Author/Authors :
Shirkavand, Afshan Laser and Plasma Research Institute - Shahid Beheshti University, Tehran, Iran , Mohajerani, Ezeddin Laser and Plasma Research Institute - Shahid Beheshti University, Tehran, Iran , Farivar, Shirin Department of Cell and Molecular Biology - Faculty of Life Sciences and Biotechnology - Shahid Beheshti University, Tehran, Iran , Ataie-Fashtami, Leila Department of Regenerative Medicine - Royan Institute for Stem Cell Biology & Technology, ACECR, Tehran, Iran , Ghazimoradi, Mohammad Hossein Department of Cell and Molecular Biology - Faculty of Life Sciences and Biotechnology - Shahid Beheshti University, Tehran, Iran
Abstract :
Introduction: Skin cancer is one of the most common types of malignancy worldwide. Human
skin naturally contains several endogenous fluorophores, as potential sources can emit inherent
fluorescence, called intrinsic autofluorescence (AF). The melanin endogenous fluorophore in the
basal cell layer of the epidermis seems to have a strong autofluorescence signal among other ones
in the skin. This pilot study aimed to investigate the feasibility of the detection of autofluorescence
signals in the A375 human melanoma cell line in the cell culture stage using the FluoVision optical
imaging system.
Methods: The human skin melanoma cell line (A375) donated as a gift from Switzerland (University
Hospital Basel) was cultured. For the imaging of the A375 human melanoma cell sample in this
pilot study, the FluoVision optical imaging device (Tajhiz Afarinan Noori Parseh Co) was applied.
The proposed clustering image processing code was developed based on the K-mean segmentation
method, using MATLAB software (version 16).
Results: The quantification of color pixels in the color bar along with the intensity score of the
autofluorescence signal ranged between 0 and 70 was written in the image processing code
execution and a threshold higher than 40%, proportional to the ratio of autofluorescent cells. The
percentage of the signal of A375 autofluorescent melanoma cells in the 3 studied cell samples was
calculated as 3.11%±0.6.
Conclusion: This imaging method has the advantage of no need for fluorophore labels over the
existing fluorescence imaging methods, and it can be regarded as one of the important choices of
label-free imaging for this A375 melanoma cell line containing the intrinsic endogenous fluorophore
in cell studies.
Keywords :
Human Melanoma A375 , Autofluorescence imaging , Segmentation , Quantitative , Image Processing