Testicular Cancer

Author(s):  
Lorenzo Richiardi ◽  
Giovenale Moirano ◽  
Pagona Lagiou

Testicular cancer is highly curable and, though relatively rare, it is the most common cancer among young men. Incidence of testicular cancer has been increasing constantly around the world since the beginning of the twentieth century, but factors responsible for the rise in incidence remain enigmatic. Only few risk factors for testicular cancer are established, including age, ethnic group, cryptorchidism and hypospadias, contralateral testicular cancer, family history, and height. While analytic epidemiologic research has provided numerous etiologic clues, many of them remain tentative. Overwhelming evidence indicates the fundamental importance of environmental factors in the etiology of this enigmatic cancer. Prenatal exposures seem to be instrumental in shaping the risk of testicular cancer, but postnatal exposures acting in childhood, adolescence, and very early adulthood are also important. Testicular cancer has also a strong genetic component that is studied through international collaborations and genome-wide association studies.

2020 ◽  
Vol 25 (40) ◽  
pp. 4274-4286 ◽  
Author(s):  
Huilei Zheng ◽  
Zhiyu Zeng ◽  
Hong Wen ◽  
Peng Wang ◽  
Chunxia Huang ◽  
...  

Coronary artery disease (CAD) is a complex disease caused by the combination of environmental and genetic factors. It is one of the leading causes of death and disability in the world. Much research has been focussed on CAD genetic mechanism. In recent years, genome-wide association study (GWAS) has developed rapidly around the world. Medical researchers around the world have successfully discovered a series of CAD genetic susceptibility genes or susceptible loci using medical research strategies, leading CAD research toward a new stage. This paper briefly summarizes the important progress made by GWAS for CAD in the world in recent years, and then analyzes the challenges faced by GWAS at this stage and the development trend of future research, to promote the transformation of genetic research results into clinical practice and provide guidance for further exploration of the genetic mechanism of CAD.


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