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Updated: Jan 18, 2026

Simultaneous Imaging and Flow-Cytometry-based Detection of Multiple Fluorescent Senescence Markers in Therapy-Induced Senescent Cancer Cells
Published on: July 12, 2022
Unraveling senescence in cancer: mechanistic complexities and therapeutic opportunities
Prajakta Tiwari1, Shreesh Kumar Shukla1, Smita Rastogi Verma2
1Department of Biotechnology, Delhi Technological University, Delhi, 110042, India.
Abstract:
Senescence is a pivotal cellular process, which also plays a major role in development, immune regulation, tissue repair, and aging, triggered by stressors such as telomere shortening, oncogene activation, and DNA damage. Characterized by distinct morphological and molecular features, senescence is known to act as a tumor suppressive mechanism through irreversible cell cycle arrest. However, emerging studies reveal a paradox: prolonged senescence in cancer cells can drive tumorigenesis via the senescence-associated secretory phenotype, promoting proliferation, invasion, and metastasis. This comprehensive review elucidates the molecular intricacies of senescence to induce growth arrest, enhance immune surveillance, and favorably modulate the tumor microenvironment to inhibit cancer progression. Additionally, it examines the senescence-inducing effects of conventional therapies and explores the potential of emerging therapies, including targeted therapies and chimeric antigen receptor T cell therapy. The present review also highlights the promise of senotherapeutic strategies in selectively targeting senescent cells to improve therapeutic outcomes. It discusses the innovative integration of machine learning tools for biomarker discovery and patient stratification offering a transformative approach to improve cancer treatment efficacy.
Insights
Cellular senescence, a process involved in aging and tumor suppression, paradoxically promotes cancer via its secretory phenotype. This review explores senescence
Area of Science:
- Cellular Biology
- Oncology
- Immunology
- Aging Research
Background:
- Senescence is a cellular state triggered by stressors, crucial for development, immunity, tissue repair, and aging.
- It acts as a tumor suppressor by arresting cell cycles, but prolonged senescence can paradoxically drive cancer progression.
- The senescence-associated secretory phenotype (SASP) in cancer cells promotes proliferation, invasion, and metastasis.
Purpose of the Study:
- To elucidate the molecular mechanisms of senescence in cancer suppression and progression.
- To review senescence-inducing conventional and emerging cancer therapies.
- To highlight senotherapeutic strategies and machine learning applications in oncology.
Main Methods:
- Comprehensive literature review of senescence in cancer.
- Analysis of molecular pathways regulating senescence.
- Examination of therapeutic strategies targeting senescence.
- Discussion of machine learning for biomarker discovery and patient stratification.
Main Results:
- Senescence can inhibit cancer by inducing growth arrest and enhancing immune surveillance.
- Prolonged senescence and SASP can promote tumorigenesis and metastasis.
- Conventional and novel therapies can induce senescence; senotherapeutics offer targeted approaches.
- Machine learning aids in identifying senescence biomarkers and stratifying cancer patients.
Conclusions:
- Senescence presents a dual role in cancer, acting as both a suppressor and promoter.
- Targeting senescence, particularly senescent cells, holds significant therapeutic promise.
- Integrating machine learning with senescence research can revolutionize cancer treatment efficacy.
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