Testosterone regulation on quiescin sulfhydryl oxidase 2 synthesis in the epididymis

Reproduction ◽  
2021 ◽  
Author(s):  
Tse-en Wang ◽  
Shiori Minabe ◽  
Fuko Matsuda ◽  
Sheng-Hsiang Li ◽  
Hiroko Tsukamura ◽  
...  

The epididymis is an androgen-responsive organ, whose structure and functions are modulated by the coordination between androgen and epididymal cues. Highly-regulated molecular interaction within the epididymis is required to support viable sperm development necessary for subsequent fertilization. In the present study, we extended our earlier findings on a promising epididymal protein, quiescin sulfhydryl oxidase 2 (QSOX2), and demonstrated a positive correlation between testosterone and QSOX2 protein synthesis through use of loss- and restore-of-function animal models. Moreover, based on transcriptomic analyses and 2-dimensional culture system, we determined that an additional polarized effect of glutamate is indispensable for the regulatory action of testosterone on QSOX2 synthesis. In conclusion, we propose non-canonical testosterone signaling supports epididymal QSOX2 protein synthesis, providing a novel perspective on the regulation of sperm maturation within the epididymis.

2018 ◽  
Vol 19 (10) ◽  
pp. 3213 ◽  
Author(s):  
Hye-Jin Sung ◽  
Jung-Mo Ahn ◽  
Yeon-Hee Yoon ◽  
Sang-Su Na ◽  
Young-Jin Choi ◽  
...  

As lung cancer shows the highest mortality in cancer-related death, serum biomarkers are demanded for lung cancer diagnosis and its treatment. To discover lung cancer protein biomarkers, secreted proteins from primary cultured lung cancer and adjacent normal tissues from patients were subjected to LC/MS–MS proteomic analysis. Quiescin sulfhydryl oxidase (QSOX1) was selected as a biomarker candidate from the enriched proteins in the secretion of lung cancer cells. QSOX1 levels were higher in 82% (51 of 62 tissues) of lung cancer tissues compared to adjacent normal tissues. Importantly, QSOX1 serum levels were significantly higher in cancer patients (p < 0.05, Area Under curve (AUC) = 0.89) when measured by multiple reaction monitoring (MRM). Higher levels of QSOX1 were also uniquely detected in lung cancer tissues, among several other solid cancers, by immunohistochemistry. QSOX1-knock-downed Lewis lung cancer (LLC) cells were less viable from oxidative stress and reduced migration and invasion. In addition, LLC mouse models with QSOX1 knock-down also proved that QSOX1 functions in promoting cancer metastasis. In conclusion, QSOX1 might be a lung cancer tissue-derived biomarker and be involved in the promotion of lung cancers, and thus can be a therapeutic target for lung cancers.


PLoS ONE ◽  
2013 ◽  
Vol 8 (1) ◽  
pp. e55621 ◽  
Author(s):  
Wael Gad ◽  
Meera G. Nair ◽  
Karolien Van Belle ◽  
Khadija Wahni ◽  
Henri De Greve ◽  
...  

2020 ◽  
Vol 333 ◽  
pp. 127492
Author(s):  
Nian Du ◽  
Zhen-Cheng Wei ◽  
Yuan-Yuan Deng ◽  
Yan Zhang ◽  
Xiao-Jun Tang ◽  
...  

FEBS Letters ◽  
2012 ◽  
Vol 586 (23) ◽  
pp. 4119-4125 ◽  
Author(s):  
Keren Limor-Waisberg ◽  
Assaf Alon ◽  
Tevie Mehlman ◽  
Deborah Fass

Biochemistry ◽  
2012 ◽  
Vol 51 (20) ◽  
pp. 4226-4235 ◽  
Author(s):  
Jennifer A. Codding ◽  
Benjamin A. Israel ◽  
Colin Thorpe

2013 ◽  
Vol 13 (1) ◽  
pp. 70 ◽  
Author(s):  
Keren Limor-Waisberg ◽  
Shifra Ben-Dor ◽  
Deborah Fass

1990 ◽  
Vol 161 (1) ◽  
pp. 43-47
Author(s):  
HIDEAKI KONG ◽  
YOUNG CHIN LIN ◽  
MAMORU YAMAGUCHI ◽  
ATSUSHI SANBUISSHO ◽  
FREDERICK P. ZUSPAN ◽  
...  

2007 ◽  
Vol 26 (13) ◽  
pp. 3203-3215 ◽  
Author(s):  
Santiago Alejandro ◽  
Pedro L Rodríguez ◽  
Jose M Bellés ◽  
Lynne Yenush ◽  
María J García-Sanchez ◽  
...  

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