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

Rama Rao Malla1, Vasudevaraju Padmaraju2, Rakshmitha Marni1

  • 1Cancer Biology Lab, Department of Biochemistry and Bioinformatics, GIS, GITAM (Deemed to be University), Visakhapatnam, Andhra Pradesh 530045, India; Department of Biochemistry and Bioinformatics, GIS, GITAM (Deemed to be) University, Visakhapatnam, Andhra Pradesh 530045, India.

Abstract

Insights

Long non-coding RNAs (lncRNAs) in the tumor microenvironment (TME) are key targets for natural compounds. These compounds can manage lung cancer stem cells (CSCs), offering new therapeutic strategies for drug-resistant lung cancer.

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • Lung cancer remains a major global health challenge with high mortality.
  • Long non-coding RNAs (lncRNAs) are increasingly recognized as critical regulators of cancer stem cells (CSCs) within the tumor microenvironment (TME).
  • Natural products show potential in modulating TME functions and impacting cancer progression.

Purpose of the Study:

  • To identify tumor microenvironment (TME)-related long non-coding RNAs (lncRNAs) as novel therapeutic targets.
  • To explore the potential of natural compounds in managing lung cancer through targeting lncRNAs and cancer stem cells (CSCs).

Main Methods:

  • A comprehensive literature review was conducted using keywords related to TME, lung CSCs, lncRNAs, natural products, and targeted delivery.
  • Databases searched included Scopus, Web of Science, PubMed, and Google Scholar.
  • The review focused on the role of CSCs in reprogramming the lung TME and the impact of natural products on these processes.

Main Results:

  • Tumor microenvironment (TME)-associated oncogenic and tumor suppressor lncRNAs and their pathways are crucial for maintaining stemness in lung cancer.
  • Natural phenolic compounds like curcumin, genistein, quercetin, epigallocatechin gallate, and ginsenoside Rh2 effectively manage lung CSCs.
  • These compounds modulate lncRNAs and upstream mediators via signaling and epigenetic pathways, with nanotechnology offering enhanced delivery.

Conclusions:

  • Tumor microenvironment (TME)-related lncRNAs represent promising therapeutic targets for lung cancer.
  • Natural product-based therapies hold potential for treating metastatic and drug-resistant lung cancers by targeting these lncRNAs.
  • Further development of natural product therapeutics is warranted for effective lung cancer management.

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