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髓系恶性肿瘤中的刺猬信号通路

Hedgehog Signaling in Myeloid Malignancies.

作者信息

Abraham Ajay, Matsui William

机构信息

Department of Oncology, Dell Medical School, University of Texas at Austin, Austin, TX 78712, USA.

出版信息

Cancers (Basel). 2021 Sep 29;13(19):4888. doi: 10.3390/cancers13194888.

Abstract

Myeloid malignancies arise from normal hematopoiesis and include several individual disorders with a wide range of clinical manifestations, treatment options, and clinical outcomes. The Hedgehog (HH) signaling pathway is aberrantly activated in many of these diseases, and glasdegib, a Smoothened (SMO) antagonist and HH pathway inhibitor, has recently been approved for the treatment of acute myeloid leukemia (AML). The efficacy of SMO inhibitors in AML suggests that they may be broadly active, but clinical studies in other myeloid malignancies have been largely inconclusive. We will discuss the biological role of the HH pathway in normal hematopoiesis and myeloid malignancies and review clinical studies targeting HH signaling in these diseases. In addition, we will examine SMO-independent pathway activation and highlight potential strategies that may expand the clinical utility of HH pathway antagonists.

摘要

髓系恶性肿瘤起源于正常造血过程,包括多种具有广泛临床表现、治疗选择和临床结局的个体疾病。刺猬信号通路(HH信号通路)在许多此类疾病中被异常激活,而格拉斯吉布(一种 smoothened(SMO)拮抗剂和HH信号通路抑制剂)最近已被批准用于治疗急性髓系白血病(AML)。SMO抑制剂在AML中的疗效表明它们可能具有广泛的活性,但在其他髓系恶性肿瘤中的临床研究大多尚无定论。我们将讨论HH信号通路在正常造血和髓系恶性肿瘤中的生物学作用,并回顾针对这些疾病中HH信号的临床研究。此外,我们将研究不依赖SMO的信号通路激活,并强调可能扩大HH信号通路拮抗剂临床应用的潜在策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ec8/8507617/d666058928f3/cancers-13-04888-g001.jpg

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