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Updated: Aug 2, 2026

Evaluating the Effectiveness of Cancer Drug Sensitization In Vitro and In Vivo
Published on: February 6, 2015
Survivin as a target for new anticancer interventions
Nadia Zaffaroni1, Marzia Pennati, Maria Grazia Daidone
1Dipartimento di Oncologia Sperimentale, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy. nadia.zaffaroni@istitutotumori.mi.it
Abstract:
Survivin is a member of the inhibitor of apoptosis protein (IAP) family, that has been implicated in both control of cell division and inhibition of apoptosis. Specifically, its anti-apoptotic function seems to be related to the ability to directly or indirectly inhibit caspases. Survivin is selectively expressed in the most common human neoplasms and appears to be involved in tumor cell resistance to some anticancer agents and ionizing radiation. On the basis of these findings survivin has been proposed as an attractive target for new anticancer interventions. Several preclinical studies have demonstrated that down-regulation of survivin expression/function, accomplished through the use of antisense oligonucleotides, dominant negative mutants, ribozymes, small interfering RNAs and cyclin-dependent kinase inhibitors, increased the apoptotic rate, reduced tumor-growth potential and sensitized tumor cells to chemotherapeutic drugs with different action mechanisms and gamma-irradiation in in vitro and in vivo models of different human tumor types.
Insights
Survivin protein promotes cancer cell survival and resistance to cancer therapies. Inhibiting survivin can increase cancer cell death and sensitivity to treatments, making it a promising anticancer target.
Area of Science:
- Molecular Biology
- Cancer Biology
- Biochemistry
Background:
- Survivin, an inhibitor of apoptosis protein (IAP) family member, regulates cell division and apoptosis.
- Its anti-apoptotic function involves direct or indirect inhibition of caspases.
- Survivin is highly expressed in human neoplasms and contributes to tumor resistance against anticancer agents and radiation.
Purpose of the Study:
- To investigate survivin as a potential target for novel anticancer interventions.
- To evaluate the effects of down-regulating survivin expression or function on tumor cells.
Main Methods:
- Utilizing preclinical models (in vitro and in vivo) of various human tumor types.
- Employing strategies such as antisense oligonucleotides, dominant negative mutants, ribozymes, small interfering RNAs, and cyclin-dependent kinase inhibitors to down-regulate survivin.
Main Results:
- Down-regulation of survivin significantly increased the apoptotic rate in tumor cells.
- Reduced tumor growth potential was observed following survivin inhibition.
- Survivin-targeted strategies sensitized tumor cells to various chemotherapeutic drugs and gamma-irradiation.
Conclusions:
- Survivin is a critical factor in cancer cell survival and therapeutic resistance.
- Targeting survivin effectively enhances apoptosis and tumor cell sensitivity to anticancer treatments.
- Survivin represents a promising therapeutic target for developing new cancer interventions.
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