scholarly journals Can antioxidants protect against chemotherapy in rat spermatogonial stem cell line?

Author(s):  
Caroline M Allen ◽  
Federica Lopes ◽  
Rod T Mitchell ◽  
Norah Spears

LAY ABSTRACT: Boys administered chemotherapy to treat childhood cancer are at risk of damage to their healthy testicular tissue, which can lead to infertility in adulthood. Researchers are therefore investigating treatments to protect the testis during cancer treatment. Here, cells originating from the testicles of rats were cultured for four days and exposed to chemotherapy drugs with or without antioxidants for the final two days. Antioxidants can reduce cellular damage by inactivating toxic compounds. Here, the antioxidants melatonin or n-acetylcysteine were tested against chemotherapy agents’ cisplatin, doxorubicin, or vincristine. Cultures were repeated four times, with cell survival measured at the end of culture. The antioxidants themselves were not damaging to the cells and partially protected against cisplatin, although not against doxorubicin. Surprisingly, n-acetylcysteine was found to enhance the damage induced by vincristine. The results suggest that using antioxidants to try to protect the testis could have either beneficial or harmful effects when given alongside different chemotherapy drugs: this is important, considering that patients are often treated with multiple drugs which could react differently to protectants.

2010 ◽  
Vol 83 (5) ◽  
pp. 742-749 ◽  
Author(s):  
Gianfranco Carlomagno ◽  
Maaike P.A. van Bragt ◽  
Cindy M. Korver ◽  
Sjoerd Repping ◽  
Dirk G. de Rooij ◽  
...  

2014 ◽  
Vol 17 (5) ◽  
pp. 211-216 ◽  
Author(s):  
Jeong Hyun Kim ◽  
Neelesh Sharma ◽  
Sung Woo Kim ◽  
Simrinder Singh Sodhi ◽  
Mrinmoy Ghosh ◽  
...  

2013 ◽  
Vol 114 (4) ◽  
pp. 920-928 ◽  
Author(s):  
Haesun Youn ◽  
Song-Hee Kim ◽  
Kyung Ah Choi ◽  
Sungtae Kim

2013 ◽  
Vol 66 (3) ◽  
pp. 365-372 ◽  
Author(s):  
Peng Wang ◽  
Li-Juan Suo ◽  
Hua Shang ◽  
Ying Li ◽  
Guang-Xuan Li ◽  
...  

2018 ◽  
Vol 120 (1) ◽  
pp. 613-621 ◽  
Author(s):  
Seyedeh‐Faezeh Moraveji ◽  
Fereshteh Esfandiari ◽  
Mina Sharbatoghli ◽  
Sara Taleahmad ◽  
Saman Nikeghbalian ◽  
...  

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Jia Tian ◽  
Ke Ma ◽  
Cheng-bin Pei ◽  
Shao-hua Zhang ◽  
Xue Li ◽  
...  

Abstract Background Spermatogonial stem cell (SSC) transplantation technology as a promising option for male fertility preservation has received increasing attention, along with efficient SSC purification technology as a necessary technical support; however, the safety of such application in patients with tumors remains controversial. Methods In this study, we used a green fluorescent protein mouse xenograft model of B cell acute lymphocytic leukemia. We isolated and purified SSCs from the testicular tissue of model mice using density gradient centrifugation, immune cell magnetic bead separation, and flow cytometry. The purified SSCs were transplanted into convoluted seminiferous tubules of the nude mice and C57BL/6 male mice subjected to busulfan. The development and proliferation of SSCs in the recipient testis were periodically tested, along with whether B cell acute lymphocytic leukemia was induced following SSC implantation. The genetic characteristics of the offspring obtained from natural mating were also observed. Results In testicular leukemia model mice, a large number of BALL cells infiltrated into the seminiferous tubule, spermatogenic cells, and sperm cells in the testis tissue decreased. After spermatogonial stem cell transplantation, the transplanted SSCs purified by immunomagnetic beads and flow cytometry methods colonized and proliferated extensively in the basement of the seminiferous tubules of mice; a large number of spermatogenic cells and sperm were found in recipient testicular tissue after 12 weeks of SSC transplantation. In leukemia detection in nude mice after transplantation in the three SSC purification groups, a large number of BALL cells could be detected in the blood of recipient mice 2–3 weeks after transplantation in the density gradient centrifugation group, but not in the blood of the flow cytometry sorting group and the immunomagnetic bead group after 16 weeks of observation. Conclusions In this study, we confirmed that immunomagnetic beads and flow cytometry methods of purifying SSCs from the testicular tissue of the testicular leukemia mouse model could be safely applied to the SSC transplantation technology without concomitant tumor implantation. The results thus provide a theoretical basis for the application of tumor SSC cryopreservation for fertility preservation in patients with tumors.


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