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The host cell DNA and transcription machinery is a complex system of enzymes and proteins responsible for replicating the genome and transcribing genetic information into RNA [1]. This machinery includes key components such as DNA polymerases, RNA polymerases (particularly RNA polymerase II), and various transcription factors that regulate gene expression [1, 3]. Many pathogens, especially viruses, hijack these host processes to replicate their own genetic material and produce viral proteins [3]. In oncology and virology, this system is targeted by drugs like intercalating agents (e.g., Actinomycin D) and polymerase inhibitors to halt the proliferation of malignant cells or viral replication [2, 4]. However, because these processes are essential for the survival of all healthy cells, drugs targeting the host machinery often face significant challenges regarding systemic toxicity and a narrow therapeutic window [4]. Consequently, while historically significant in chemotherapy and antiviral research, modern drug discovery tends to focus on more specific components within this machinery to improve therapeutic indices.
Inhibition of RNA polymerase, DNA intercalation, inhibition of transcription factors, and disruption of DNA template function.
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