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Updated: Jun 12, 2026

Techniques to Induce and Quantify Cellular Senescence
Published on: May 1, 2017
Therapy-Induced Senescence: Novel Approaches for Markers Identification.
Francesco Pacifico1, Fulvio Magni2, Antonio Leonardi3
1Istituto per l'Endocrinologia e l'Oncologia Sperimentale, CNR, Via S. Pansini 5, 80131 Naples, Italy.
Therapy-induced senescence (TIS) harms cancer patients by promoting tumor growth and relapse. Identifying biomarkers for TIS cells is crucial for developing effective senotherapy to improve patient outcomes.
Area of Science:
- Oncology
- Cellular Biology
- Immunology
Background:
- Therapy-induced senescence (TIS) is a cellular response to cancer treatments.
- Senescent cells, via their senescence-associated secretory phenotype (SASP), can promote tumor growth and hinder anti-tumor immunity.
- Senescent cancer cells may evade growth arrest, potentially leading to relapse.
Purpose of the Study:
- To review current knowledge on TIS in cancer.
- To identify critical knowledge gaps regarding TIS.
- To discuss advances in discovering TIS biomarkers.
Main Methods:
- Literature review of TIS and senotherapy.
- Analysis of the role of SASP in the tumor microenvironment.
- Exploration of current and novel TIS biomarker discovery approaches.
Main Results:
- TIS can negatively impact cancer therapy outcomes.
- Senotherapy, targeting senescent cells or their SASP, is a promising therapeutic strategy.
- A lack of reliable TIS biomarkers impedes clinical translation of senotherapy.
Conclusions:
- TIS presents a significant challenge in cancer therapy.
- Development of TIS biomarkers is a high priority for clinical senotherapy.
- Further research into TIS biomarkers is essential for improving cancer treatment efficacy.
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