of which functions directly depend on its activity we tried to outline the research directions that might explain disruptions of the processes at chronic myeloleukosis such as cell migration due to CXCL12/CXCR4 axis activation, reparation, apoptosis, control for mitochondria state, and to propose new perspective therapeutic approaches based on all this knowledge. Key Words: Bcr/Abl, CXCR4, C-Abl, chemokine, CXCL12.
first_indexed 2025-12-07T19:26:14Z
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last_indexed 2025-12-07T19:26:14Z
publishDate 2014
publisher Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України
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spelling Polishchuk, L.A.
Telegeev, G.D.
2019-01-20T19:25:49Z
2019-01-20T19:25:49Z
2014
Role of the hybrid Bcr/Abl kinase in the pathogenesis of chronic myeloid leukemia lacking C-Abl and CXCR4 proteins / // Experimental Oncology. — 2014. — Т. 36, № 3. — С. 138-143. — Бібліогр.: 53 назв. — англ.
1812-9269
https://nasplib.isofts.kiev.ua/handle/123456789/145357
Philadelphia chromosome is a result of chromosomal rearrangement that leads to the appearing of the hybrid gene bcr/abl. A hybrid mRNA transcribes from bcr-promoter and many copies of hybrid molecules of Bcr/Abl protein are formed as a result of bcr/abl gene expression. It is supposed that a hybrid Abl molecule, replacing the normal one, in majority of cases functions abnormally or does not function at all. Also it is possible that Abl moiety of Bcr/Abl protein which is possibly recognized by some hypothetical cell control system interpreted by cell as an overproduction of c-abl. This, probably, leads to blocking the normal C-Abl molecules production from the normal c-abl gene transcribed from the second non-aberrant chromosome 9. Based on C-Abl physiological functions in conjunction with the most important proteins of which functions directly depend on its activity we tried to outline the research directions that might explain disruptions of the processes at chronic myeloleukosis such as cell migration due to CXCL12/CXCR4 axis activation, reparation, apoptosis, control for mitochondria state, and to propose new perspective therapeutic approaches based on all this knowledge. Key Words: Bcr/Abl, CXCR4, C-Abl, chemokine, CXCL12.
en
Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України
Experimental Oncology
Reviews
Role of the hybrid Bcr/Abl kinase in the pathogenesis of chronic myeloid leukemia lacking C-Abl and CXCR4 proteins
Article
published earlier
spellingShingle Role of the hybrid Bcr/Abl kinase in the pathogenesis of chronic myeloid leukemia lacking C-Abl and CXCR4 proteins
Polishchuk, L.A.
Telegeev, G.D.
Reviews
title Role of the hybrid Bcr/Abl kinase in the pathogenesis of chronic myeloid leukemia lacking C-Abl and CXCR4 proteins
title_full Role of the hybrid Bcr/Abl kinase in the pathogenesis of chronic myeloid leukemia lacking C-Abl and CXCR4 proteins
title_fullStr Role of the hybrid Bcr/Abl kinase in the pathogenesis of chronic myeloid leukemia lacking C-Abl and CXCR4 proteins
title_full_unstemmed Role of the hybrid Bcr/Abl kinase in the pathogenesis of chronic myeloid leukemia lacking C-Abl and CXCR4 proteins
title_short Role of the hybrid Bcr/Abl kinase in the pathogenesis of chronic myeloid leukemia lacking C-Abl and CXCR4 proteins
title_sort role of the hybrid bcr/abl kinase in the pathogenesis of chronic myeloid leukemia lacking c-abl and cxcr4 proteins
topic Reviews
topic_facet Reviews
url https://nasplib.isofts.kiev.ua/handle/123456789/145357
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AT telegeevgd roleofthehybridbcrablkinaseinthepathogenesisofchronicmyeloidleukemialackingcablandcxcr4proteins