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Role of Oncoviruses in Cancer Progression and Emerging Phytochemical-Based Therapies from Medicinal Plants
Shivani Singh1, Pardeep Yadav2,3
1Department of Biotechnology, School of Applied and Life Sciences, Uttaranchal University, Dehradun, 248007, Uttarakhand, India.
Abstract:
Oncoviruses continues to be an unattended cause of the global cancer load as they cause about 12-15 % of human malignancies in the world. The oncogenic infections that become persistent, such as Human Papillomavirus (HPV), Epstein-Barr Virus (EBV), Hepatitis B and C viruses (HBV, HCV), Human T cell Leukemia Virus-1 (HTLV-1), and Kaposi Sarcoma-associated Herpesvirus (KSHV), are associated with malignant transformation by continuous destabilization of host cell cycle regulation, immune surveillance, and metabolic homeostasis. These viruses abuse critical oncogenic signaling networks like PI3K/AKT/mTOR, NF -KB, JAK/STAT, MAPK, Wnt/β-catenin, and p53-dependent networks, hence, facilitating unchecked proliferation, chronic inflammation, genomic instability, and tumor progression. Although there have been improvements in the traditional forms of treatment, such as chemotherapy, radiotherapy, antiviral agents, immunotherapy, and gene-based treatments, yet clinical outcomes are still hampered by drug resistance, viral latency, systemic toxicity, and inaccessibility, and other severe side effects especially in low- and middle-income nations. Hence, there is a dire need to introduce new medicinal plant-based therapeutic approaches against oncovirus. This review analyses the molecular pathways of viral oncogenesis critically and discusses the clinical translation and a promising future potential of phytochemicals derived from medicinal plants like Phyllanthus emblica, Datura stramonium, Cannabis sativa, Andrographis paniculata, Aegle marmelos, Calotropis procera, and Prosopis cineraria proven to have bioactive compounds functioning as antivirals, immune-modulator, pro-apoptotic, and cell cycle regulatory effects in the preclinical models along with multi-targets.
Insights
Oncoviruses cause 12-15% of global cancers by disrupting cell regulation. This review explores plant-derived phytochemicals as novel treatments targeting viral oncogenesis pathways, offering hope against drug resistance and side effects.
Area of Science:
- Oncology and Virology: Investigating the role of oncoviruses in human malignancies.
Background:
- Oncoviruses are responsible for 12-15% of global cancer burden, causing persistent infections like HPV, EBV, HBV, HCV, HTLV-1, and KSHV.
- These viruses disrupt host cell cycle regulation, immune surveillance, and metabolic homeostasis, promoting cancer development through critical oncogenic signaling networks.
- Current treatments face challenges including drug resistance, latency, toxicity, and accessibility, particularly in low- and middle-income countries.
Purpose of the Study:
- To critically analyze the molecular pathways of viral oncogenesis.
- To discuss the clinical translation and future potential of medicinal plant-derived phytochemicals as novel anti-oncovirus therapeutics.
Main Methods:
- Literature review focusing on molecular mechanisms of viral oncogenesis.
- Analysis of preclinical data on phytochemicals from selected medicinal plants.
- Evaluation of phytochemicals' antiviral, immune-modulatory, pro-apoptotic, and cell cycle regulatory effects.
Main Results:
- Identified key oncogenic signaling networks (PI3K/AKT/mTOR, NF-κB, JAK/STAT, MAPK, Wnt/β-catenin, p53) exploited by oncoviruses.
- Highlighted phytochemicals from plants like Phyllanthus emblica, Cannabis sativa, and Andrographis paniculata exhibit promising preclinical antiviral and anti-cancer activities.
- Demonstrated multi-target potential of these phytochemicals against viral oncogenesis.
Conclusions:
- Medicinal plant-derived phytochemicals represent a promising therapeutic avenue against oncoviruses, potentially overcoming limitations of current treatments.
- Further research and clinical translation are warranted to harness the multi-target capabilities of these natural compounds for cancer therapy.
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