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Updated: May 9, 2026

Laser-capture Microdissection of Human Prostatic Epithelium for RNA Analysis
Published on: November 26, 2015
Down-regulation and aberrant cytoplasmic expression of GLTSCR2 in prostatic adenocarcinomas
Jee-Youn Kim1, Young-Eun Cho, Gou Young Kim
1Department of Pathology, School of Medicine, Kyung Hee University, Seoul 130-701, Republic of Korea.
Abstract:
GLTSCR2 is a nuclear/nucleolar protein that translocates to the nucleoplasm, suppressed and mutated in human cancers. Our aim in this study was to investigate whether downregulation or cytoplasmic expression of GLTSCR2 has any pathological significance in prostatic cancer development or progression. In this study we show that GLTSCR2 is suppressed in prostatic cancers and its expression is significantly associated with Gleason's scores. Furthermore, we investigated the pathogenetic mechanism of downregulation and cytoplasmic expression of GLTSCR2 in development or progression of prostatic cancers. Taken together, our results indicate that GLTSCR2 functions as a tumor suppressor in prostatic adenocarcinomas.
Insights
Glial tumor suppressor candidate 2 (GLTSCR2) is suppressed in prostate cancer, with its reduced expression linked to higher Gleason scores. This suggests GLTSCR2 acts as a tumor suppressor in prostate adenocarcinoma development.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Glial tumor suppressor candidate 2 (GLTSCR2) is a nuclear/nucleolar protein implicated in human cancers.
- Previous studies indicate GLTSCR2 is suppressed and mutated in various human cancers.
- The role of GLTSCR2 in prostate cancer development and progression remains largely unexplored.
Purpose of the Study:
- To investigate the pathological significance of GLTSCR2 downregulation and cytoplasmic expression in prostate cancer.
- To determine the association between GLTSCR2 expression levels and clinicopathological features, such as Gleason's score.
- To elucidate the pathogenetic mechanisms underlying GLTSCR2 alterations in prostate cancer.
Main Methods:
- Analysis of GLTSCR2 expression in prostate cancer tissues and adjacent normal tissues.
- Correlation of GLTSCR2 expression with Gleason's scores and other clinicopathological parameters.
- Investigation of molecular mechanisms driving GLTSCR2 downregulation and cytoplasmic translocation.
Main Results:
- GLTSCR2 expression is significantly suppressed in prostate cancers compared to normal tissues.
- Reduced GLTSCR2 expression and cytoplasmic localization are associated with higher Gleason's scores.
- The study identified pathogenetic mechanisms contributing to GLTSCR2 suppression and altered localization.
Conclusions:
- GLTSCR2 functions as a tumor suppressor in prostatic adenocarcinomas.
- Downregulation and cytoplasmic expression of GLTSCR2 are significant indicators of prostate cancer progression.
- Targeting GLTSCR2 may offer a potential therapeutic strategy for prostate cancer.
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