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WFRF:(Tognon Gianluca 1976)
 

Sökning: WFRF:(Tognon Gianluca 1976) > Effect of Aplidin i...

Effect of Aplidin in acute lymphoblastic leukaemia cells.

Erba, E (författare)
Serafini, M (författare)
Gaipa, G (författare)
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Tognon, Gianluca, 1976 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin,Institute of Internal Medicine
Marchini, S (författare)
Celli, N (författare)
Rotilio, D (författare)
Broggini, M (författare)
Jimeno, J (författare)
Faircloth, G T (författare)
Biondi, A (författare)
D'Incalci, M (författare)
visa färre...
 (creator_code:org_t)
2003-08-12
2003
Engelska.
Ingår i: British journal of cancer. - : Springer Science and Business Media LLC. - 0007-0920 .- 1532-1827. ; 89:4, s. 763-73
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The cytotoxic effect of Aplidin was investigated on fresh leukaemia cells derived from children with B-cell-precursor (BCP) acute lymphoblastic leukaemia (ALL) by using stromal-layer culture system and on four cell lines, ALL-PO, Reh, ALL/MIK and TOM-1, derived from patients with ALL with different molecular genetic abnormalities. In ALL cell lines Aplidin was cytotoxic at nanomolar concentrations. In the ALL cell lines the drug-induced cell death was clearly related to the induction of apoptosis and appeared to be p53-independent. Only in ALL-PO 20 nM Aplidin treatment caused a block of vascular endothelial growth factor (VEGF) secretion and downregulation of VEGF-mRNA, but Aplidin cytotoxicity does not seem to be related to VEGF inhibition since the sensitivity of ALL-PO cells to Aplidin is comparable to that observed for the other cells used. Aplidin induced a G(1) and a G(2) M block in ALL cell lines. In patient-derived leukaemia cells, Aplidin induced a strong cytotoxicity evidenced in a stroma-supported immunocytometric assay. Cells from children with genetic abnormalities such as t(9;22) and t(4;11) translocations, associated with an inferior treatment outcome, were sensitive to Aplidin to the same extent as that observed in other BCP-ALL cases. Aplidin exerted a strong cell killing effect (>88%) against primary culture cells from five relapsed ALL cases, at concentrations much lower than those reported to be achieved in plasma of patients receiving Aplidin at recommended doses. Taken together these data suggest that Aplidin could be a new anticancer drug to be investigated in ALL patients resistant to available therapy.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Nyckelord

Adolescent
Antineoplastic Agents
pharmacology
Apoptosis
drug effects
B-Lymphocytes
drug effects
Caspase 3
Caspases
metabolism
Cell Cycle
drug effects
Child
Child
Preschool
Depsipeptides
Dose-Response Relationship
Drug
Drug Resistance
Neoplasm
Endothelial Growth Factors
genetics
metabolism
Female
Humans
Intercellular Signaling Peptides and Proteins
genetics
metabolism
Karyotyping
Lymphokines
genetics
metabolism
Male
Mass Spectrometry
Peptides
Cyclic
pharmacology
Precursor Cell Lymphoblastic Leukemia-Lymphoma
metabolism
pathology
RNA
Messenger
metabolism
RNA
Neoplasm
metabolism
Stromal Cells
drug effects
pathology
Tumor Cells
Cultured
Vascular Endothelial Growth Factor A
Vascular Endothelial Growth Factors

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