Loading…
Nature and importance of follicular lymphoma precursors
It is now widely recognized that cancer development is a protracted process requiring the stepwise acquisition of multiple oncogenic events. In humans, this process can take decades, if not a lifetime, blurring the notion of 'healthy' individuals. Follicular lymphoma exemplifies this multi...
Saved in:
Published in: | Haematologica (Roma) 2014-05, Vol.99 (5), p.802-810 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | 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-c574t-a128903566f1e09d33ad49144208ea0d7e270487ab26db867a7febb942507d483 |
---|---|
cites | |
container_end_page | 810 |
container_issue | 5 |
container_start_page | 802 |
container_title | Haematologica (Roma) |
container_volume | 99 |
creator | Mamessier, Emilie Broussais-Guillaumot, Florence Chetaille, Bruno Bouabdallah, Reda Xerri, Luc Jaffe, Elaine S Nadel, Bertrand |
description | It is now widely recognized that cancer development is a protracted process requiring the stepwise acquisition of multiple oncogenic events. In humans, this process can take decades, if not a lifetime, blurring the notion of 'healthy' individuals. Follicular lymphoma exemplifies this multistep pathway of oncogenesis. In recent years, variants of follicular lymphoma have been recognized that appear to represent clonal B-cell expansions at an early stage of follicular lymphoma lymphomagenesis. These include follicular lymphoma in situ, duodenal follicular lymphoma, partial involvement by follicular lymphoma, and in the blood circulating follicular lymphoma-like B cells. Recent genetic studies have identified similarities and differences between the early lesions and overt follicular lymphoma, providing important information for understanding their biological evolution. The data indicate that there is already genomic instability at these early stages, even in instances with a low risk for clinical progression. The overexpression of BCL2 in t(14;18)-positive B cells puts them at risk for subsequent genetic aberrations when they re-enter the germinal center and are exposed to the influences of activation-induced cytidine deaminase and somatic hypermutations. The emerging data provide a rationale for clinical management and, in the future, may identify genetic risk factors that warrant early therapeutic intervention. |
doi_str_mv | 10.3324/haematol.2013.085548 |
format | article |
fullrecord | <record><control><sourceid>pubmed_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_8aaf764fbe44462db85b0164f7342f61</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_8aaf764fbe44462db85b0164f7342f61</doaj_id><sourcerecordid>24790058</sourcerecordid><originalsourceid>FETCH-LOGICAL-c574t-a128903566f1e09d33ad49144208ea0d7e270487ab26db867a7febb942507d483</originalsourceid><addsrcrecordid>eNpdkU1r3DAQhkVp6G42_Qel-NqDtyNprI9LIYSmCSzJJTmLsS1lHeyVkb2B_Pt642bJ9iR4Ne8zEg9j3zispRT4c0u-ozG2awFcrsEUBZpPbMkLK3KjBf_MliAt5Aq0WbDzYXgGEGCt_sIWArUFKMyS6Tsa98lntKuzputjGmlX-SyGLMS2bap9SylrX7t-GzvK-uSrfRpiGi7YWaB28F__nSv2eP374eom39z_ub263ORVoXHMiQtjQRZKBe7B1lJSjZYjCjCeoNZeaECjqRSqLo3SpIMvS4uiAF2jkSt2O3PrSM-uT01H6dVFatxbENOTozQ2VeudIQpaYSg9Iiox4YoS-BRoiSIoPrF-zax-X3a-rvxuTNSeQE9vds3WPcUXhwCGczkBfsyA7X-1m8uNO2TTT41Eo14Oy3CerVIchuTDscDBHQS6d4HuINDNAqfa949vPJbejcm_soqYhg</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Nature and importance of follicular lymphoma precursors</title><source>Open Access: PubMed Central</source><source>Freely Accessible Science Journals</source><creator>Mamessier, Emilie ; Broussais-Guillaumot, Florence ; Chetaille, Bruno ; Bouabdallah, Reda ; Xerri, Luc ; Jaffe, Elaine S ; Nadel, Bertrand</creator><creatorcontrib>Mamessier, Emilie ; Broussais-Guillaumot, Florence ; Chetaille, Bruno ; Bouabdallah, Reda ; Xerri, Luc ; Jaffe, Elaine S ; Nadel, Bertrand</creatorcontrib><description>It is now widely recognized that cancer development is a protracted process requiring the stepwise acquisition of multiple oncogenic events. In humans, this process can take decades, if not a lifetime, blurring the notion of 'healthy' individuals. Follicular lymphoma exemplifies this multistep pathway of oncogenesis. In recent years, variants of follicular lymphoma have been recognized that appear to represent clonal B-cell expansions at an early stage of follicular lymphoma lymphomagenesis. These include follicular lymphoma in situ, duodenal follicular lymphoma, partial involvement by follicular lymphoma, and in the blood circulating follicular lymphoma-like B cells. Recent genetic studies have identified similarities and differences between the early lesions and overt follicular lymphoma, providing important information for understanding their biological evolution. The data indicate that there is already genomic instability at these early stages, even in instances with a low risk for clinical progression. The overexpression of BCL2 in t(14;18)-positive B cells puts them at risk for subsequent genetic aberrations when they re-enter the germinal center and are exposed to the influences of activation-induced cytidine deaminase and somatic hypermutations. The emerging data provide a rationale for clinical management and, in the future, may identify genetic risk factors that warrant early therapeutic intervention.</description><identifier>ISSN: 0390-6078</identifier><identifier>EISSN: 1592-8721</identifier><identifier>DOI: 10.3324/haematol.2013.085548</identifier><identifier>PMID: 24790058</identifier><language>eng</language><publisher>Italy: Ferrata Storti Foundation</publisher><subject>Cancer ; Cell Transformation, Neoplastic ; Humans ; Immunology ; Immunotherapy ; Life Sciences ; Lymphoma, Follicular - diagnosis ; Lymphoma, Follicular - etiology ; Lymphoma, Follicular - pathology ; Lymphoma, Follicular - therapy ; Precancerous Conditions ; Review</subject><ispartof>Haematologica (Roma), 2014-05, Vol.99 (5), p.802-810</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright© Ferrata Storti Foundation 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c574t-a128903566f1e09d33ad49144208ea0d7e270487ab26db867a7febb942507d483</citedby><orcidid>0000-0002-3516-0093</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/PMC4008113/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008113/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24790058$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03583486$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Mamessier, Emilie</creatorcontrib><creatorcontrib>Broussais-Guillaumot, Florence</creatorcontrib><creatorcontrib>Chetaille, Bruno</creatorcontrib><creatorcontrib>Bouabdallah, Reda</creatorcontrib><creatorcontrib>Xerri, Luc</creatorcontrib><creatorcontrib>Jaffe, Elaine S</creatorcontrib><creatorcontrib>Nadel, Bertrand</creatorcontrib><title>Nature and importance of follicular lymphoma precursors</title><title>Haematologica (Roma)</title><addtitle>Haematologica</addtitle><description>It is now widely recognized that cancer development is a protracted process requiring the stepwise acquisition of multiple oncogenic events. In humans, this process can take decades, if not a lifetime, blurring the notion of 'healthy' individuals. Follicular lymphoma exemplifies this multistep pathway of oncogenesis. In recent years, variants of follicular lymphoma have been recognized that appear to represent clonal B-cell expansions at an early stage of follicular lymphoma lymphomagenesis. These include follicular lymphoma in situ, duodenal follicular lymphoma, partial involvement by follicular lymphoma, and in the blood circulating follicular lymphoma-like B cells. Recent genetic studies have identified similarities and differences between the early lesions and overt follicular lymphoma, providing important information for understanding their biological evolution. The data indicate that there is already genomic instability at these early stages, even in instances with a low risk for clinical progression. The overexpression of BCL2 in t(14;18)-positive B cells puts them at risk for subsequent genetic aberrations when they re-enter the germinal center and are exposed to the influences of activation-induced cytidine deaminase and somatic hypermutations. The emerging data provide a rationale for clinical management and, in the future, may identify genetic risk factors that warrant early therapeutic intervention.</description><subject>Cancer</subject><subject>Cell Transformation, Neoplastic</subject><subject>Humans</subject><subject>Immunology</subject><subject>Immunotherapy</subject><subject>Life Sciences</subject><subject>Lymphoma, Follicular - diagnosis</subject><subject>Lymphoma, Follicular - etiology</subject><subject>Lymphoma, Follicular - pathology</subject><subject>Lymphoma, Follicular - therapy</subject><subject>Precancerous Conditions</subject><subject>Review</subject><issn>0390-6078</issn><issn>1592-8721</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpdkU1r3DAQhkVp6G42_Qel-NqDtyNprI9LIYSmCSzJJTmLsS1lHeyVkb2B_Pt642bJ9iR4Ne8zEg9j3zispRT4c0u-ozG2awFcrsEUBZpPbMkLK3KjBf_MliAt5Aq0WbDzYXgGEGCt_sIWArUFKMyS6Tsa98lntKuzputjGmlX-SyGLMS2bap9SylrX7t-GzvK-uSrfRpiGi7YWaB28F__nSv2eP374eom39z_ub263ORVoXHMiQtjQRZKBe7B1lJSjZYjCjCeoNZeaECjqRSqLo3SpIMvS4uiAF2jkSt2O3PrSM-uT01H6dVFatxbENOTozQ2VeudIQpaYSg9Iiox4YoS-BRoiSIoPrF-zax-X3a-rvxuTNSeQE9vds3WPcUXhwCGczkBfsyA7X-1m8uNO2TTT41Eo14Oy3CerVIchuTDscDBHQS6d4HuINDNAqfa949vPJbejcm_soqYhg</recordid><startdate>20140501</startdate><enddate>20140501</enddate><creator>Mamessier, Emilie</creator><creator>Broussais-Guillaumot, Florence</creator><creator>Chetaille, Bruno</creator><creator>Bouabdallah, Reda</creator><creator>Xerri, Luc</creator><creator>Jaffe, Elaine S</creator><creator>Nadel, Bertrand</creator><general>Ferrata Storti Foundation</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>1XC</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3516-0093</orcidid></search><sort><creationdate>20140501</creationdate><title>Nature and importance of follicular lymphoma precursors</title><author>Mamessier, Emilie ; Broussais-Guillaumot, Florence ; Chetaille, Bruno ; Bouabdallah, Reda ; Xerri, Luc ; Jaffe, Elaine S ; Nadel, Bertrand</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c574t-a128903566f1e09d33ad49144208ea0d7e270487ab26db867a7febb942507d483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Cancer</topic><topic>Cell Transformation, Neoplastic</topic><topic>Humans</topic><topic>Immunology</topic><topic>Immunotherapy</topic><topic>Life Sciences</topic><topic>Lymphoma, Follicular - diagnosis</topic><topic>Lymphoma, Follicular - etiology</topic><topic>Lymphoma, Follicular - pathology</topic><topic>Lymphoma, Follicular - therapy</topic><topic>Precancerous Conditions</topic><topic>Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mamessier, Emilie</creatorcontrib><creatorcontrib>Broussais-Guillaumot, Florence</creatorcontrib><creatorcontrib>Chetaille, Bruno</creatorcontrib><creatorcontrib>Bouabdallah, Reda</creatorcontrib><creatorcontrib>Xerri, Luc</creatorcontrib><creatorcontrib>Jaffe, Elaine S</creatorcontrib><creatorcontrib>Nadel, Bertrand</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Haematologica (Roma)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mamessier, Emilie</au><au>Broussais-Guillaumot, Florence</au><au>Chetaille, Bruno</au><au>Bouabdallah, Reda</au><au>Xerri, Luc</au><au>Jaffe, Elaine S</au><au>Nadel, Bertrand</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nature and importance of follicular lymphoma precursors</atitle><jtitle>Haematologica (Roma)</jtitle><addtitle>Haematologica</addtitle><date>2014-05-01</date><risdate>2014</risdate><volume>99</volume><issue>5</issue><spage>802</spage><epage>810</epage><pages>802-810</pages><issn>0390-6078</issn><eissn>1592-8721</eissn><abstract>It is now widely recognized that cancer development is a protracted process requiring the stepwise acquisition of multiple oncogenic events. In humans, this process can take decades, if not a lifetime, blurring the notion of 'healthy' individuals. Follicular lymphoma exemplifies this multistep pathway of oncogenesis. In recent years, variants of follicular lymphoma have been recognized that appear to represent clonal B-cell expansions at an early stage of follicular lymphoma lymphomagenesis. These include follicular lymphoma in situ, duodenal follicular lymphoma, partial involvement by follicular lymphoma, and in the blood circulating follicular lymphoma-like B cells. Recent genetic studies have identified similarities and differences between the early lesions and overt follicular lymphoma, providing important information for understanding their biological evolution. The data indicate that there is already genomic instability at these early stages, even in instances with a low risk for clinical progression. The overexpression of BCL2 in t(14;18)-positive B cells puts them at risk for subsequent genetic aberrations when they re-enter the germinal center and are exposed to the influences of activation-induced cytidine deaminase and somatic hypermutations. The emerging data provide a rationale for clinical management and, in the future, may identify genetic risk factors that warrant early therapeutic intervention.</abstract><cop>Italy</cop><pub>Ferrata Storti Foundation</pub><pmid>24790058</pmid><doi>10.3324/haematol.2013.085548</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-3516-0093</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0390-6078 |
ispartof | Haematologica (Roma), 2014-05, Vol.99 (5), p.802-810 |
issn | 0390-6078 1592-8721 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_8aaf764fbe44462db85b0164f7342f61 |
source | Open Access: PubMed Central; Freely Accessible Science Journals |
subjects | Cancer Cell Transformation, Neoplastic Humans Immunology Immunotherapy Life Sciences Lymphoma, Follicular - diagnosis Lymphoma, Follicular - etiology Lymphoma, Follicular - pathology Lymphoma, Follicular - therapy Precancerous Conditions Review |
title | Nature and importance of follicular lymphoma precursors |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T01%3A57%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Nature%20and%20importance%20of%20follicular%20lymphoma%20precursors&rft.jtitle=Haematologica%20(Roma)&rft.au=Mamessier,%20Emilie&rft.date=2014-05-01&rft.volume=99&rft.issue=5&rft.spage=802&rft.epage=810&rft.pages=802-810&rft.issn=0390-6078&rft.eissn=1592-8721&rft_id=info:doi/10.3324/haematol.2013.085548&rft_dat=%3Cpubmed_doaj_%3E24790058%3C/pubmed_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c574t-a128903566f1e09d33ad49144208ea0d7e270487ab26db867a7febb942507d483%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/24790058&rfr_iscdi=true |