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Review article

Survivin, a molecular target for therapeutic interventions in squamous cell carcinoma

Zakir KhanDepartment of Biomedical Sciences, Department of Pathology, Cedars-Sinai Medical Center, Los Angeles, CA 90048 USAAbdul Arif KhanDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi ArabiaHariom YadavNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892 USAGodavarthi B.K.S. PrasadSchool of Studies in Biotechnology, Jiwaji University, Gwalior, 474001 MP IndiaPrakash S. BisenSchool of Studies in Biotechnology, Jiwaji University, Gwalior, 474001 MP India
2017en
ABI

Abstract

Squamous cell carcinoma (SCC) is the most common cancer worldwide. The treatment of locally advanced disease generally requires various combinations of radiotherapy, surgery, and systemic therapy. Despite aggressive multimodal treatment, most of the patients relapse. Identification of molecules that sustain cancer cell growth and survival has made molecular targeting a feasible therapeutic strategy. Survivin is a member of the Inhibitor of Apoptosis Protein (IAP) family, which is overexpressed in most of the malignancies including SCC and totally absent in most of the normal tissues. This feature makes survivin an ideal target for cancer therapy. It orchestrates several important mechanisms to support cancer cell survival including inhibition of apoptosis and regulation of cell division. Overexpression of survivin in tumors is also associated with poor prognosis, aggressive tumor behavior, resistance to therapy, and high tumor recurrence. Various strategies have been developed to target survivin expression in cancer cells, and their effects on apoptosis induction and tumor growth attenuation have been demonstrated. In this review, we discuss recent advances in therapeutic potential of survivin in cancer treatment.

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Cited by 20 references