Testicular and Haematological Cancer Induce Very High Levels of Sperm Oxidative Stress

Cancer impairs spermatogenesis, whereas results on sperm DNA integrity are controversial and no data are available about sperm oxidative stress. In cancer patients, we detected sperm DNA fragmentation (sDF) and both viable (ROS production in viable sperm fraction/viable spermatozoa) and total (ROS p...

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Main Authors: Costanza Calamai (Author), Oumaima Ammar (Author), Viktoria Rosta (Author), Ginevra Farnetani (Author), Salvatore Zimmitti (Author), Lisa Giovannelli (Author), Linda Vignozzi (Author), Csilla Krausz (Author), Monica Muratori (Author)
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Published: MDPI AG, 2023-05-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Costanza Calamai  |e author 
700 1 0 |a Oumaima Ammar  |e author 
700 1 0 |a Viktoria Rosta  |e author 
700 1 0 |a Ginevra Farnetani  |e author 
700 1 0 |a Salvatore Zimmitti  |e author 
700 1 0 |a Lisa Giovannelli  |e author 
700 1 0 |a Linda Vignozzi  |e author 
700 1 0 |a Csilla Krausz  |e author 
700 1 0 |a Monica Muratori  |e author 
245 0 0 |a Testicular and Haematological Cancer Induce Very High Levels of Sperm Oxidative Stress 
260 |b MDPI AG,   |c 2023-05-01T00:00:00Z. 
500 |a 10.3390/antiox12061145 
500 |a 2076-3921 
520 |a Cancer impairs spermatogenesis, whereas results on sperm DNA integrity are controversial and no data are available about sperm oxidative stress. In cancer patients, we detected sperm DNA fragmentation (sDF) and both viable (ROS production in viable sperm fraction/viable spermatozoa) and total (ROS production in viable sperm fraction/total spermatozoa) oxidative stress. We found that cancer (22.50 (17.00-26.75)%, <i>n</i> = 85) increased sDF with respect to the control groups in both normozoospermic subfertile patients (NSP) (12.75 (8.63-14.88)%, <i>n</i> = 52, <i>p</i> < 0.001) and in healthy donors (HD) (8.50 (7.00-14.00)%, <i>n</i> = 19, <i>p</i> < 0.001). The induction of viable oxidative stress (<i>n</i> = 96) with cancer was even higher: 36.60 (24.05-58.65)% versus 11.10 (8.63-14.90)% in NSP (<i>p</i> < 0.001) and 9.60 (8.00-14.03)% in HD (<i>p</i> < 0.001). Similar, albeit lower, differences were found for total oxidative stress. SDF sharply correlated to viable oxidative stress when we considered all subjects (cancer patients and controls) (r = 0.591, <i>p</i> < 0.001, <i>n</i> = 134), but no correlation was found when only cancer patients were studied (r = 0.200; <i>p</i> > 0.05, <i>n</i> = 63). In conclusion, cancer significantly increases sDF and sperm oxidative stress levels. Additional mechanisms to oxidative attack might be responsible for increased sDF in cancer patients. Because sperm oxidative stress might affect the outcomes of sperm cryopreservation, of cancer treatments and of sperm epigenoma, the detection of oxidative stress could be of help in managing the reproductive issues of cancer patients. 
546 |a EN 
690 |a sperm oxidative stress 
690 |a sperm DNA fragmentation 
690 |a cancer 
690 |a seminoma 
690 |a non-seminoma 
690 |a orchiectomy 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Antioxidants, Vol 12, Iss 6, p 1145 (2023) 
787 0 |n https://www.mdpi.com/2076-3921/12/6/1145 
787 0 |n https://doaj.org/toc/2076-3921 
856 4 1 |u https://doaj.org/article/e20c46bae7ac46e9a95461e0353058d6  |z Connect to this object online.