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Abstract

Novel Approaches in Cancer Study

The Role of “Hedgehog Signaling” in AML

  • Open or ClosePavan Kumar Dhanyamraju1*, Yevgeniya Bamme1, Dhimant Desai2, and Sinisa Dovat1

    1Department of Pediatrics, Pennsylvania State University College of Medicine, Hershey, PA 17033, USA

    2Department of Pharmacology, Pennsylvania State University College of Medicine, Hershey, PA 17033, USA

    *Corresponding author:Pavan Kumar Dhanyamraju, Department of Pediatrics, Pennsylvania State University College of Medicine,Hershey-17033, PA, USA, Tel: 717-531-1841, Email: pdhanyamraju@pennstatehealth.psu.edu

Submission: March 18, 2020 Published: April 06, 2020

DOI: 10.31031/NACS.2020.04.000588

ISSN:2637-773X
Volume4 Issue3

Abstract

The Hedgehog (Hh) signal transduction pathway is involved in diverse physiological processes such as cell survival, proliferation, differentiation, embryonic development, and fetal determination. Perturbations in this pathway leading to its aberrant activation have been implicated in various cancers including acute myeloid leukemia (AML). AML is a highly complex hematological malignancy resulting due to accumulation of abnormal myeloblasts in the bone marrow leading to bone marrow failure and ultimately death. Recently, the role of hedgehog signaling in AML pathogenesis has been uncovered and thus pharmacological targeting of the hedgehog pathway in AML has become a prime therapeutic option. In this mini-review, we highlight the role of the hedgehog pathway in AML and review the latest drugs as well as possible Hh targets in treating AML.

Keywords: Hedgehog signaling; Smoothened; Patched; Acute myeloid leukemia; Targets; Drugs; Treatments; Canonical pathway; Noncanonical pathway

Abbreviations: Hedgehog (Hh), Acute Myeloid Leukemia (AML), Desert Hedgehog (DHH), Indian Hedgehog (IHH), GLI1(Glioma-Associated Oncogene Homolog 1), Sonic Hedgehog (SHH), Primary Cilium (PC), Patched (PTCH), Smoothened (SMO), Rhabdomyosarcoma (RMS), Basal Cell Carcinoma (BCC), Adverse Events (AEs), Receptor Tyrosine Kinases (RTKs), Cancer Stem Cells (CSC), Leukemic Stem Cells (LSC), Food and Drug Administration (FDA), Hematopoietic Stem Cell Transplantation (HSCT), Minimal Residual Disease (MRD), UDP-Glucuronosyl Transferase (UGT1A), Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR), GLI Antagonist (GANT61), Bone Marrow (BM)

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