Loading…
Drugging the unfolded protein response in acute leukemias
The unfolded protein response (UPR), an endoplasmic reticulum (ER) stress-induced signaling cascade, is mediated by three major stress sensors IRE-1α, PERK, and ATF6α. Studies described the UPR as a critical network in selection, adaptation, and survival of cancer cells. While previous reviews focus...
Saved in:
Published in: | Journal of hematology and oncology 2015-07, Vol.8 (1), p.87-87, Article 87 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c559t-9eacb5ff4b3c270b83127beb60aaa96642d04dc5945bd6faa1388a519c4708e93 |
---|---|
cites | cdi_FETCH-LOGICAL-c559t-9eacb5ff4b3c270b83127beb60aaa96642d04dc5945bd6faa1388a519c4708e93 |
container_end_page | 87 |
container_issue | 1 |
container_start_page | 87 |
container_title | Journal of hematology and oncology |
container_volume | 8 |
creator | Kharabi Masouleh, Behzad Chevet, Eric Panse, Jens Jost, Edgar O'Dwyer, Michael Bruemmendorf, Tim H Samali, Afshin |
description | The unfolded protein response (UPR), an endoplasmic reticulum (ER) stress-induced signaling cascade, is mediated by three major stress sensors IRE-1α, PERK, and ATF6α. Studies described the UPR as a critical network in selection, adaptation, and survival of cancer cells. While previous reviews focused mainly on solid cancer cells, in this review, we summarize the recent findings focusing on acute leukemias. We take into account the impact of the underlying genetic alterations of acute leukemia cells, the leukemia stem cell pool, and provide an outline on the current genetic, clinical, and therapeutic findings. Furthermore, we shed light on the important oncogene-specific regulation of individual UPR signaling branches and the therapeutic relevance of this information to answer the question if the UPR could be an attractive novel target in acute leukemias. |
doi_str_mv | 10.1186/s13045-015-0184-7 |
format | article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4504168</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A541577982</galeid><sourcerecordid>A541577982</sourcerecordid><originalsourceid>FETCH-LOGICAL-c559t-9eacb5ff4b3c270b83127beb60aaa96642d04dc5945bd6faa1388a519c4708e93</originalsourceid><addsrcrecordid>eNptkl2L1TAQhoso7rr6A7yRgiB60TWT5vNGOKwfKxzwRq9Dmk7brD3NMWkX_PemnHU9Z5EwZJg87yS8maJ4CeQSQIn3CWrCeEVgDcUq-ag4B8lFpSSlj4_ys-JZSjeECNCUPC3OqACpBYHzQn-MS9_7qS_nActl6sLYYlvuY5jRT2XEtA9TwjLn1i0zliMuP3HnbXpePOnsmPDF3X5R_Pj86fvVdbX99uXr1WZbOc71XGm0ruFdx5raUUkaVQOVDTaCWGu1EIy2hLWOa8abVnTWQq2U5aAdk0Shri-KD4e--6XZYetwmqMdzT76nY2_TbDenJ5MfjB9uDWMEwZC5QbvDg2GB7LrzdasNZLNlDWpbyGzb-8ui-HXgmk2O58cjqOdMCzJgNCSAtdEZPT1A_QmLHHKVhiQihKhuFb_qN6OaHz2N7_RrU3NhjPgUmpFM3X5HyqvNlvtwoSdz_UTwZsjwYB2nIcUxmX2-bdOQTiALoaUInb3DgAx6xCZwxBlE9ZQzMiseXXs-L3i79TUfwBFCb8Z</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1782068598</pqid></control><display><type>article</type><title>Drugging the unfolded protein response in acute leukemias</title><source>Open Access: PubMed Central</source><source>Publicly Available Content (ProQuest)</source><creator>Kharabi Masouleh, Behzad ; Chevet, Eric ; Panse, Jens ; Jost, Edgar ; O'Dwyer, Michael ; Bruemmendorf, Tim H ; Samali, Afshin</creator><creatorcontrib>Kharabi Masouleh, Behzad ; Chevet, Eric ; Panse, Jens ; Jost, Edgar ; O'Dwyer, Michael ; Bruemmendorf, Tim H ; Samali, Afshin</creatorcontrib><description>The unfolded protein response (UPR), an endoplasmic reticulum (ER) stress-induced signaling cascade, is mediated by three major stress sensors IRE-1α, PERK, and ATF6α. Studies described the UPR as a critical network in selection, adaptation, and survival of cancer cells. While previous reviews focused mainly on solid cancer cells, in this review, we summarize the recent findings focusing on acute leukemias. We take into account the impact of the underlying genetic alterations of acute leukemia cells, the leukemia stem cell pool, and provide an outline on the current genetic, clinical, and therapeutic findings. Furthermore, we shed light on the important oncogene-specific regulation of individual UPR signaling branches and the therapeutic relevance of this information to answer the question if the UPR could be an attractive novel target in acute leukemias.</description><identifier>ISSN: 1756-8722</identifier><identifier>EISSN: 1756-8722</identifier><identifier>DOI: 10.1186/s13045-015-0184-7</identifier><identifier>PMID: 26179601</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Acquisitions & mergers ; Cancer ; Cell Survival ; Funding ; Health aspects ; Hematology ; Homeostasis ; Humans ; Kinases ; Leukemia ; Leukemia - genetics ; Life Sciences ; Mutation ; Oncology ; Protein folding ; Review ; Signal Transduction ; Stem cells ; Studies ; Transcription factors ; Unfolded Protein Response - genetics</subject><ispartof>Journal of hematology and oncology, 2015-07, Vol.8 (1), p.87-87, Article 87</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2015</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Kharabi Masouleh et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c559t-9eacb5ff4b3c270b83127beb60aaa96642d04dc5945bd6faa1388a519c4708e93</citedby><cites>FETCH-LOGICAL-c559t-9eacb5ff4b3c270b83127beb60aaa96642d04dc5945bd6faa1388a519c4708e93</cites><orcidid>0000-0001-5855-4522</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504168/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1782068598?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26179601$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://univ-rennes.hal.science/hal-01187303$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Kharabi Masouleh, Behzad</creatorcontrib><creatorcontrib>Chevet, Eric</creatorcontrib><creatorcontrib>Panse, Jens</creatorcontrib><creatorcontrib>Jost, Edgar</creatorcontrib><creatorcontrib>O'Dwyer, Michael</creatorcontrib><creatorcontrib>Bruemmendorf, Tim H</creatorcontrib><creatorcontrib>Samali, Afshin</creatorcontrib><title>Drugging the unfolded protein response in acute leukemias</title><title>Journal of hematology and oncology</title><addtitle>J Hematol Oncol</addtitle><description>The unfolded protein response (UPR), an endoplasmic reticulum (ER) stress-induced signaling cascade, is mediated by three major stress sensors IRE-1α, PERK, and ATF6α. Studies described the UPR as a critical network in selection, adaptation, and survival of cancer cells. While previous reviews focused mainly on solid cancer cells, in this review, we summarize the recent findings focusing on acute leukemias. We take into account the impact of the underlying genetic alterations of acute leukemia cells, the leukemia stem cell pool, and provide an outline on the current genetic, clinical, and therapeutic findings. Furthermore, we shed light on the important oncogene-specific regulation of individual UPR signaling branches and the therapeutic relevance of this information to answer the question if the UPR could be an attractive novel target in acute leukemias.</description><subject>Acquisitions & mergers</subject><subject>Cancer</subject><subject>Cell Survival</subject><subject>Funding</subject><subject>Health aspects</subject><subject>Hematology</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Kinases</subject><subject>Leukemia</subject><subject>Leukemia - genetics</subject><subject>Life Sciences</subject><subject>Mutation</subject><subject>Oncology</subject><subject>Protein folding</subject><subject>Review</subject><subject>Signal Transduction</subject><subject>Stem cells</subject><subject>Studies</subject><subject>Transcription factors</subject><subject>Unfolded Protein Response - genetics</subject><issn>1756-8722</issn><issn>1756-8722</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptkl2L1TAQhoso7rr6A7yRgiB60TWT5vNGOKwfKxzwRq9Dmk7brD3NMWkX_PemnHU9Z5EwZJg87yS8maJ4CeQSQIn3CWrCeEVgDcUq-ag4B8lFpSSlj4_ys-JZSjeECNCUPC3OqACpBYHzQn-MS9_7qS_nActl6sLYYlvuY5jRT2XEtA9TwjLn1i0zliMuP3HnbXpePOnsmPDF3X5R_Pj86fvVdbX99uXr1WZbOc71XGm0ruFdx5raUUkaVQOVDTaCWGu1EIy2hLWOa8abVnTWQq2U5aAdk0Shri-KD4e--6XZYetwmqMdzT76nY2_TbDenJ5MfjB9uDWMEwZC5QbvDg2GB7LrzdasNZLNlDWpbyGzb-8ui-HXgmk2O58cjqOdMCzJgNCSAtdEZPT1A_QmLHHKVhiQihKhuFb_qN6OaHz2N7_RrU3NhjPgUmpFM3X5HyqvNlvtwoSdz_UTwZsjwYB2nIcUxmX2-bdOQTiALoaUInb3DgAx6xCZwxBlE9ZQzMiseXXs-L3i79TUfwBFCb8Z</recordid><startdate>20150716</startdate><enddate>20150716</enddate><creator>Kharabi Masouleh, Behzad</creator><creator>Chevet, Eric</creator><creator>Panse, Jens</creator><creator>Jost, Edgar</creator><creator>O'Dwyer, Michael</creator><creator>Bruemmendorf, Tim H</creator><creator>Samali, Afshin</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5855-4522</orcidid></search><sort><creationdate>20150716</creationdate><title>Drugging the unfolded protein response in acute leukemias</title><author>Kharabi Masouleh, Behzad ; Chevet, Eric ; Panse, Jens ; Jost, Edgar ; O'Dwyer, Michael ; Bruemmendorf, Tim H ; Samali, Afshin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c559t-9eacb5ff4b3c270b83127beb60aaa96642d04dc5945bd6faa1388a519c4708e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acquisitions & mergers</topic><topic>Cancer</topic><topic>Cell Survival</topic><topic>Funding</topic><topic>Health aspects</topic><topic>Hematology</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Kinases</topic><topic>Leukemia</topic><topic>Leukemia - genetics</topic><topic>Life Sciences</topic><topic>Mutation</topic><topic>Oncology</topic><topic>Protein folding</topic><topic>Review</topic><topic>Signal Transduction</topic><topic>Stem cells</topic><topic>Studies</topic><topic>Transcription factors</topic><topic>Unfolded Protein Response - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kharabi Masouleh, Behzad</creatorcontrib><creatorcontrib>Chevet, Eric</creatorcontrib><creatorcontrib>Panse, Jens</creatorcontrib><creatorcontrib>Jost, Edgar</creatorcontrib><creatorcontrib>O'Dwyer, Michael</creatorcontrib><creatorcontrib>Bruemmendorf, Tim H</creatorcontrib><creatorcontrib>Samali, Afshin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of hematology and oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kharabi Masouleh, Behzad</au><au>Chevet, Eric</au><au>Panse, Jens</au><au>Jost, Edgar</au><au>O'Dwyer, Michael</au><au>Bruemmendorf, Tim H</au><au>Samali, Afshin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Drugging the unfolded protein response in acute leukemias</atitle><jtitle>Journal of hematology and oncology</jtitle><addtitle>J Hematol Oncol</addtitle><date>2015-07-16</date><risdate>2015</risdate><volume>8</volume><issue>1</issue><spage>87</spage><epage>87</epage><pages>87-87</pages><artnum>87</artnum><issn>1756-8722</issn><eissn>1756-8722</eissn><abstract>The unfolded protein response (UPR), an endoplasmic reticulum (ER) stress-induced signaling cascade, is mediated by three major stress sensors IRE-1α, PERK, and ATF6α. Studies described the UPR as a critical network in selection, adaptation, and survival of cancer cells. While previous reviews focused mainly on solid cancer cells, in this review, we summarize the recent findings focusing on acute leukemias. We take into account the impact of the underlying genetic alterations of acute leukemia cells, the leukemia stem cell pool, and provide an outline on the current genetic, clinical, and therapeutic findings. Furthermore, we shed light on the important oncogene-specific regulation of individual UPR signaling branches and the therapeutic relevance of this information to answer the question if the UPR could be an attractive novel target in acute leukemias.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26179601</pmid><doi>10.1186/s13045-015-0184-7</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-5855-4522</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1756-8722 |
ispartof | Journal of hematology and oncology, 2015-07, Vol.8 (1), p.87-87, Article 87 |
issn | 1756-8722 1756-8722 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4504168 |
source | Open Access: PubMed Central; Publicly Available Content (ProQuest) |
subjects | Acquisitions & mergers Cancer Cell Survival Funding Health aspects Hematology Homeostasis Humans Kinases Leukemia Leukemia - genetics Life Sciences Mutation Oncology Protein folding Review Signal Transduction Stem cells Studies Transcription factors Unfolded Protein Response - genetics |
title | Drugging the unfolded protein response in acute leukemias |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T19%3A36%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Drugging%20the%20unfolded%20protein%20response%20in%20acute%20leukemias&rft.jtitle=Journal%20of%20hematology%20and%20oncology&rft.au=Kharabi%20Masouleh,%20Behzad&rft.date=2015-07-16&rft.volume=8&rft.issue=1&rft.spage=87&rft.epage=87&rft.pages=87-87&rft.artnum=87&rft.issn=1756-8722&rft.eissn=1756-8722&rft_id=info:doi/10.1186/s13045-015-0184-7&rft_dat=%3Cgale_pubme%3EA541577982%3C/gale_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c559t-9eacb5ff4b3c270b83127beb60aaa96642d04dc5945bd6faa1388a519c4708e93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1782068598&rft_id=info:pmid/26179601&rft_galeid=A541577982&rfr_iscdi=true |