Induction of apoptotic cell death in non-melanoma skin cancer by interferon-α

1995 ◽  
Vol 61 (1) ◽  
pp. 110-114 ◽  
Author(s):  
Julio Rodríguez-Villanueva ◽  
Timothy J. McDonnell
RSC Advances ◽  
2016 ◽  
Vol 6 (85) ◽  
pp. 82205-82218 ◽  
Author(s):  
J. Grace Nirmala ◽  
S. Akila ◽  
M. S. A. Muthukumar Nadar ◽  
R. T. Narendhirakannan ◽  
Suvro Chatterjee

Cytotoxic and apoptotic effects of Vitis vinifera seed gold nanoparticles on A431 cell lines.


Biomedicines ◽  
2021 ◽  
Vol 9 (6) ◽  
pp. 597
Author(s):  
Barbara Bellei ◽  
Silvia Caputo ◽  
Emilia Migliano ◽  
Gianluca Lopez ◽  
Valeria Marcaccini ◽  
...  

Background: Cancer-associated fibroblasts (CAFs) facilitate many aspects of cancer development by providing a structural framework rich in bioactive compounds. There are emerging studies proposing a combination of conventional anti-cancer therapies directed against neoplastic cells to molecules targeting tumor microenvironments. Methods: The study evaluated the pharmacological properties of the anti-tumor agent paclitaxel conjugated to hyaluronic acid (HA) regarding non-melanoma skin cancer (NMSC) and the surrounding fibroblasts. This molecule, named Oncofid-P20 (Onco-P20), preferentially targets cells expressing high levels of CD44, the natural ligand of HA. Results: Consistent with paclitaxel’s mechanism of action involving interference with the breakdown of microtubules during cell division, highly sensitive carcinoma cells rapidly underwent apoptotic cell death. Interestingly, less sensitive cells, such as dermal fibroblasts, resisted the Onco-P20 treatment and experienced a prolonged growth arrest characterized by morphological change and significant modification of the gene expression profile. Onco-P20-treated fibroblasts exhibited reduced growth factor production, downmodulation of the Wnt signaling pathway, and the acquisition of a marked pro-inflammatory profile. Independently of direct exposure to taxol, in the presence of Onco-P20-treated fibroblasts or in their conditioned medium, carcinoma cells had a reduced proliferation rate. Similar to NHF, fibroblasts isolated from skin cancer lesions or from adjacent tissue acquired anti-neoplastic activity under Onco-P20 treatment. Conclusion: Collectively, our data demonstrate that Onco-P20, exerting both a direct and an NHF-mediated indirect effect on carcinoma cells, is a candidate for an innovative therapy alternative to surgery for the treatment of NMSC.


2020 ◽  
Vol 140 (7) ◽  
pp. S82
Author(s):  
T.R. Holmes ◽  
J. Al-Matouq ◽  
M. Holmes ◽  
N. Sioda ◽  
J. Rudd ◽  
...  

2020 ◽  
Author(s):  
Barbara Bellei ◽  
Silvia Caputo ◽  
Emilia Migliano ◽  
Gianluca Lopez ◽  
Valeria Marcaccini ◽  
...  

Abstract Background: Cancers are complex organs which encompass not only the tumor cells but also cells within the surrounding stroma. Such cells, mainly cancer associated fibroblasts (CAFs) and immune infiltrating cells, facilitate many aspects of cancer development providing a structural and supportive framework rich of bioactive compounds. So far, there are emerging studies proposing the combination of conventional anti-cancer therapy, directed against neoplastic cells, to molecules targeting tumor microenviroment.Methods: The study was designed to evaluated the pharmacological properties of the anti-tumor agent paclitaxel conjugated to hyaluronic acid (HA) on non-melanoma skin cancer (NMSC) and on the surronding dermal fibroblasts. This molecule, named Oncofid-P20 (Onco-P20), targets preferentially cells expressing high level of CD44, the natural ligand of HA.Results: Consistent with paclitaxel’s mechanism of action involving interferences with the normal breackdown of microtubules during cell division, highly sensible carcinoma cells underwent rapidly to apoptotic cell death. Interestingly, less sensible cells such as dermal fibroblasts resisted to the Onco-P20 treatment and experirenced a prologed growth arrest characterized by morphological change and significant modification of the gene espression profile that partially overlaps with that of senescent cells. Onco-P20-treated fibroblasts lowered growth factors production, down-modulate Wnt signal pathway and acquired a marked pro-inflammatory profile. Independently to the direct exposure to taxol, in presence of Onco-P20-treated fibroblasts or their conditioned medium, carcinoma cells reduced the proliferation rate. Similar to NHF, fibroblasts isolated from skin cancer tumor lesion or from tissue adjacent to the tumor acquired an anti-neoplastic activity under Oncofid-P20 treatment.Conclusion: Collectively, our data demonstrated that Onco-P20, exerting both a direct and a NHF-mediated indirect paracrine effect on carcinoma cells, is a good candidate for an innovative therapy alternative to surgery for treatment of NMSC.


2017 ◽  
Vol 70 (2) ◽  
pp. 537-554 ◽  
Author(s):  
J. Grace Nirmala ◽  
S. Evangeline Celsia ◽  
Akila Swaminathan ◽  
R. T. Narendhirakannan ◽  
Suvro Chatterjee

1994 ◽  
Vol 86 (1) ◽  
pp. 169-173 ◽  
Author(s):  
Panayiotis Panayiotidis ◽  
Kanagasabai Ganeshaguru ◽  
Shireen Aafa ◽  
B. Jabbar ◽  
A. Victor Hoffbrand

Oncotarget ◽  
2020 ◽  
Vol 11 (35) ◽  
pp. 3267-3278
Author(s):  
Thomas R. Holmes ◽  
Jenan Al-Matouq ◽  
Matti Holmes ◽  
Lauren Nicola ◽  
Justin C. Rudd ◽  
...  

2020 ◽  
Author(s):  
Barbara Bellei ◽  
Silvia Caputo ◽  
Emilia Migliano ◽  
Gianluca Lopez ◽  
Valeria Marcaccini ◽  
...  

Abstract Background: Cancers are complex organs which encompass not only the tumor cells but also cells within the surrounding stroma. Such cells, mainly cancer associated fibroblasts (CAFs) and immune infiltrating cells, facilitate many aspects of cancer development providing a structural and supportive framework rich of bioactive compounds. So far, there are emerging studies proposing the combination of conventional anti-cancer therapy, directed against neoplastic cells, to molecules targeting tumor microenviroment. Methods: The study was designed to evaluated the pharmacological properties of the anti-tumor agent paclitaxel conjugated to hyaluronic acid (HA) on non-melanoma skin cancer (NMSC) and on the surronding dermal fibroblasts. This molecule, named Oncofid-P20 (Onco-P20), targets preferentially cells expressing high level of CD44, the natural ligand of HA.Results: Consistent with paclitaxel’s mechanism of action involving interferences with the normal breackdown of microtubules during cell division, highly sensible carcinoma cells underwent rapidly to apoptotic cell death. Interestingly, less sensible cells such as dermal fibroblasts resisted to the Onco-P20 treatment and experirenced a senescent-like status characterized by morphological change, decreaded proliferation, and significant modification of the gene espression profile. Onco-P20-treated fibroblasts lowered growth factors production, down-modulate Wnt signal pathway and acquired a pro-inflammatory profile. Independently to the direct exposure to taxol, in presence of Onco-P20-treated fibroblasts or their conditioned medium, carcinoma cells reduced the proliferation rate. Similar to NHF, fibroblasts isolated from skin cancer tumor lesion or from tissue adjacent to the tumor acquired an anti-neoplastic activity under Oncofid-P20 treatment.Conclusion: Collectively, our data demonstrated that Onco-P20, exerting both a direct and a NHF-mediated indirect paracrine effect on carcinoma cells, is a good candidate for an innovative therapy alternative to surgery for treatment of NMSC.


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