4.3 Review

Caspase-9: structure, mechanisms and clinical application

Journal

ONCOTARGET
Volume 8, Issue 14, Pages 23996-24008

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.15098

Keywords

caspase-9; apoptosis; phosphorylation; alternative splicing; iCasp9

Funding

  1. Key Project of National Natural Science Foundation of China [U1232207]
  2. National Key Research and Development Program of the Ministry of Science and Technology of China [2016YFC0904700]
  3. National Key Technology Support Program of the Ministry of Science and Technology of China [2015BAI01B11]
  4. National Natural Science Foundation of China [11305223, 11505245]
  5. Western Talents Program of the Chinese Academy of Sciences [Y562020XB0]

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As the most intensively studied initiator caspase, caspase-9 is a key player in the intrinsic or mitochondrial pathway which is involved in various stimuli, including chemotherapies, stress agents and radiation. Caspase-9 is activated on the apoptosome complex to remain catalytic status and is thought of involving homo-dimerization monomeric zymogens. Failing to activate caspase-9 has profound physiological and pathophysiological outcomes, leading to degenerative and developmental disorders even cancer. To govern the apoptotic commitment process appropriately, plenty of proteins and small molecules involved in regulating caspase-9. Therefore, this review is to summarize recent pertinent literature on the comprehensive description of the molecular events implicated in caspase-9 activation and inhibition, as well as the clinical trials in progress to give deep insight into caspase-9 for suppressing cancer. We hope that our concerns will be helpful for further clinical studies addressing the roles of caspase-9 and its regulators demanded to identify more effective solutions to overcome intrinsic apoptosis-related diseases especially cancer.

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