Abstract B42: An investigation into the synergistic action of chemotherapy and photodynamic therapy (PDT) in resistant human melanoma

Author(s):  
Fleury Augustin Nsole-Biteghe ◽  
Olawale Ajuwon ◽  
Lester M. Davids
2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Khatereh Khorsandi ◽  
Reza Hosseinzadeh ◽  
Elham Chamani

Abstract Background Melanoma as a type of skin cancer, is associated with a high mortality rate. Therefore, early diagnosis and efficient surgical treatment of this disease is very important. Photodynamic therapy (PDT) involves the activation of a photosensitizer by light at specific wavelength that interacts with oxygen and creates singlet oxygen molecules or reactive oxygen species (ROS), which can lead to tumor cell death. Furthermore, one of the main approches in the prevention and treatment of various cancers is plant compounds application. Phenolic compounds are essential class of natural antioxidants, which play crucial biological roles such as anticancer effects. It was previously suggested that flavonoid such as rutoside could acts as pro-oxidant or antioxidant. Hence, in this study, we aimed to investigate the effect of rutoside on the combination therapy with methylene blue (MB) assisted by photodynamic treatment (PDT) using red light source (660 nm; power density: 30 mW/cm2) on A375 human melanoma cancer cells. Methods For this purpose, the A375 human melanoma cancer cell lines were treated by MB-PDT and rutoside. Clonogenic cell survival, MTT assay, and cell death mechanisms were also determined after performing the treatment. Subsequently, after the rutoside treatment and photodynamic therapy (PDT), cell cycle and intracellular reactive oxygen species (ROS) generation were measured. Results The obtained results showed that, MB-PDT and rutoside had better cytotoxic and antiprolifrative effects on A375 melanoma cancer cells compared to each free drug, whereas the cytotoxic effect on HDF human dermal fibroblast cell was not significant. MB-PDT and rutoside combination induced apoptosis and cell cycle arrest in the human melanoma cancer cell line. Intracellular ROS increased in A375 cancer cell line after the treatment with MB-PDT and rutoside. Conclusion The results suggest that, MB-PDT and rutoside could be considered as novel approaches as the combination treatment of melanoma cancer.


2009 ◽  
Vol 6 (2) ◽  
pp. 105-116 ◽  
Author(s):  
Abdel-Megid Mamoon ◽  
Amira M. Gamal–Eldeen ◽  
Meghan E. Ruppel ◽  
Randy J. Smith ◽  
Thomas Tsang ◽  
...  

2015 ◽  
Vol 24 (12) ◽  
pp. 970-972 ◽  
Author(s):  
Paula A. Barbugli ◽  
Cleidson P. Alves ◽  
Enilza M. Espreafico ◽  
Antonio C. Tedesco

2007 ◽  
Vol 4 (7) ◽  
pp. 546-551 ◽  
Author(s):  
P F C Menezes ◽  
V S Bagnato ◽  
R M Johnke ◽  
C Bonnerup ◽  
C H Sibata ◽  
...  

2001 ◽  
Vol 48 (1) ◽  
pp. 277-282 ◽  
Author(s):  
A Drzewiecka ◽  
K Urbańska ◽  
Z Matuszak ◽  
M Pineiro ◽  
L G Arnaut ◽  
...  

We report the synthesis, photochemical and photophysical properties and preliminary studies on biological effect of a new tritolylporphyrin dimer (T-D). Absorption and emission properties of T-D suggest its possible use in photodynamic therapy. T-D is capable of singlet oxygen production with 0.8 quantum yield. It also has a high photostability. The photodynamic properties of the dimer were examined following the growth of SKMEL 188 (human melanoma) cells irradiated with red light (cut off < 630 nm). The surviving fraction of the cells decreased about 3-fold (vs. non-irradiated cells) for an 81 J/cm dose. Our results suggest that tritolylporphyrine dimer T-D may be an interesting hydrophobic sensitizer for photodynamic therapy.


2016 ◽  
Vol 13 ◽  
pp. 297-302 ◽  
Author(s):  
Hadis Tahmasebi ◽  
Karim Khoshgard ◽  
Ameneh Sazgarnia ◽  
Ali Mostafaie ◽  
Mohammad Taghi Eivazi

2010 ◽  
Vol 99 (2) ◽  
pp. 100-104 ◽  
Author(s):  
Sirinart Chio-Srichan ◽  
Noufissa Oudrhiri ◽  
Annelise Bennaceur-Griscelli ◽  
Ali G. Turhan ◽  
Paul Dumas ◽  
...  

Author(s):  
James R. Gaylor ◽  
Fredda Schafer ◽  
Robert E. Nordquist

Several theories on the origin of the melanosome exist. These include the Golgi origin theory, in which a tyrosinase-rich protein is "packaged" by the Golgi apparatus, thus forming the early form of the melanosome. A second theory postulates a mitochondrial origin of melanosomes. Its author contends that the melanosome is a modified mitochondria which acquires melanin during its development. A third theory states that a pre-melanosome is formed in the smooth or rough endoplasmic reticulum. Protein aggregation is suggested by one author as a possible source of the melanosome. This fourth theory postulates that the melanosome originates when the protein products of several genetic loci aggregate in the cytoplasm of the melanocyte. It is this protein matrix on which the melanin is deposited. It was with these theories in mind that this project was undertaken.


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