Radiation sensitivity of human squamous cell carcinoma cells in vitro is modulated by all-trans and 13-cis-retinoic acid in combination with interferon-α

Author(s):  
Wolfgang Hoffmann ◽  
Marcel A. Bläse ◽  
Lan Santo-Hoeltje ◽  
Carsten Herskind ◽  
Michael Bamberg ◽  
...  
1999 ◽  
Vol 175 (11) ◽  
pp. 563-568 ◽  
Author(s):  
Marcel Bläse ◽  
Marco-Michael Zaruba ◽  
Lan Santo-Hoeltje ◽  
Michael Bamberg ◽  
Wolfgang Hoffmann ◽  
...  

1990 ◽  
Vol 123 (1) ◽  
pp. 1 ◽  
Author(s):  
Jeffery L. Schwartz ◽  
Reba Mustafi ◽  
Michael A. Beckett ◽  
Ralph R. Weichselbaum

Molecules ◽  
2019 ◽  
Vol 24 (9) ◽  
pp. 1793 ◽  
Author(s):  
Silvia Tampucci ◽  
Sara Carpi ◽  
Maria Digiacomo ◽  
Beatrice Polini ◽  
Stefano Fogli ◽  
...  

In this work, hybrid compounds 1–4 obtained by conjugation of the non-steroidal anti-inflammatory drug diclofenac, with natural molecules endowed with antioxidant and antiproliferative activity were prepared. The antiproliferative activity of these hybrids was evaluated on immortalized human keratinocyte (HaCaT) cells stimulated with epidermal growth factor (EGF), an actinic keratosis (AK) model, and on human squamous cell carcinoma (SCC) cells (A431). Hybrid 1 presented the best activity in both cell models. Self-assembling surfactant nanomicelles have been chosen as the carrier to drive the hybrid 1 into the skin; the in vitro permeation through and penetration into pig ear skin have been evaluated. Among the nanostructured formulations tested, Nano3Hybrid20 showed a higher tendency of the hybrid 1 to be retained in the skin rather than permeating it, with a desirable topical and non-systemic action. On these bases, hybrid 1 may represent an attractive lead scaffold for the development of new treatments for AK and SCC.


2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Xiaofeng Qi ◽  
Wengguang Xu ◽  
Junqi Xie ◽  
Yufeng Wang ◽  
Shengwei Han ◽  
...  

Abstract Resistance towards chemotherapy is a common complication in treatment of oral cancers, which leads to treatment failure and poor outcome. In recent years, a growing body of evidence has shown that tumour hypoxia significantly contributes to chemoresistance. Metformin, a widely used oral hypoglycaemic drug, can reportedly potentiate the efficacy of chemotherapeutic drugs in various cancers; however, the underlying mechanisms are intricate and have not been fully understood. In this study, we explored the role of metformin in chemosensitivity of oral squamous cell carcinoma cells (OSCC) to cisplatin both in vitro and in vivo, and attempted to elucidate its possible underlying mechanisms. Encouragingly, we found that metformin synergistically enhanced cisplatin cytotoxicity and reversed the chemoresistance to certain extent. This mechanism could likely be related with inhibition of the NF-κB/HIF-1α signal axis and lead to the downregulation of hypoxia-regulated genes products. Therefore, metformin could serve as a chemosensitiser for cisplatin-based regimens for OSCC, thereby providing a theoretical basis for future use in the treatment of oral cancers.


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