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Hedgehog pathway inhibition as a therapeutic target in acute myeloid leukemia
Authors:Rory M Shallis  Jan Philipp Bewersdorf  Prajwal C Boddu
Affiliation:1. Division of Hematology, Department of Medicine, Yale University School of Medicine, New Haven, CT, USAORCID Iconhttps://orcid.org/0000-0002-8542-2944;2. Division of Hematology, Department of Medicine, Yale University School of Medicine, New Haven, CT, USAORCID Iconhttps://orcid.org/0000-0003-3352-0902;3. Division of Hematology, Department of Medicine, Yale University School of Medicine, New Haven, CT, USAORCID Iconhttps://orcid.org/0000-0001-9408-5882
Abstract:Introduction: The Hedgehog (HH) pathway constitutes a collection of signaling molecules which critically influence embryogenesis. In adults, however, the HH pathway remains integral to the proliferation, maintenance, and apoptosis of adult stem cells including hematopoietic stem cells.

Areas covered: We discuss the current understanding of the HH pathway as it relates to normal hematopoiesis, the pathology of acute myeloid leukemia (AML), the rationale for and data from combination therapies including HH pathway inhibitors, and ultimately the prospects that might offer promise in targeting this pathway in AML.

Expert opinion: Efforts to target the HH pathway have been focused on impeding this disposition and restoring chemosensitivity to conventional myeloid neoplasm therapies. The year 2018 saw the first approval of a HH pathway inhibitor (glasdegib) for AML, though for an older population and in combination with an uncommonly-used therapy. Several other clinical trials with agents targeting modulators of HH signaling in AML and MDS are underway. Further study and understanding of the interplay between the numerous aspects of HH signaling and how it relates to the augmented survival of AML will provide a more reliable substrate for therapeutic strategies in patients with this poor-risk disease.

Keywords:Acute myeloid leukemia  AML  glasdegib  Hedgehog  myeloid
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