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Updated: May 21, 2026

Evaluating the Effectiveness of Cancer Drug Sensitization In Vitro and In Vivo
Published on: February 6, 2015
Survivin signaling in clinical oncology: a multifaceted dragon
Jagat R Kanwar1, Sishir K Kamalapuram, Rupinder K Kanwar
1Nanomedicine-Laboratory of Immunology and Molecular Biomedical Research, Centre for Biotechnology and Interdisciplinary Biosciences, Institute for Technology & Research Innovation, Deakin University, Geelong, Victoria, Australia. jagat.kanwar@deakin.edu.au
Abstract:
Survivin is an inhibitor of apoptosis protein (IAP) family member preferentially expressed in a myriad of clinical cancers. The complex functional mechanism and regulatory roles of survivin in cell division and cell death has hindered current therapeutic regimes from decoding its diagnostic, prognostic, and therapeutic significance in the area of translational oncology. Pharmacological modulation of survivin was tagged with its evolving functional complexity associated with various cell-signaling cascades including PI3K/AKT, mammalian target of rapamycin (mTOR), extracellular signal-regulated kinases (ERK), mitogen-activated protein kinases (MAPK), signal transducer and activator of transcription (STAT), hypoxia-inducible factor-1α (HIF-1α), heat-shock protein 90 (HSP90), p53, B-cell lymphoma 2 (Bcl2), epidermal growth factor receptor (EGFR), vascular endothelial growth factor (VEGF) etc. The present review provides a multifaceted role of survivin and its mechanistic action in an array of clinical cancers. Furthermore, the utilization of novel nanotechnology-based drug delivery systems for target-specific hurling of tumors enabling contemporaneous detection, treatment, and therapeutic imaging in cancer therapy are discussed.
Insights
Survivin, a key protein in cancer, regulates cell division and death. Understanding its complex roles and targeting it with nanotechnology offers new cancer treatment strategies.
Area of Science:
- Oncology
- Molecular Biology
- Nanotechnology
Background:
- Survivin is an inhibitor of apoptosis protein (IAP) family member highly expressed in various clinical cancers.
- Its complex functional mechanisms in cell division and death present challenges for current therapeutic strategies in translational oncology.
- Survivin's significance in cancer diagnosis, prognosis, and therapy is not fully decoded due to its intricate roles.
Purpose of the Study:
- To review the multifaceted roles and mechanistic actions of survivin in diverse clinical cancers.
- To discuss the involvement of survivin in various cell-signaling cascades.
- To explore the application of nanotechnology-based drug delivery systems for targeted cancer therapy.
Main Methods:
- Literature review of survivin's function and regulation in cancer.
- Analysis of survivin's involvement in key signaling pathways (e.g., PI3K/AKT, MAPK, STAT, HIF-1α, EGFR, VEGF).
- Discussion of nanotechnology-based approaches for survivin-targeted drug delivery.
Main Results:
- Survivin plays a complex role in cell division and apoptosis, impacting cancer progression.
- Pharmacological modulation of survivin is linked to numerous cell-signaling cascades.
- Nanotechnology offers potential for targeted tumor delivery, detection, and treatment.
Conclusions:
- Survivin is a critical target in oncology due to its roles in cell division and death.
- Targeting survivin through novel drug delivery systems, particularly nanotechnology, holds promise for improved cancer treatment.
- Further research into survivin's mechanisms and nanodelivery systems is crucial for advancing cancer therapy.
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