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Apoptosis in schistosomes: toward novel targets for the treatment of schistosomiasis

Journal

TRENDS IN PARASITOLOGY
Volume 30, Issue 2, Pages 75-84

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.pt.2013.12.005

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Funding

  1. National Health and Medical Research Council (NHMRC) [1002227]
  2. NHMRC Career Development Fellowship [1024620]
  3. Early Career Development Fellowship [1036194]
  4. Australian Research Council (ARC)
  5. Melbourne Water Corporation
  6. Alexander von Humboldt Foundation
  7. NI-EMRC Independent Research Institute Infrastructure Support Scheme (IRIISS) [361646]
  8. Victorian State Government Operational Infrastructure Support (OIS)

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Schistosomiasis is one of the world's major neglected tropical diseases. Recent advances in schistosome genomics and transcriptomics have identified components of an intrinsic, B cell lymphoma-2 (BcI-2)-regulated apoptotic cell death pathway. Molecular characterization of this pathway demonstrates its similarity to that in mammals. Gene expression and functional data indicate that apoptosis is active throughout the lifecycle. Moreover, drugs that activate apoptosis in human cells kill schistosome cells, raising the prospect of developing new treatments against schistosomiasis of humans. The development of new drugs is increasingly important in the face of the potential for resistance to currently available treatments, and the lack of an effective vaccine.

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