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mTOR expression in human testicular seminoma
A Yaba1, E R Bozkurt2, N Demir3
1Institute of Health Sciences, Yeditepe University, İstanbul, Turkey.
Abstract:
The mammalian target of rapamycin (TOR) has been implicated in the control of different stressors, growth factors, nutrients and hormones, participating in the control of key cellular functions. Controlling this many pathways poses mTOR signalling as a potential new target in new treatment strategies for multiple cancer types. mTOR components could potentially mislocated in tumour cells, which could lead to activation of signalling pathway that should not be active. Therefore, we aimed to show localisation of mTOR signal proteins in testicular seminoma. Tumoural testicular tissues were obtained from 10 patients with unilateral classic seminoma undergoing to therapeutic orchidectomy and compared with control human testicular tissues. Upon immunohistochemical evaluation, we detected mTOR and p-mTOR (serine 2448), P70S6K, p-P70S6K, PKCalpha and p-PKCalpha, CD36 and MAPLC3 proteins in the cytoplasm of Sertoli cells in the seminiferous tubules. We also showed cytoplasmic perinuclear staining in seminoma cells. This study demonstrated the interaction of mTOR signalling pathway and testicular seminoma by showing intense cytoplasmic mTOR pathway proteins immunoreactivity in the seminoma, for the first time in humans. Therefore, we suggested that mTOR signalling components could create new clinical targets for treatment of testicular seminoma patients and male infertility in the future.
Insights
The mammalian target of rapamycin (mTOR) pathway proteins are found in testicular seminoma cells. This suggests mTOR signaling could be a new therapeutic target for testicular cancer and male infertility.
Area of Science:
- Oncology
- Cell Biology
- Molecular Signaling
Background:
- The mammalian target of rapamycin (mTOR) pathway regulates crucial cellular functions in response to various stimuli.
- Dysregulation of mTOR signaling is implicated in multiple cancer types, making it a promising therapeutic target.
- Aberrant localization of mTOR components in tumor cells may lead to uncontrolled pathway activation.
Purpose of the Study:
- To investigate the localization of key mTOR signaling pathway proteins in human testicular seminoma.
- To determine if mTOR pathway components are mislocalized in seminoma cells compared to normal testicular tissue.
Main Methods:
- Immunohistochemical analysis of tumor and control human testicular tissues from 10 seminoma patients.
- Detection of mTOR, p-mTOR (serine 2448), P70S6K, p-P70S6K, PKCalpha, p-PKCalpha, CD36, and MAPLC3 proteins.
Main Results:
- mTOR pathway proteins were detected in the cytoplasm of Sertoli cells in seminiferous tubules of control tissues.
- Intense cytoplasmic and perinuclear staining for mTOR pathway proteins was observed in seminoma cells.
- This study provides the first human evidence of mTOR signaling pathway protein immunoreactivity in testicular seminoma.
Conclusions:
- The mTOR signaling pathway is significantly associated with testicular seminoma.
- Aberrant expression of mTOR pathway proteins in seminoma suggests their potential role in tumorigenesis.
- mTOR signaling components represent potential novel therapeutic targets for testicular seminoma and future male infertility treatments.
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