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Exploiting pleiotropic activities of semaphorins as multi-target therapies for cancer.

Moserle L, Casanovas O - EMBO Mol Med (2012)

View Article: PubMed Central - PubMed

Affiliation: Tumor Angiogenesis Group, Catalan Institute of Oncology - IDIBELL, L'Hospitalet de Llobregat, Spain.

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See related article in EMBO Molecular Medicine http://dx.doi.org/10.1002/emmm.201100205 Semaphorins (SEMAs) are a superfamily of secreted or membrane-associated glycoproteins implicated in the control of axonal wiring and involved in angiogenesis and cancer progression... The dual activities of p61-Sema3E depend on the specific transactivated molecules recruited by the complex Sema3E–PlxnD1 in the different types of cells... In endothelial cells, the intrinsic R-Ras GAP activity of PlxnD1 promotes a cell-collapsing response as well as an Arf6 GTPase-mediated integrin-beta1 endocytosis and decreased cellular adhesion to the extracellular matrix (Casazza et al, ; Sakurai et al, )... Molecularly, Casazza et al demonstrate that Uncl-Sema3E not only interferes with the endogenous Sema3E signalling, but is also unable to induce the association of PlxnD1 with ErbB2 in the tumour cell context... The study from Casazza et al points out a remarkable pleiotropic anti-cancer potential of Uncl-Sema3E but also reveals several relevant therapeutic opportunities dually targeting angiogenesis and invasion/metastasis. »The study from Casazza et al points out a remarkable pleiotropic anti-cancer potential of Uncl-Sema3E but also reveals several relevant therapeutic opportunities dually targeting angiogenesis and invasion/metastasis. « On the one hand, based on the observation that the uncleavable molecule demonstrates a dominant-negative function over the endogenous Sema3E signalling, one specific therapeutic approach could be the use of a recombinant Uncl-Sema3E as a drug that would maintain the known anti-angiogenic activity of Sema3E without activating the pro-invasive and pro-metastatic process... By inhibiting Furin the endogenous full-length Sema3E would not be effectively cleaved, and an uncleaved form would accumulate in Sema3E-expressing tumours... Uncleaved Sema3E accumulation by Furin inhibition would lead to the competitive blockage of p61-Sema3E pro-invasive and pro-metastatic activity without impairing the anti-angiogenic effects of cleaved Sema3E... To further support this possibility, Furin is frequently expressed in human cancers and its expression correlates with aggressiveness and metastasis, thus making it a potential target for anti-cancer therapies (Christensen et al, )... A crucial point in the putative applicability of Sema3E-related therapies is the critical functional link between Sema3E–PlxnD1 and its transactivated associated molecules... In the context of other anti-tumour therapies, the article from Casazza et al further emphasizes the need of a careful reflection on the use of anti-angiogenic therapy in the treatment of cancer... Due to the implication of different mechanisms involved in the spread of tumour cells promoted by these two distinct treatments, the inhibition of pro-invasive and pro-metastatic process by Uncl-Sema3E strongly supports a possible added therapeutic potential of this molecule in anti-VEGF/R treated tumours... Indeed, results from Casazza et al demonstrate Uncl-Sema3E anti-tumour activity is maintained in models refractory to VEGF therapy... Thus, further efforts have to be made to define the anti-cancer outcome of combinatorial Uncl-Sema3E together with standard anti-angiogenic therapy to determine whether there could be additive anti-angiogenic effects and compensatory anti-invasive and anti-metastatic effects.

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The multi-target effects of p61-Sema3E and uncleavable Sema3E (Uncl-Sema3E) in tumoursEndogenous Sema3E is converted by Furin-mediated cleavage in the active p61-Sema3E. In endothelial cells, its binding to PlxnD1 triggers the intrinsic R-Ras GAP activity of PlxnD1 and results in an anti-angiogenic effect due to the pro-apoptotic collapsing response and disassembly of focal adhesions. In tumour cells, binding of p61-Sema3E to PlxnD1 promotes the formation of a heteromultimeric complex with ErbB2 RTK that leads to its transactivation and further activation of ErbB2-EGFR-mediated pro-invasive and pro-metastatic signalling pathway.Uncl-Sema3E effectively competes with p61-Sema3E for the binding to PlxnD1. Upon binding, it induces PlxnD1 activation and triggers the same signalling molecules and anti-angiogenic effect on endothelial cells. On the contrary, in tumour cells, Uncl-Sema3E binding to PlxnD1 is unable to form a complex and activate the ErbB2-EGFR response, therefore, producing a anti-invasive and anti-metastatic effect.
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fig01: The multi-target effects of p61-Sema3E and uncleavable Sema3E (Uncl-Sema3E) in tumoursEndogenous Sema3E is converted by Furin-mediated cleavage in the active p61-Sema3E. In endothelial cells, its binding to PlxnD1 triggers the intrinsic R-Ras GAP activity of PlxnD1 and results in an anti-angiogenic effect due to the pro-apoptotic collapsing response and disassembly of focal adhesions. In tumour cells, binding of p61-Sema3E to PlxnD1 promotes the formation of a heteromultimeric complex with ErbB2 RTK that leads to its transactivation and further activation of ErbB2-EGFR-mediated pro-invasive and pro-metastatic signalling pathway.Uncl-Sema3E effectively competes with p61-Sema3E for the binding to PlxnD1. Upon binding, it induces PlxnD1 activation and triggers the same signalling molecules and anti-angiogenic effect on endothelial cells. On the contrary, in tumour cells, Uncl-Sema3E binding to PlxnD1 is unable to form a complex and activate the ErbB2-EGFR response, therefore, producing a anti-invasive and anti-metastatic effect.

Mentions: Sema3E is one of the SEMAs implicated in tumour invasion and metastatization and its expression correlates with the metastatic process. Sema3E is synthesized as a full-length precursor molecule and its proteolytic maturation by Furin proprotein-convertase produces the active fragment p61-Sema3E, which is required and sufficient for the function of Sema3E in tumour invasiveness and metastasis (Casazza et al, 2010). Furthermore, Sema3E exerts pleiotropic activities through its specific receptor, Plexin-D1 (PlxnD1), including a collapsing pro-apoptotic response in endothelial cells and a pro-invasive and pro-metastatic effect on tumour cells. This leads to a paradoxical dual effect where the overexpression of Sema3E on one hand reduces the tumour burden by counteracting tumour angiogenesis, but on the other increases the metastatic spread of the tumour. The dual activities of p61-Sema3E depend on the specific transactivated molecules recruited by the complex Sema3E–PlxnD1 in the different types of cells. In endothelial cells, the intrinsic R-Ras GAP activity of PlxnD1 promotes a cell-collapsing response as well as an Arf6 GTPase-mediated integrin-beta1 endocytosis and decreased cellular adhesion to the extracellular matrix (Casazza et al, 2010; Sakurai et al, 2010). In tumour cells, on the contrary, ErbB2 plays a master role in the pro-invasive, pro-metastatic properties of p61-Sema3E with PlxnD1 forming a complex with ErbB2 that results in its transactivation and further activation of EGFR-ErbB2-mediated signalling pathways (Casazza et al, 2010; Fig 1A). Thus, the well-documented negative effect on endothelial cells exerted by Sema3E makes it a good candidate to block angiogenesis in tumours. However, the heightened tumour aggressiveness induced by this pleiotropic molecule precludes its possible exploitation as a therapeutic molecule.


Exploiting pleiotropic activities of semaphorins as multi-target therapies for cancer.

Moserle L, Casanovas O - EMBO Mol Med (2012)

The multi-target effects of p61-Sema3E and uncleavable Sema3E (Uncl-Sema3E) in tumoursEndogenous Sema3E is converted by Furin-mediated cleavage in the active p61-Sema3E. In endothelial cells, its binding to PlxnD1 triggers the intrinsic R-Ras GAP activity of PlxnD1 and results in an anti-angiogenic effect due to the pro-apoptotic collapsing response and disassembly of focal adhesions. In tumour cells, binding of p61-Sema3E to PlxnD1 promotes the formation of a heteromultimeric complex with ErbB2 RTK that leads to its transactivation and further activation of ErbB2-EGFR-mediated pro-invasive and pro-metastatic signalling pathway.Uncl-Sema3E effectively competes with p61-Sema3E for the binding to PlxnD1. Upon binding, it induces PlxnD1 activation and triggers the same signalling molecules and anti-angiogenic effect on endothelial cells. On the contrary, in tumour cells, Uncl-Sema3E binding to PlxnD1 is unable to form a complex and activate the ErbB2-EGFR response, therefore, producing a anti-invasive and anti-metastatic effect.
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Related In: Results  -  Collection

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fig01: The multi-target effects of p61-Sema3E and uncleavable Sema3E (Uncl-Sema3E) in tumoursEndogenous Sema3E is converted by Furin-mediated cleavage in the active p61-Sema3E. In endothelial cells, its binding to PlxnD1 triggers the intrinsic R-Ras GAP activity of PlxnD1 and results in an anti-angiogenic effect due to the pro-apoptotic collapsing response and disassembly of focal adhesions. In tumour cells, binding of p61-Sema3E to PlxnD1 promotes the formation of a heteromultimeric complex with ErbB2 RTK that leads to its transactivation and further activation of ErbB2-EGFR-mediated pro-invasive and pro-metastatic signalling pathway.Uncl-Sema3E effectively competes with p61-Sema3E for the binding to PlxnD1. Upon binding, it induces PlxnD1 activation and triggers the same signalling molecules and anti-angiogenic effect on endothelial cells. On the contrary, in tumour cells, Uncl-Sema3E binding to PlxnD1 is unable to form a complex and activate the ErbB2-EGFR response, therefore, producing a anti-invasive and anti-metastatic effect.
Mentions: Sema3E is one of the SEMAs implicated in tumour invasion and metastatization and its expression correlates with the metastatic process. Sema3E is synthesized as a full-length precursor molecule and its proteolytic maturation by Furin proprotein-convertase produces the active fragment p61-Sema3E, which is required and sufficient for the function of Sema3E in tumour invasiveness and metastasis (Casazza et al, 2010). Furthermore, Sema3E exerts pleiotropic activities through its specific receptor, Plexin-D1 (PlxnD1), including a collapsing pro-apoptotic response in endothelial cells and a pro-invasive and pro-metastatic effect on tumour cells. This leads to a paradoxical dual effect where the overexpression of Sema3E on one hand reduces the tumour burden by counteracting tumour angiogenesis, but on the other increases the metastatic spread of the tumour. The dual activities of p61-Sema3E depend on the specific transactivated molecules recruited by the complex Sema3E–PlxnD1 in the different types of cells. In endothelial cells, the intrinsic R-Ras GAP activity of PlxnD1 promotes a cell-collapsing response as well as an Arf6 GTPase-mediated integrin-beta1 endocytosis and decreased cellular adhesion to the extracellular matrix (Casazza et al, 2010; Sakurai et al, 2010). In tumour cells, on the contrary, ErbB2 plays a master role in the pro-invasive, pro-metastatic properties of p61-Sema3E with PlxnD1 forming a complex with ErbB2 that results in its transactivation and further activation of EGFR-ErbB2-mediated signalling pathways (Casazza et al, 2010; Fig 1A). Thus, the well-documented negative effect on endothelial cells exerted by Sema3E makes it a good candidate to block angiogenesis in tumours. However, the heightened tumour aggressiveness induced by this pleiotropic molecule precludes its possible exploitation as a therapeutic molecule.

View Article: PubMed Central - PubMed

Affiliation: Tumor Angiogenesis Group, Catalan Institute of Oncology - IDIBELL, L'Hospitalet de Llobregat, Spain.

AUTOMATICALLY GENERATED EXCERPT
Please rate it.

See related article in EMBO Molecular Medicine http://dx.doi.org/10.1002/emmm.201100205 Semaphorins (SEMAs) are a superfamily of secreted or membrane-associated glycoproteins implicated in the control of axonal wiring and involved in angiogenesis and cancer progression... The dual activities of p61-Sema3E depend on the specific transactivated molecules recruited by the complex Sema3E–PlxnD1 in the different types of cells... In endothelial cells, the intrinsic R-Ras GAP activity of PlxnD1 promotes a cell-collapsing response as well as an Arf6 GTPase-mediated integrin-beta1 endocytosis and decreased cellular adhesion to the extracellular matrix (Casazza et al, ; Sakurai et al, )... Molecularly, Casazza et al demonstrate that Uncl-Sema3E not only interferes with the endogenous Sema3E signalling, but is also unable to induce the association of PlxnD1 with ErbB2 in the tumour cell context... The study from Casazza et al points out a remarkable pleiotropic anti-cancer potential of Uncl-Sema3E but also reveals several relevant therapeutic opportunities dually targeting angiogenesis and invasion/metastasis. »The study from Casazza et al points out a remarkable pleiotropic anti-cancer potential of Uncl-Sema3E but also reveals several relevant therapeutic opportunities dually targeting angiogenesis and invasion/metastasis. « On the one hand, based on the observation that the uncleavable molecule demonstrates a dominant-negative function over the endogenous Sema3E signalling, one specific therapeutic approach could be the use of a recombinant Uncl-Sema3E as a drug that would maintain the known anti-angiogenic activity of Sema3E without activating the pro-invasive and pro-metastatic process... By inhibiting Furin the endogenous full-length Sema3E would not be effectively cleaved, and an uncleaved form would accumulate in Sema3E-expressing tumours... Uncleaved Sema3E accumulation by Furin inhibition would lead to the competitive blockage of p61-Sema3E pro-invasive and pro-metastatic activity without impairing the anti-angiogenic effects of cleaved Sema3E... To further support this possibility, Furin is frequently expressed in human cancers and its expression correlates with aggressiveness and metastasis, thus making it a potential target for anti-cancer therapies (Christensen et al, )... A crucial point in the putative applicability of Sema3E-related therapies is the critical functional link between Sema3E–PlxnD1 and its transactivated associated molecules... In the context of other anti-tumour therapies, the article from Casazza et al further emphasizes the need of a careful reflection on the use of anti-angiogenic therapy in the treatment of cancer... Due to the implication of different mechanisms involved in the spread of tumour cells promoted by these two distinct treatments, the inhibition of pro-invasive and pro-metastatic process by Uncl-Sema3E strongly supports a possible added therapeutic potential of this molecule in anti-VEGF/R treated tumours... Indeed, results from Casazza et al demonstrate Uncl-Sema3E anti-tumour activity is maintained in models refractory to VEGF therapy... Thus, further efforts have to be made to define the anti-cancer outcome of combinatorial Uncl-Sema3E together with standard anti-angiogenic therapy to determine whether there could be additive anti-angiogenic effects and compensatory anti-invasive and anti-metastatic effects.

Show MeSH
Related in: MedlinePlus