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Assessment of extracorporeal photopheresis related cell damage.
Samur, Bahadir M; Karakukcu, Cigdem; Ozcan, Alper; Unal, Ekrem; Yilmaz, Ebru; Karakukcu, Musa.
Afiliação
  • Samur BM; Department of Pediatrics, Erciyes University, Faculty of Medicine, Kayseri, Turkey. Electronic address: mbahadirsamur@yahoo.com.
  • Karakukcu C; Department of Biochemistry, Erciyes University, Faculty of Medicine, Kayseri, Turkey; Drug Application and Research Center, Erciyes University, Kayseri, Turkey. Electronic address: ckarakukcu@erciyes.edu.tr.
  • Ozcan A; Department of Pediatrics, Division of Pediatric Hematology Oncology, Erciyes University Faculty of Medicine, KANKA Pediatric Hematology & Oncolgy Hospital, Kayseri, Turkey. Electronic address: dralperozcan@hotmail.com.
  • Unal E; Department of Pediatrics, Division of Pediatric Hematology Oncology, Erciyes University Faculty of Medicine, KANKA Pediatric Hematology & Oncolgy Hospital, Kayseri, Turkey; Erciyes University, Department of Molecular Biology and Genetics, Gevher Nesibe Genome and Stem Cell Institution, Genome an
  • Yilmaz E; Department of Pediatrics, Division of Pediatric Hematology Oncology, Bone Marrow Transplantation Center, Erciyes University Faculty of Medicine, KANKA Pediatric Hematology & Oncolgy Hospital, Kayseri, Turkey. Electronic address: drebruyilmaz01@yahoo.com.tr.
  • Karakukcu M; Department of Pediatrics, Division of Pediatric Hematology Oncology, Bone Marrow Transplantation Center, Erciyes University Faculty of Medicine, KANKA Pediatric Hematology & Oncolgy Hospital, Kayseri, Turkey. Electronic address: mkkukcu@yahoo.com.
Transfus Apher Sci ; 61(6): 103472, 2022 Dec.
Article em En | MEDLINE | ID: mdl-35637126
ABSTRACT

AIM:

Extracorporeal photochemotherapy (ECP) is emphasized chiefly as it has a high safety profile. However, the genotoxic effects of ECP are not known. This experimental study aimed to assess the potential genotoxic impact of ECP treatment by the AKLIDES system, a new generation standardized and automated evaluation method. MATERIALS AND

METHODS:

Buffy coats were obtained from the blood of 26 healthy volunteers, and ECP was applied to 2 j/cm2 UV-A for two hours. After the DNA isolation procedure, all slides were stained with DAPI to visualize lymphocytes, FITC for visualization of damage foci marker (γH2AX), and APC for visualization of repair foci marker (53BP1). With the AKLIDES imaging system, all parameters were evaluated.

RESULTS:

Median damage marker Foci γ-H2AX before and after ECP were 11.42 and 18.65 arbitrary units, respectively (p = 0.153). Median repair marker foci 53BP1 (repair biomarker) before and after ECP were measured as 4.17 and 6.7 arbitrary units. The difference was also not statistically significant (p = 0.088). Although 58 % of cells were affected by ECP irradiation, as shown by FITC fluorescent staining, no statistical difference was found in any genotoxicity parameters.

CONCLUSION:

We found an increase in the foci γ-H2AX parameter, one of the objective indicators of DNA breaks, and an increase in the foci 53BP1 parameter, which indicates the post-damage repair mechanisms after ECP. However, further in vitro, and in vivo studies are needed with large sample volumes to demonstrate the significance.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fotoferese Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fotoferese Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article