مورد إلكتروني

Bone marrow stroma damage induced by chemotherapy for acute lymphoblastic leukemia in children

التفاصيل البيبلوغرافية
العنوان: Bone marrow stroma damage induced by chemotherapy for acute lymphoblastic leukemia in children
المصدر: Pediatric research, 55 (1
بيانات النشر: 2004-01
تفاصيل مُضافة: Corazza, Francis
Hermans, Christophe
Ferster, Alina
Fondu, Pierre
Demulder, Anne
Sariban, Eric
نوع الوثيقة: Electronic Resource
مستخلص: Several studies have suggested a role of bone marrow stroma injury in long-term chemotherapy-induced hematopoietic failure. To evaluate whether bone marrow microenvironment is altered by chemotherapy for acute lymphoblastic leukemia (ALL) and to determine its contribution to postchemotherapy anemia, we investigated the ability of stroma from children receiving maintenance chemotherapy for ALL to support hematopoiesis. Long-term bone marrow cultures (LTBMC) were established with bone marrow cells either from ALL children under therapy (n = 24) or from control subjects (n = 19). Nonadherent cells and colony forming units-granulocytic monocytic (CFU-GM) output in LTBMC did not differ between patients and controls. In contrast, burst forming unit-erythroid (BFU-E) numbers were lower in patient LTBMC (p = 0.013). Co-cultures of normal CD34+ cells and preformed patient or control stromas showed significantly reduced hematopoietic supportive capabilities of patient stromas: both CFU-GM and BFU-E were reduced (p = 0.002 and 0.046, respectively). In addition, supernatants (SN) of patients' LTBMC inhibited normal BFU-E growth compared with SN of normal LTBMC. Transforming growth factor (TGF)-beta1 levels were increased in patient cultures (p = 0.0039) and inversely correlated with BFU-E produced in LTBMC (r = -0.36, p = 0.04). Neutralization of TGF-beta1 significantly increased the BFU-E output of patient LTBMC (p = 0.0078). In contrast, macrophage inflammatory peptide (MIP)-1alpha levels were lower in SN of patients compared with controls (p = 0.015). Thus, chemotherapy for ALL induces functional deregulation within bone marrow stromal cells with an increase in the growth-inhibiting factor TGF-beta1, together with a decrease in MIP-1alpha, which might contribute to hematopoietic toxicity.
Journal Article
SCOPUS: ar.j
info:eu-repo/semantics/published
مصطلحات الفهرس: Sciences bio-médicales et agricoles, 6-Mercaptopurine -- adverse effects, Antibodies -- pharmacology, Antigens, CD34 -- metabolism, Antimetabolites, Antineoplastic -- adverse effects, Antineoplastic Combined Chemotherapy Protocols -- adverse effects, Bone Marrow Cells -- drug effects, Bone Marrow Cells -- pathology, Cells, Cultured, Chemokine CCL3, Chemokine CCL4, Child, Chronic Disease, Coculture Techniques, Cytokines -- immunology, Erythroid Precursor Cells -- drug effects, Erythroid Precursor Cells -- metabolism, Erythroid Precursor Cells -- pathology, Humans, Macrophage Inflammatory Proteins -- immunology, Methotrexate -- adverse effects, Myeloid Progenitor Cells -- drug effects, Myeloid Progenitor Cells -- metabolism, Myeloid Progenitor Cells -- pathology, Precursor Cell Lymphoblastic Leukemia-Lymphoma -- drug therapy, Precursor Cell Lymphoblastic Leukemia-Lymphoma -- pathology, Stromal Cells -- drug effects, Stromal Cells -- metabolism, Stromal Cells -- pathology, Transforming Growth Factor beta -- immunology, Transforming Growth Factor beta1, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article
URL: https://dipot.ulb.ac.be/dspace/bitstream/2013/51626/6/a6f011b7-84a7-422e-85c0-6a8d2cf99d67.txt
https://dipot.ulb.ac.be/dspace/bitstream/2013/51626/3/doi_26739.pdf
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/51626
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL
الإتاحة: Open access content. Open access content
2 full-text file(s): info:eu-repo/semantics/restrictedAccess | info:eu-repo/semantics/restrictedAccess
ملاحظة: 2 full-text file(s): application/pdf | application/pdf
English
أرقام أخرى: EQY oai:dipot.ulb.ac.be:2013/51626
uri/info:doi/10.1203/01.PDR.0000099773.71438.91
uri/info:pii/01.PDR.0000099773.71438.91
uri/info:pmid/14561785
uri/info:scp/0346992206
local/VX-004774
764594149
المصدر المساهم: UNIVERSITE LIBRE DE BRUXELLES
From OAIster®, provided by the OCLC Cooperative.
رقم الأكسشن: edsoai.ocn764594149
قاعدة البيانات: OAIster