We have shown that human B-cell non-Hodgkin lymphomas (B-NHLs) express heat shock protein (HSP)H1/105 in function of their aggressiveness. Here, we now clarify its role as a functional B-NHL target by testing the hypothesis that it promotes the stabilization of key lymphoma oncoproteins. HSPH1 silencing in 4 models of aggressive B-NHLs was paralleled by Bcl-6 and c-Myc downregulation. In vitro and in vivo analysis of HSPH1-silenced Namalwa cells showed that this effect was associated with a significant growth delay and the loss of tumorigenicity when 10(4) cells were injected into mice. Interestingly, we found that HSPH1 physically interacts with c-Myc and Bcl-6 in both Namalwa cells and primary aggressive B-NHLs. Accordingly, expression of HSPH1 and either c-Myc or Bcl-6 positively correlated in these diseases. Our study indicates that HSPH1 concurrently favors the expression of 2 key lymphoma oncoproteins, thus confirming its candidacy as a valuable therapeutic target of aggressive B-NHLs.

HSP105 inhibition hampers the growth of human aggressive B-cell non-Hodgkin lymphoma by counteracting key oncogenic pathways / R. Zappasodi, A. Cavané, M. Tortoreto, C. Tringali, A.D. Cabras, G. Ruggiero, L. Castagnoli, B. Venerando, N. Zaffaroni, S.M. Pupa, A.M. Gianni, M. Di Nicola. - In: BONE MARROW TRANSPLANTATION. - ISSN 0268-3369. - 48:Suppl. 2(2013), pp. S431-S432. (Intervento presentato al 39. convegno Annual Meeting of the European Group for Blood and Marrow Transplantation tenutosi a London nel 2013) [10.1038/bmt.2013.23].

HSP105 inhibition hampers the growth of human aggressive B-cell non-Hodgkin lymphoma by counteracting key oncogenic pathways

A. Cavané
Secondo
;
C. Tringali;B. Venerando;A.M. Gianni
Penultimo
;
2013

Abstract

We have shown that human B-cell non-Hodgkin lymphomas (B-NHLs) express heat shock protein (HSP)H1/105 in function of their aggressiveness. Here, we now clarify its role as a functional B-NHL target by testing the hypothesis that it promotes the stabilization of key lymphoma oncoproteins. HSPH1 silencing in 4 models of aggressive B-NHLs was paralleled by Bcl-6 and c-Myc downregulation. In vitro and in vivo analysis of HSPH1-silenced Namalwa cells showed that this effect was associated with a significant growth delay and the loss of tumorigenicity when 10(4) cells were injected into mice. Interestingly, we found that HSPH1 physically interacts with c-Myc and Bcl-6 in both Namalwa cells and primary aggressive B-NHLs. Accordingly, expression of HSPH1 and either c-Myc or Bcl-6 positively correlated in these diseases. Our study indicates that HSPH1 concurrently favors the expression of 2 key lymphoma oncoproteins, thus confirming its candidacy as a valuable therapeutic target of aggressive B-NHLs.
No
English
Settore BIO/10 - Biochimica
Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica
Poster
Esperti anonimi
Pubblicazione scientifica
2013
48
Suppl. 2
S431
S432
2
Pubblicato
Periodico con rilevanza internazionale
Annual Meeting of the European Group for Blood and Marrow Transplantation
London
2013
39
Convegno internazionale
Intervento inviato
info:eu-repo/semantics/article
HSP105 inhibition hampers the growth of human aggressive B-cell non-Hodgkin lymphoma by counteracting key oncogenic pathways / R. Zappasodi, A. Cavané, M. Tortoreto, C. Tringali, A.D. Cabras, G. Ruggiero, L. Castagnoli, B. Venerando, N. Zaffaroni, S.M. Pupa, A.M. Gianni, M. Di Nicola. - In: BONE MARROW TRANSPLANTATION. - ISSN 0268-3369. - 48:Suppl. 2(2013), pp. S431-S432. (Intervento presentato al 39. convegno Annual Meeting of the European Group for Blood and Marrow Transplantation tenutosi a London nel 2013) [10.1038/bmt.2013.23].
reserved
Prodotti della ricerca::01 - Articolo su periodico
12
275
Article (author)
Periodico con Impact Factor
R. Zappasodi, A. Cavané, M. Tortoreto, C. Tringali, A.D. Cabras, G. Ruggiero, L. Castagnoli, B. Venerando, N. Zaffaroni, S.M. Pupa, A.M. Gianni, M. Di Nicola
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/225186
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