Re-establishing the comprehension of phytomedicine and nanomedicine in inflammation-mediated cancer signaling

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Journal Title
Journal ISSN
Volume Title
A2 Katsausartikkeli tieteellisessä aikakauslehdessä
Date
2022-11
Department
Department of Applied Physics
Major/Subject
Mcode
Degree programme
Language
en
Pages
19
1086-1104
Series
SEMINARS IN CANCER BIOLOGY, Volume 86
Abstract
Recent mounting evidence has revealed extensive genetic heterogeneity within tumors that drive phenotypic variation affecting key cancer pathways, making cancer treatment extremely challenging. Diverse cancer types display resistance to treatment and show patterns of relapse following therapy. Therefore, efforts are required to address tumor heterogeneity by developing a broad-spectrum therapeutic approach that combines targeted therapies. Inflammation has been progressively documented as a vital factor in tumor advancement and has consequences in epigenetic variations that support tumor instigation, encouraging all the tumorigenesis phases. Increased DNA damage, disrupted DNA repair mechanisms, cellular proliferation, apoptosis, angiogenesis, and its incursion are a few pro-cancerous outcomes of chronic inflammation. A clear understanding of the cellular and molecular signaling mechanisms of tumor-endorsing inflammation is necessary for further expansion of anti-cancer therapeutics targeting the crosstalk between tumor development and inflammatory processes. Multiple inflammatory signaling pathways, such as the NF-κB signaling pathway, JAK-STAT signaling pathway, MAPK signaling, PI3K/AKT/mTOR signaling, Wnt signaling cascade, and TGF-β/Smad signaling, have been found to regulate inflammation, which can be modulated using various factors such as small molecule inhibitors, phytochemicals, recombinant cytokines, and nanoparticles (NPs) in conjugation to phytochemicals to treat cancer. Researchers have identified multiple targets to specifically alter inflammation in cancer therapy to restrict malignant progression and improve the efficacy of cancer therapy. siRNA-and shRNA-loaded NPs have been observed to downregulate STAT3 signaling pathways and have been employed in studies to target tumor malignancies. This review highlights the pathways involved in the interaction between tumor advancement and inflammatory progression, along with the novel approaches of nanotechnology-based drug delivery systems currently used to target inflammatory signaling pathways to combat cancer.
Description
Funding Information: Dr. Niraj Kumar Jha is thankful to Sharda University for the infrastructure and facility. The Deanship of Scientific Research (DSR) at King Abdulaziz University, Jeddah, Saudi Arabia has funded this project under grant (FP-82-42). Kavindra Kesari and Janne Ruokolainen thanking Aalto University for providing open access support. The authors would like to acknowledge the support from their respective institutes throughout the review writing process. Publisher Copyright: © 2022 The Author(s)
Keywords
Cancer signaling, Cancer therapeutics, Inflammation, Nanomedicine, Phytomedicine
Other note
Citation
Jha, N K, Arfin, S, Jha, S K, Kar, R, Dey, A, Gundamaraju, R, Ashraf, G M, Gupta, P K, Dhanasekaran, S, Abomughaid, M M, Das, S S, Singh, S K, Dua, K, Roychoudhury, S, Kumar, D, Ruokolainen, J, Ojha, S & Kesari, K K 2022, ' Re-establishing the comprehension of phytomedicine and nanomedicine in inflammation-mediated cancer signaling ', SEMINARS IN CANCER BIOLOGY, vol. 86, pp. 1086-1104 . https://doi.org/10.1016/j.semcancer.2022.02.022