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Updated: Jan 9, 2026

Strategies for Tracking Anastasis, A Cell Survival Phenomenon that Reverses Apoptosis
Published on: February 16, 2015
Targeting Survivin: Now I Become Death, the Destroyer of Cells
Mia Fanuzzi1,2, Shuhua Zheng2,3, Craig M Horbinski1,2
1Department of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Abstract:
Survivin (BIRC5) plays a key role in inhibiting apoptosis and is highly expressed in many cancers, including gliomas and breast cancer, where it contributes to tumor progression, therapeutic resistance and poor patient outcomes. With a dual function in promoting cell proliferation and survival, coupled with its potential immunogenicity, survivin is a compelling therapeutic target for cancer; yet, it has no FDA-approved agents to date. Here, we review key findings from preclinical models that emphasize how survivin contributes to chemoresistance and radioresistance; summarize the clinical landscape of survivin-targeted strategies, highlighting both the successes and limitations of these approaches; and outline next steps to optimize survivin-targeted therapies, including the need to integrate biomarker-focused patient selection and the potential for combination therapies. These insights establish survivin as a key driver of cancer progression and a promising target for future therapeutic development.
Insights
Survivin (BIRC5) drives cancer progression and resistance to therapy. Targeting survivin offers a promising strategy for future cancer treatments, though further optimization is needed.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Therapeutics
Background:
- Survivin (BIRC5) is highly expressed in cancers like glioma and breast cancer, promoting tumor progression and therapeutic resistance.
- Its role in inhibiting apoptosis and promoting cell proliferation makes it a significant factor in poor patient outcomes.
Purpose of the Study:
- To review preclinical findings on survivin's role in chemoresistance and radioresistance.
- To summarize the clinical landscape of survivin-targeted therapies, including successes and limitations.
- To outline strategies for optimizing future survivin-targeted treatments.
Main Methods:
- Review of preclinical models demonstrating survivin's contribution to therapeutic resistance.
- Analysis of clinical trial data for survivin-targeted strategies.
- Synthesis of current knowledge to propose future therapeutic directions.
Main Results:
- Preclinical data confirm survivin's role in chemoresistance and radioresistance.
- Clinical strategies targeting survivin have shown both promise and limitations.
- Biomarker-driven patient selection and combination therapies are key for optimization.
Conclusions:
- Survivin is a critical driver of cancer progression and therapeutic resistance.
- Targeting survivin presents a promising avenue for cancer therapy development.
- Future strategies should focus on patient selection and combination approaches for enhanced efficacy.
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