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新兴的抗恶性胶质瘤重组溶瘤脊髓灰质炎病毒疗法综述

Emerging Recombinant Oncolytic Poliovirus Therapies Against Malignant Glioma: A Review.

作者信息

Dighe Onkar R, Korde Paresh, Bisen Yuganshu T, Iratwar Sandeep, Kesharwani Anukriti, Vardhan Sauvik, Singh Abhinesh

机构信息

Department of Neurosurgery, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.

出版信息

Cureus. 2023 Jan 21;15(1):e34028. doi: 10.7759/cureus.34028. eCollection 2023 Jan.

Abstract

Glioblastoma multiforme (GBM) is a fourth-grade malignant glioma that continues to be the main contributor to primary malignant brain tumour-related death in humans. The most prevalent primary brain tumours are gliomas. The most dangerous of these neoplasms, GBM, has been shown to be one of the most lethal and refractory tumours. For those who have been diagnosed with GBM, the median time to progression, as determined by magnetic resonance imaging, is roughly six months, and the median survival is approximately one year. GBM is challenging to manage with old treatments like chemotherapy, tumour debulking, and radiation therapy. Treatment outcomes are poor, and due to this effect, the treatment is not up to the mark. GBM also shows diagnostic complexity due to limitations in the use of specific targeted therapies. The treatment protocol followed currently has an entire focus on safe resection and radiotherapy. Protein synthesis is not tightly regulated physiologically in malignant cells, which promotes unchecked growth and proliferation. An innovative, experimental technique for treating cancer uses polioviruses that have been genetically altered to target a fascinating aberration of translation regulation in cancer. This approach enables precise and effective cancer cell targeting based on the convergence of numerous variables. Oncolytic viruses have revolutionised cancer treatment. However, their effectiveness in glioblastoma remains restricted, necessitating more improvement. Oncolytic poliovirus has shown great potential in the treatment of GBM. Factors like the blood-brain barrier, immunosuppressive tumour microenvironment (TME), and tumour heterogeneity make treatment for malignant gliomas ineffective. In this review, we have focused on oncolytic viruses, specifically oncolytic poliovirus, and we explore malignant glioma treatments. We have also discussed currently available conventional treatment options for malignant glioma and other brain tumours.

摘要

多形性胶质母细胞瘤(GBM)是一种四级恶性胶质瘤,仍然是人类原发性恶性脑肿瘤相关死亡的主要原因。最常见的原发性脑肿瘤是胶质瘤。这些肿瘤中最危险的GBM已被证明是最致命和最难治疗的肿瘤之一。对于那些被诊断为GBM的患者,通过磁共振成像确定的中位进展时间约为六个月,中位生存期约为一年。GBM很难通过化疗、肿瘤减瘤和放射治疗等传统治疗方法进行管理。治疗效果不佳,因此这种治疗方法并不达标。由于特定靶向治疗的使用存在局限性,GBM的诊断也很复杂。目前遵循的治疗方案完全集中在安全切除和放射治疗上。在恶性细胞中,蛋白质合成在生理上没有受到严格调控,这促进了不受控制的生长和增殖。一种创新的癌症治疗实验技术使用经过基因改造的脊髓灰质炎病毒,以针对癌症中一种引人关注的翻译调控异常。这种方法基于众多变量的汇聚,能够精确有效地靶向癌细胞。溶瘤病毒彻底改变了癌症治疗。然而,它们在胶质母细胞瘤中的有效性仍然有限,需要进一步改进。溶瘤脊髓灰质炎病毒在GBM治疗中显示出巨大潜力。血脑屏障、免疫抑制性肿瘤微环境(TME)和肿瘤异质性等因素使得恶性胶质瘤的治疗效果不佳。在这篇综述中,我们重点关注溶瘤病毒,特别是溶瘤脊髓灰质炎病毒,并探讨恶性胶质瘤的治疗方法。我们还讨论了目前可用于恶性胶质瘤和其他脑肿瘤的传统治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1df/9939956/c8d976e139bb/cureus-0015-00000034028-i01.jpg

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