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Syahril Abdullah

Publications and source records attributed to Syahril Abdullah.

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Oncolytic mechanisms and immunotherapeutic potential of Newcastle disease virus in cancer therapy

Newcastle Disease Virus (NDV), classified as Avian orthoavulavirus 1 (avian paramyxovirus type 1), is a promising oncolytic agent that selectively targets and destroys cancer cells while sparing normal tissues. Its oncoselectivity exploits cancer-specific defects in antiviral defenses, particularly impaired Type I interferon signaling, and dysregulated apoptotic pathways, enabling robust viral replication and cytotoxicity in malignancies such as breast, colorectal, and melanoma. NDV induces intrinsic and extrinsic apoptosis through caspase activation and triggers immunogenic cell death via damage-associated molecular patterns, stimulating potent antitumours immune responses. Additionally, NDVs potential as a vaccine vector, expressing tumours-associated antigens, offers prospects for prophylactic and therapeutic cancer applications. This review provides a comprehensive analysis of NDVs morphology, classification, and molecular biology, focusing on its viral entry and replication mechanisms in host cells. It explores NDVs interactions with cancer cells, emphasizing its ability to induce cytotoxicity and immune activation. Understanding these mechanisms is critical for optimizing NDVs oncolytic potential and advancing its clinical translation. Future directions include enhancing NDV through genetic engineering, combining it with therapies like immune checkpoint inhibitors, and developing personalized medicine approaches tailored to tumours genomic profiles. These advancements position NDV as a versatile therapeutic agent in oncolytic virotherapy.

q-bio.BM

Transcriptome profiling research in urothelial cell carcinoma

Urothelial cell carcinoma (UCC) is the ninth most common cancer that accounts for 4.7% of all the new cancer cases globally. UCC development and progression are due to complex and stochastic genetic programmes. To study the cascades of molecular events underlying the poor prognosis that may lead to limited treatment options for advanced disease and resistance to conventional therapies in UCC, transcriptomics technology (RNA-Seq), a method of analysing the RNA content of a sample using modern high-throughput sequencing platforms has been employed. Here we review the principles of RNA-Seq technology and summarize recent studies on human bladder cancer that employed this technique to unravel the pathogenesis of the disease, identify biomarkers, discover pathways and classify the disease state. We list the commonly used computational platforms and software that are publicly available for RNA-Seq analysis. Moreover, we discussed the future perspectives for RNA-Seq studies on bladder cancer and recommend the application of new technology called single cell sequencing (scRNA-Seq) to further understand the disease. Keywords: Transcriptome profiling, RNA-sequencing, genomics, bioinformatics, bladder cancer

q-bio.GN