Natural products: Potential targets of TME related long non-coding RNAs in lung cancer

肿瘤微环境 癌症干细胞 肺癌 癌症研究 生物 转移 癌症 医学 生物信息学 肿瘤科 内科学 肿瘤细胞
作者
Rama Rao Malla,Vasudevaraju Padmaraju,Rakshmitha Marni,Mohammad Amjad Kamal
出处
期刊:Phytomedicine [Elsevier BV]
卷期号:93: 153782-153782 被引量:8
标识
DOI:10.1016/j.phymed.2021.153782
摘要

Lung cancer is a significant health concern worldwide due to high mortality and morbidity, despite the advances in diagnosis, treatment, and management. Recent experimental evidence from different models suggested long non-coding RNAs (lncRNAs) as major modulators of cancer stem cells (CSCs) in the tumor microenvironment (TME) to support metastasis and drug resistance in lung cancer. Evidence-based studies demonstrated that natural products interfere with TME functions.To establish lncRNAs of TME as novel targets of natural compounds for lung cancer management.Current study used a combination of TME and lung CSCs, lncRNAs and enrichment and stemness maintenance, natural products and stem cell management, natural products and lncRNAs, natural products and targeted delivery as keywords to retrieve the literature from Scopus, Web of Science, PubMed, and Google Scholar. This study critically reviewed the current literature and presented cancer stem cells' ability in reprogramming lung TME.This review found that TME related oncogenic and tumor suppressor lncRNAs and their signaling pathways control the maintenance of stemness in lung TME. This review explored natural phenolic compounds and found that curcumin, genistein, quercetin epigallocatechin gallate and ginsenoside Rh2 are efficient in managing lung CSCs. They modulate lncRNAs and their upstream mediators by targeting signaling and epigenetic pathways. This review also identified relevant nanotechnology-based phytochemical delivery approaches for targeting lung cancer.By critical literature analysis, TME related lncRNAs were identified as potential therapeutic targets, aiming to develop natural product-based therapeutics to treat metastatic and drug-resistant lung cancers.
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