Survivin, an anti-apoptotic molecule abundantly expressed in most human
neoplasms, has been reported to contribute to
cancer initiation and drug resistance in a wide variety of human
tumors. Efficient downregulation of
survivin can sensitize
tumor cells to various therapeutic interventions, generating considerable efforts in its validation as a new target in
cancer therapy. This review thoroughly analyzes up-to-date information on the potential of
survivin as a therapeutic target for new anticancer treatments. The literature dealing with the therapeutic targeting of
survivin will be reviewed, discussing specifically
squamous cell carcinomas (SCCs), and with emphasis on the last clinical trials. This review gives insight into the recent developments undertaken in validating various treatment strategies that target
survivin in SCCs and analyze the translational possibility, identifying those strategies that seem to be the closest to being incorporated into clinical practice. The most recent developments, such as dominant-negative
survivin mutants, RNA interference,
anti-sense oligonucleotides, small-molecule inhibitors, and
peptide-based
immunotherapy, seem to be helpful for effectively downregulating
survivin expression and reducing
tumor growth potential, increasing the apoptotic rate, and sensitizing
tumor cells to chemo- and
radiotherapy. However, selective and efficient targeting of
survivin in clinical trials still poses a major challenge.