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Phytochemicals From Mangroves and Their Anti-Viral Applications
have an effective anti-viral nature. Hence, these identified compounds can be used for the repurpos­ing of the drug against other related pathogenic viruses (Murugan et al., 2021; Mahmud et al., 2021; Kharisma et al., 2021).
Figure 4. Year-wise publication of research article when searched in Google scholar (https://scholar. google.com/) with the keyword antiviral compounds and Mangrove plant.
CONCLUSION
Traditionally the bioactive phytochemicals plants have been continuously exploited in the field of the healthcare system for antiviral therapy. Plant product-based therapy is a preferred mode of medication that is associated with less toxicity and minimal side effects. Several phytochemicals from the mangrove source have been screened and identified for the treatment of pathogenic viruses such as influenza, dengue, chikungunya, HIV, SARS-CoV-2 and so on. Mangrove plants have been used as a traditional medicine for a long day, however, specifically the anti-viral compounds from the mangrove plant are less exploited. In this chapter, a compressive review has been made to provide some of the important information about the mangrove plants and their phytochemical constituents used as anti-viral agents. Additionally, the common extraction and screening procedures that are frequently used for phytochemicals have been presented. Also, the challenges and opportunities associated with the discovery of bioactive compounds from mangrove plants have been discussed. Moreover, this chapter provides a thorough analysis and discussion of different types of mangrove plants and their specific phytochemicals that contain the metabolite having anti-viral properties by narrating the recent literature. It is expected that the scientific analysis and screening of novel mangrove phytochemicals can be suitably used for the development of potential antiviral drugs.
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Phytochemicals From Mangroves and Their Anti-Viral Applications
ACKNOWLEDGMENT
This research was supported by the OURIIP- SEED FUND grant, sponsored by Odisha State Higher Education Council, Government of Odisha, India (OURIIP Seed fund -2020/06-Biotechnology).
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Chapter 19
Anticancer Effect of
tagala
and
Curcuma caesia
Acting Through Tumor
Necrosis Factor-α:
Mediated Nuclear Factor κB Pathway
Khetbadei Lysinia Hynniewta Hadem
North Eastern Hill University, India
Lakhon Kma
North Eastern Hill University, India
Rajeshwar N. Sharan
North Eastern Hill University, India
Arnab Sen
Indian Council of Agricultural Research, Research Center for North East Region, India
Aristolochia
ABSTRACT
This chapter begins with a brief description of the events associated with carcinogenesis such as what led a normal cell to transform into a pre-neoplastic one, their multiplication, and development into cancer. The authors also described how reactive oxygen species (ROS) are generated endogenously and from carcinogens, their role in carcinogenesis, and the link between inflammation and cancer. Elucidation of how cancer arises contributes to understanding the molecular mechanisms of action of some natural products. Herbal natural products contain metabolites that exert a physiological action on human body. These metabolites are used therapeutically in modern medical practices to prevent and cure various diseases including cancer. This chapter discusses the anticancer property of two herbal plants Aristolochia tagala Cham. and Curcuma caesia Roxb. in diethylnitrosamine-induced mouse liver cancer and describes the most probable molecular mechanisms of action of the metabolites present in these plants contributing to their anticancer effect.
DOI: 10.4018/978-1-6684-5129-8.ch019
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Anticancer Eect of Aristolochia tagala and Curcuma caesia Acting Through Tumor Necrosis Factor-α
INTRODUCTION
Carcinogenesis is a term that describes the process that occurs during tumor cell transformation. Both genetic and epigenetic factors are involved in the disruption of normal cell growth and its control leading to the development of cancer. These factors play a role in each of the different stages of carcinogenesis which are initiation, promotion and progression. A change in the genetic makeup of cell can lead to alterations of four broad categories of cancer genes, namely the activation of oncogenes, inactivation of tumor suppressors, evasion of apoptosis genes, and defective DNA repair genes (Malarkey et al., 2013). Selective clonal expansion of mutated cells leads to the appearance of a benign lesion or preneoplastic focus and rapid growth of these cells enhances the probability of accumulation of additional genetic damage (Mehta, 1995; Gomes-Carneiro et al., 1997). Additional mutations and structural variation in chromosomes lead to a formation of neoplastic and metastasized cells which are invasive, fast growing and have biochemical, metabolically and morphological characteristics different from normal healthy cells (Pitot & Dragan, 1991; Butterworthet al., 1998, Klaunig et al., 2000).
Endogenous and environmental factors are known to play a role in the progression of carcinogenesis which involves different biochemical mechanism and genetic elements. Endogenous factors include un­avoidable spontaneous mutations that arise as a result of random errors in DNA replication, hormonal imbalance, growth factors and complex endogenous processes like ageing, inflammation, and obesity. These factors are together influenced by the exogenous or environmental factors and hereditary (Pitot, 1991; Wu et al., 2018). Many environmental factors have been shown to be carcinogenic. The environ- mental factors can be broadly divided into (a) Physical factors which comprises of ionizing radiations (IR) and UV light (b) Chemical factors like benzo[α] pyrene, heterocyclic amine, ethyl alcohol, aflatoxin, asbestos, cadmium, etc. and (c) Biological factors likehepatitis B virus, hepatitis C virus, epstein-Barr virus (EBV), human herpesvirus 8 (HHV-8), HTLV-1 (human T-lymphotrophic virus type 1), human papilloma virus (HPV).
ROS INVOLVEMENT IN CARCINOGENESIS
Reactive oxygen species collectively refers to radicals, ions or molecules that have a single unpaired electron in their outermost shell of electrons. ROS are unstable and highly reactive. Superoxide (O
•
hydroxyl radical ( categorized as free oxygen radicals. Hydrogen peroxide (H
), organic hydroperoxides (ROOH), hypochloride (HOCl) etc. are categorized as non-radical ROS
(O
3
(Liou & Storz, 2010).
ROS are produced endogenously as byproducts of oxygen metabolism. During mitochondrial oxidative metabolism, single electron reduction of O The mitochondrial electron transport chain is the major contributor of endogenous ROS in mammalian tissues (Saybaşili et al., 2001; St-Pierre et al., 2002; Klaunig & Kamendulis, 2004). Enzymatic reac­tions catalysed by NADPH oxidase, xanthine oxidase, lipoxygenases and cylooxgenases within the cells also contributes to the ROS pool (Babior, 1999; Griendling et al., 2000; Curtin et al., 2002; Schrader & Fahimi, 2006; Sharan et al., 2011). Superoxide can be converted to hydrogen peroxide (H al.,2008) and H terbourn, 1995).
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OH), nitric oxide (NO•), organic radicals (R•), peroxyl radicals (ROO•), etc. are
), singlet oxygen (1O2), ozone/trioxygen
2O2
leads to the production of O
2
generated can be converted to hydroxyl free radicals via the Fenton reaction (Win-
2O2
•-
in the mitochondrial matrix.
2
) (Juarez et
2O2
•−
2
367
),