硫化氢是一种胶质母细胞瘤抑制剂,在高脂肪饮食中会减少。

IF 2.6 Q3 ONCOLOGY Molecular and Cellular Oncology Pub Date : 2021-09-16 eCollection Date: 2021-01-01 DOI:10.1080/23723556.2021.1973312
Daniel J Silver, Justin D Lathia, Christopher Hine
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引用次数: 0

摘要

胶质母细胞瘤(GBM)是最致命和侵袭性的脑癌之一。环境和内在因素,如西方饮食和高龄,对GBM的发展起着强大的促进作用。最近,我们发现临床前GBM模型受致肥性和加速衰老的高脂肪饮食(HFD)影响,呈现出高侵袭性GBM表型,包括治疗难治性癌症干细胞(CSC)富集。从机制上讲,HFD抑制了脑内气体递质硫化氢(H2S)及其下游硫化氢信号的产生。同样地,我们观察到GBM患者大脑中巯基化的显著丧失。重要的是,我们在细胞培养和体内实验中发现了H2S对GBM的肿瘤抑制作用。在这里,我们讨论了这些最新发现,并提供了如何利用它们来改善GBM患者的治疗方式、预后和生活质量的见解。
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Hydrogen sulfide operates as a glioblastoma suppressor and is lost under high fat diet.

Glioblastoma (GBM) is one of the deadliest and aggressive forms of brain cancer. Environmental and intrinsic factors such as Western Diet and advanced age can function as powerful accelerants to the progression of GBM. Recently, we discovered that pre-clinical GBM models subject to an obesogenic and age-accelerating high fat diet (HFD) presented with hyperaggressive GBM phenotypes, including treatment-refractory cancer stem cell (CSC) enrichment. Mechanistically, HFD suppressed production of the gasotransmitter hydrogen sulfide (H2S) and its downstream sulfhydration signaling in the brain. Likewise, we observed dramatic loss of sulfhydration in brains of GBM patients. Importantly, we showed the tumor suppressive effects of H2S against GBM in cell culture and in vivo. Here, we discuss these recent findings and provide insight into how they can be leveraged to improve treatment modalities, prognosis, and quality of life for GBM patients.

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来源期刊
Molecular and Cellular Oncology
Molecular and Cellular Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
3.20
自引率
0.00%
发文量
18
期刊介绍: For a long time, solid neoplasms have been viewed as relatively homogeneous entities composed for the most part of malignant cells. It is now clear that tumors are highly heterogeneous structures that evolve in the context of intimate interactions between cancer cells and endothelial, stromal as well as immune cells. During the past few years, experimental and clinical oncologists have witnessed several conceptual transitions of this type. Molecular and Cellular Oncology (MCO) emerges within this conceptual framework as a high-profile forum for the publication of fundamental, translational and clinical research on cancer. The scope of MCO is broad. Submissions dealing with all aspects of oncogenesis, tumor progression and response to therapy will be welcome, irrespective of whether they focus on solid or hematological neoplasms. MCO has gathered leading scientists with expertise in multiple areas of cancer research and other fields of investigation to constitute a large, interdisciplinary, Editorial Board that will ensure the quality of articles accepted for publication. MCO will publish Original Research Articles, Brief Reports, Reviews, Short Reviews, Commentaries, Author Views (auto-commentaries) and Meeting Reports dealing with all aspects of cancer research.
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