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Updated: Jul 30, 2025

Techniques to Induce and Quantify Cellular Senescence
Published on: May 1, 2017
Androgen Receptor Activation Induces Senescence in Thyroid Cancer Cells
Anvita Gupta1, Michelle Carnazza1, Melanie Jones1
1Department of Pathology, Microbiology, and Immunology, New York Medical College, Valhalla, NY 10595, USA.
Androgen receptor (AR) activation in thyroid cancer cells induces senescence, a key factor potentially explaining the lower incidence of thyroid cancer (TC) in men. This finding offers novel insights into AR
Area of Science:
- Endocrinology
- Oncology
- Cell Biology
Background:
- Thyroid cancer (TC) is the most common endocrine malignancy, disproportionately affecting women.
- Androgen receptor (AR) RNA is notably downregulated in papillary thyroid cancer (PTC).
Purpose of the Study:
- To investigate the functional role of androgen receptor (AR) activation in thyroid cancer (TC) cells.
- To explore the potential mechanisms underlying sex-based differences in TC incidence.
Main Methods:
- Exposure of anaplastic TC (84E7) and PTC (K1) cells to physiological levels of 5α-dihydrotestosterone (DHT).
- Assessment of cell proliferation, morphology, senescence markers (β-galactosidase, p16, p21, p27), reactive oxygen species, cytokine profiles, and cell migration.
- Analysis of tumor suppressor protein expression and proteolytic invasion potential.
Main Results:
- AR activation significantly decreased proliferation by 80% and induced G1 growth arrest and senescence in TC cells.
- Senescence was characterized by morphological changes, increased senescence markers, and a non-inflammatory secretome.
- Cell migration increased six-fold, while proteolytic invasion remained unchanged.
Conclusions:
- Androgen receptor (AR) activation induces a novel senescence program in thyroid cancer cells.
- This AR-mediated senescence may contribute to the reduced incidence of thyroid cancer observed in men.
- AR activation presents a potential therapeutic avenue for thyroid cancer treatment.
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