Gene Fusions in Cancer

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Molecular Cancer Biology".

Deadline for manuscript submissions: 31 March 2026 | Viewed by 17

Special Issue Editors


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Guest Editor
Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia
Interests: cancer genomics; sarcoma; targeted therapies; cancer evolution; drug resistance mechanisms

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Guest Editor
Peter MacCallum Cancer Centre, Melbourne, VIC 3052, Australia
Interests: molecular haematology; drug resistance; measurable residual disease; clonal haematopoiesis; myelodysplastic syndrome; acute myeloid leukaemia

Special Issue Information

Dear Colleagues,

The importance of gene fusions in cancer has been recognised since 1984 when the chronic myeloid leukaemia-associated Philadelphia chromosome was found to result in the fusion of the BCR and ABL1 genes. Since then, oncogenic gene fusions have been shown to be widespread in both haematological malignancies and solid tumours. Their clinical importance may be profound with gene fusions, such as those involving ABL1, ALK or NTRK, representing some of the most successful examples of targeted therapy. Furthermore, many cancers, particularly certain sarcomas and leukaemias, are defined by the presence of a specific oncogenic fusion and they are, thus, diagnostically critical. The advent of whole genome and RNA-based next-generation sequencing technologies over the past decade has resulted in the characterisation of a plethora of novel oncogenic fusions, the molecular pathogeneses and clinical impacts of which largely remain obscure.

This Special Issue will explore recent developments in both the mechanistic and clinical aspects of oncogenic gene fusions.

Dr. Christopher R. McEvoy
Dr. Ing Soo Tiong
Guest Editors

Manuscript Submission Information

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Keywords

  • gene fusions
  • targeted therapy
  • cancer diagnostics
  • molecular pathology

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Published Papers

This special issue is now open for submission.
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