Literature DB >> 30421440

Therapeutic strategies involving survivin inhibition in cancer.

David Martínez-García1,2, Noemí Manero-Rupérez1,3, Roberto Quesada4, Luís Korrodi-Gregório1, Vanessa Soto-Cerrato1,2.   

Abstract

Survivin is a small protein that belongs to the inhibitor of apoptosis protein family. It is abundantly expressed in tumors compared with adult differentiated tissues, being associated with poor prognosis in many human neoplasms. This apoptotic inhibitor has a relevant role in both the promotion of cancer cell survival and in the inhibition of cell death. Consequently, aberrant survivin expression stimulates tumor progression and confers resistance to several therapeutic strategies in a variety of tumors. In fact, efficient survivin downregulation or inhibition results in spontaneous apoptosis or sensitization to chemotherapy and radiotherapy. Therefore, all these features make survivin an attractive therapeutic target to treat cancer. Currently, there are several survivin inhibitors under clinical evaluation, although more specific and efficient survivin inhibitors are being developed. Moreover, novel combination regimens targeting survivin together with other therapeutic approaches are currently being designed and assessed. In this review, recent progress in the therapeutic options targeting survivin for cancer treatment is analyzed. Direct survivin inhibitors and their current development status are explored. Besides, the major signaling pathways implicated in survivin regulation are described and different therapeutic approaches involving survivin indirect inhibition are evaluated. Finally, promising novel inhibitors under preclinical or clinical evaluation as well as challenges of developing survivin inhibitors as a new therapy for cancer treatment are discussed.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  SMAC mimetics; anticancer therapy; apoptosis; chemoresistance; inhibitor of apoptosis proteins; survivin inhibitors

Mesh:

Substances:

Year:  2018        PMID: 30421440     DOI: 10.1002/med.21547

Source DB:  PubMed          Journal:  Med Res Rev        ISSN: 0198-6325            Impact factor:   12.944


  35 in total

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