Emerging roles for modulation of microRNA signatures in cancer chemoprevention

K Neelakandan1, P Babu, S Nair

  • 1Cancer Discovery Biology Laboratory, Division of Molecular Medicine, Amrita Centre for Nanosciences and Molecular Medicine; Amrita Institute of Medical Sciences and Research Centre, Amrita School of Pharmacy, Amrita Vishwa Vidyapeetham University, Kerala, India.

Insights

MicroRNAs (miRNAs) are key regulators in cancer, acting as tumor promoters or suppressors. Targeting miRNAs offers a promising strategy for novel anti-cancer drug development and chemoprevention.

Area of Science:

  • Molecular Biology
  • Genetics
  • Oncology

Background:

  • MicroRNAs (miRNAs) are small non-coding RNAs regulating cellular processes vital to cancer, including proliferation, apoptosis, and angiogenesis.
  • Aberrant miRNA expression correlates with tumor development and progression, suggesting their potential as therapeutic targets.
  • Phytochemicals can modulate miRNA expression, impacting tumor growth and chemosensitivity.

Purpose of the Study:

  • To review the multifaceted roles of miRNAs in tumorigenesis and early drug discovery.
  • To explore miRNA-based anti-cancer therapies and the impact of chemopreventive agents on miRNA expression.
  • To discuss miRNA involvement in drug metabolism, cancer stem cells, epithelial-to-mesenchymal transition, glycosylation, carcinogenesis, and chemoresistance.

Main Methods:

  • Literature review of studies on miRNA function in cancer.
  • Analysis of miRNA modulation by chemopreventive phytochemicals.
  • Examination of miRNA roles in various cancer hallmarks and drug resistance.

Main Results:

  • miRNAs are implicated in diverse cancer aspects, from initiation to metastasis and drug resistance.
  • Chemopreventive agents modulate specific miRNAs, influencing cancer cell behavior.
  • miRNA dysregulation is linked to cancer stem cells, EMT, altered glycosylation, and carcinogenesis.

Conclusions:

  • miRNAs represent a promising target class for anti-cancer drug development and chemoprevention.
  • Understanding miRNA roles can lead to improved biomarker discovery and targeted therapies.
  • Modulating miRNA expression holds potential for overcoming cancer chemoresistance.

Related Concept Videos

MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA ends...
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA ends...
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
Loss of Tumor Suppressor Gene Functions01:12

Loss of Tumor Suppressor Gene Functions

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...