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茚地那韦对人乳头瘤病毒阳性和阴性头颈癌均显示出抗癌作用。

Indisulam Shows an Anti-Cancer Effect on HPV+ and HPV- Head and Neck Cancer.

作者信息

Hosseini Tara M, Jang Sophie S, Bendik Joseph, Guo Theresa

机构信息

Moores Cancer Center, University of California San Diego, La Jolla, CA 92093, USA.

Department of Otolaryngology-Head & Neck Surgery, University of California San Diego, La Jolla, CA 92093, USA.

出版信息

Cancers (Basel). 2025 Mar 22;17(7):1072. doi: 10.3390/cancers17071072.

DOI:10.3390/cancers17071072
PMID:40227602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11987906/
Abstract

: HPV+ head and neck squamous cell carcinoma has been shown to have a unique genomic background, requiring researchers to study it as its own distinct type of cancer. HPV+ tumors have been shown to exhibit fewer genetic mutations in cancer drivers as opposed to their HPV- counterparts. In this paper, we explored how targeting post-transcriptional changes, specifically alternative splicing events, could serve as a potential mechanism to treat HPV+ cancer. : Using indisulam, a drug that targets alternative splicing through the degradation of RBM39, we treated various HPV+ and HPV- cell lines and assessed tumor cell viability. We also tested indisulam in vivo to evaluate its effect on tumor volume. Additionally, we analyzed gene expression differences between indisulam-treated subjects and their non-treated counterparts. : Indisulam treatment led to a reduction in tumor cell viability in both HPV+ and HPV- cell lines. In vivo experiments showed a reduction in tumor volume following indisulam treatment. Gene expression analysis revealed that indisulam induces consistent differential gene expression changes and highly enriches interferon pathways in treated HPV+ cell lines. : These findings suggest that targeting alternative splicing via indisulam may be a promising therapeutic approach for HPV+ cancers. Further research is required to establish indisulam as a viable anti-cancer treatment in clinical settings.

摘要

人乳头瘤病毒(HPV)阳性的头颈部鳞状细胞癌已被证明具有独特的基因组背景,这就要求研究人员将其作为一种独特的癌症类型来进行研究。与HPV阴性的肿瘤相比,HPV阳性肿瘤在癌症驱动基因中表现出较少的基因突变。在本文中,我们探讨了靶向转录后变化,特别是可变剪接事件,如何能够作为一种治疗HPV阳性癌症的潜在机制。

我们使用因地司他(indisulam),一种通过降解RBM39来靶向可变剪接的药物,对各种HPV阳性和HPV阴性细胞系进行处理,并评估肿瘤细胞的活力。我们还在体内测试了因地司他,以评估其对肿瘤体积的影响。此外,我们分析了因地司他处理组和未处理组之间的基因表达差异。

因地司他处理导致HPV阳性和HPV阴性细胞系中的肿瘤细胞活力均降低。体内实验表明,因地司他处理后肿瘤体积减小。基因表达分析显示,因地司他在处理后的HPV阳性细胞系中诱导一致的差异基因表达变化,并高度富集干扰素通路。

这些发现表明,通过因地司他靶向可变剪接可能是一种治疗HPV阳性癌症的有前景的治疗方法。需要进一步的研究来将因地司他确立为临床环境中可行的抗癌治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74c/11987906/97782cc17618/cancers-17-01072-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74c/11987906/8d45fc630aff/cancers-17-01072-g0A1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74c/11987906/4abc4816aace/cancers-17-01072-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74c/11987906/45f41b003b56/cancers-17-01072-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74c/11987906/edfa841661a4/cancers-17-01072-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74c/11987906/97782cc17618/cancers-17-01072-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74c/11987906/8d45fc630aff/cancers-17-01072-g0A1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74c/11987906/4abc4816aace/cancers-17-01072-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74c/11987906/45f41b003b56/cancers-17-01072-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74c/11987906/edfa841661a4/cancers-17-01072-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74c/11987906/97782cc17618/cancers-17-01072-g004.jpg

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本文引用的文献

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Pharmacological depletion of RNA splicing factor RBM39 by indisulam synergizes with PARP inhibitors in high-grade serous ovarian carcinoma.依地司他联合 PARP 抑制剂抑制 RNA 剪接因子 RBM39 可增强高级别浆液性卵巢癌疗效。
Cell Rep. 2023 Oct 31;42(10):113307. doi: 10.1016/j.celrep.2023.113307. Epub 2023 Oct 19.
2
Indisulam exerts anticancer effects via modulation of transcription, translation and alternative splicing on human cervical cancer cells.茚地那韦通过对人宫颈癌细胞的转录、翻译和可变剪接的调节发挥抗癌作用。
Am J Cancer Res. 2023 Jul 15;13(7):2922-2937. eCollection 2023.
3
The aryl sulfonamide indisulam inhibits gastric cancer cell migration by promoting the ubiquitination and degradation of the transcription factor ZEB1.
芳基磺酰胺类药物 indisulam 通过促进转录因子 ZEB1 的泛素化和降解来抑制胃癌细胞迁移。
J Biol Chem. 2023 Apr;299(4):103025. doi: 10.1016/j.jbc.2023.103025. Epub 2023 Feb 15.
4
Alteration of the IFN-Pathway by Human Papillomavirus Proteins: Antiviral Immune Response Evasion Mechanism.人乳头瘤病毒蛋白对干扰素通路的改变:抗病毒免疫反应逃避机制
Biomedicines. 2022 Nov 17;10(11):2965. doi: 10.3390/biomedicines10112965.
5
Systematic pan-cancer analysis identifies RBM39 as an immunological and prognostic biomarker.系统泛癌症分析确定 RBM39 为免疫和预后生物标志物。
J Cell Mol Med. 2022 Sep;26(18):4859-4871. doi: 10.1111/jcmm.17517. Epub 2022 Aug 21.
6
Indisulam targets RNA splicing and metabolism to serve as a therapeutic strategy for high-risk neuroblastoma.英地舒单抗针对 RNA 剪接和代谢,作为高危神经母细胞瘤的治疗策略。
Nat Commun. 2022 Mar 16;13(1):1380. doi: 10.1038/s41467-022-28907-3.
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Targeting the spliceosome through RBM39 degradation results in exceptional responses in high-risk neuroblastoma models.通过RBM39降解靶向剪接体在高危神经母细胞瘤模型中产生了显著的反应。
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