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针对卡波西肉瘤相关疱疹病毒引起的恶性肿瘤中的缺氧诱导因子

Targeting hypoxia-inducible factors in malignancies caused by Kaposis sarcoma associated herpesvirus.

作者信息

Davis David A, Shrestha Prabha, Yarchoan Robert

机构信息

HIV and AIDS Malignancy Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, USA.

出版信息

Glob Health Med. 2024 Oct 31;6(5):282-284. doi: 10.35772/ghm.2024.01069.

DOI:10.35772/ghm.2024.01069
PMID:39483452
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11514629/
Abstract

In this editorial, we highlight the potential use of inhibitors of hypoxia-inducible factors (HIFs) for the use in Kaposi's sarcoma associated herpesvirus (KSHV) (also known as human herpesvirus-8) related malignancies. The past 20 years has accumulated detailed knowledge of the role of these factors in ensuring the maintenance of the KSHV in infected cells, in aiding the growth of the virus infected cells and aiding in the spread of virus from infected cells by inducing lytic reactivation. Today, a wide range of inhibitors for HIFs are currently being clinically evaluated for use in treating a variety of cancers. We discuss the current state of this research area as it relates to KSHV malignancies and describe pre-clinical and clinical evidence of drugs that target HIF to back up the idea that these inhibitors could be a novel way to treat KSHV related diseases.

摘要

在这篇社论中,我们强调了缺氧诱导因子(HIFs)抑制剂在卡波西肉瘤相关疱疹病毒(KSHV,也称为人类疱疹病毒8型)相关恶性肿瘤中的潜在应用。在过去20年里,我们已经积累了关于这些因子在确保KSHV在受感染细胞中维持、帮助病毒感染细胞生长以及通过诱导裂解再激活帮助病毒从受感染细胞中传播方面所起作用的详细知识。如今,多种HIFs抑制剂正在进行临床评估,用于治疗各种癌症。我们讨论了该研究领域与KSHV恶性肿瘤相关的当前状况,并描述了靶向HIF的药物的临床前和临床证据,以支持这些抑制剂可能是治疗KSHV相关疾病的新方法这一观点。

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Glob Health Med. 2024 Oct 31;6(5):282-284. doi: 10.35772/ghm.2024.01069.
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本文引用的文献

1
Hypoxia and hypoxia-inducible factors in Kaposi sarcoma-associated herpesvirus infection and disease pathogenesis.卡波西肉瘤相关疱疹病毒感染和疾病发病机制中的缺氧和缺氧诱导因子。
J Med Virol. 2023 Sep;95(9):e29071. doi: 10.1002/jmv.29071.
2
Clinical management of Kaposi sarcoma herpesvirus-associated diseases: an update on disease manifestations and treatment strategies.卡波西肉瘤疱疹病毒相关疾病的临床管理:疾病表现和治疗策略的更新。
Expert Rev Anti Infect Ther. 2023 Jul-Dec;21(9):929-941. doi: 10.1080/14787210.2023.2247161. Epub 2023 Aug 15.
3
Echinomycin as a promising therapeutic agent against KSHV-related malignancies.表鬼臼毒素作为一种有前途的治疗药物,可对抗与 KSHV 相关的恶性肿瘤。
J Hematol Oncol. 2023 May 4;16(1):48. doi: 10.1186/s13045-023-01441-5.
4
3-[(1,2,3)-2,3-Difluoro-1-hydroxy-7-methylsulfonylindan-4-yl]oxy-5-fluorobenzonitrile (PT2977), a Hypoxia-Inducible Factor 2α (HIF-2α) Inhibitor for the Treatment of Clear Cell Renal Cell Carcinoma.3-[(1,2,3)-2,3-二氟-1-羟基-7-甲磺酰基-1H-吲唑-4-基]氧基-5-氟苯甲腈(PT2977),一种缺氧诱导因子 2α(HIF-2α)抑制剂,用于治疗肾透明细胞癌。
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The transcriptional factors HIF-1 and HIF-2 and their novel inhibitors in cancer therapy.在癌症治疗中,转录因子 HIF-1 和 HIF-2 及其新型抑制剂。
Expert Opin Drug Discov. 2019 Jul;14(7):667-682. doi: 10.1080/17460441.2019.1613370. Epub 2019 May 9.
6
Hypoxia-inducible factor-1 alpha as a therapeutic target for primary effusion lymphoma.缺氧诱导因子-1α作为原发性渗出性淋巴瘤的治疗靶点。
PLoS Pathog. 2017 Sep 18;13(9):e1006628. doi: 10.1371/journal.ppat.1006628. eCollection 2017 Sep.
7
Multi-targeted therapy of everolimus in Kaposi's sarcoma associated herpes virus infected primary effusion lymphoma.依维莫司治疗人疱疹病毒 8 型感染性原发性渗出性淋巴瘤的多靶点疗法。
Apoptosis. 2017 Sep;22(9):1098-1115. doi: 10.1007/s10495-017-1391-1.
8
Glycolysis, Glutaminolysis, and Fatty Acid Synthesis Are Required for Distinct Stages of Kaposi's Sarcoma-Associated Herpesvirus Lytic Replication.卡波西肉瘤相关疱疹病毒裂解复制的不同阶段需要糖酵解、谷氨酰胺分解和脂肪酸合成。
J Virol. 2017 Apr 28;91(10). doi: 10.1128/JVI.02237-16. Print 2017 May 15.
9
Pomalidomide for Symptomatic Kaposi's Sarcoma in People With and Without HIV Infection: A Phase I/II Study.泊马度胺用于有或无HIV感染的有症状卡波西肉瘤患者:一项I/II期研究。
J Clin Oncol. 2016 Dec;34(34):4125-4131. doi: 10.1200/JCO.2016.69.3812. Epub 2016 Oct 31.
10
Immunomodulatory drugs target IKZF1-IRF4-MYC axis in primary effusion lymphoma in a cereblon-dependent manner and display synergistic cytotoxicity with BRD4 inhibitors.免疫调节药物以一种依赖于cereblon的方式靶向原发性渗出性淋巴瘤中的IKZF1-IRF4-MYC轴,并与BRD4抑制剂显示出协同细胞毒性。
Oncogene. 2016 Apr 7;35(14):1797-810. doi: 10.1038/onc.2015.245. Epub 2015 Jun 29.