Abstract |
Testicular germ cell tumors (TGCTs) are frequent solid malignant tumors and cause of death in men between 20-40 years of age. Genetic and environmental factors play an important role in the origin and development of TGCTs. Although the majority of TGCTs are responsive to chemotherapy, about 20% of patient presents incomplete response or tumors relapse. In addition, the current treatments cause acute toxicity and several chronic collateral effects, including sterility. The present mini-review collectively summarize the most recent findings on the new discovered molecular biomarkers such as tyrosine kinases, HMGAs, Aurora B kinase, and GPR30 receptor predictive of TGCTs and as emerging new possible molecular targets for therapeutic strategies. J. Cell. Physiol. 232: 276-280, 2017. © 2016 Wiley Periodicals, Inc.
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Authors | Paolo Chieffi |
Journal | Journal of cellular physiology
(J Cell Physiol)
Vol. 232
Issue 2
Pg. 276-280
(Feb 2017)
ISSN: 1097-4652 [Electronic] United States |
PMID | 27405110
(Publication Type: Journal Article, Review)
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Copyright | © 2016 Wiley Periodicals, Inc. |
Chemical References |
- Biomarkers, Tumor
- MicroRNAs
- Protein Kinase Inhibitors
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Topics |
- Biomarkers, Tumor
(metabolism)
- Humans
- Male
- MicroRNAs
(genetics, metabolism)
- Molecular Targeted Therapy
- Neoplasms, Germ Cell and Embryonal
(diagnosis, drug therapy, enzymology, genetics)
- Protein Kinase Inhibitors
(chemistry, therapeutic use)
- Testicular Neoplasms
(diagnosis, drug therapy, enzymology, genetics)
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