MicroRNAs, Hypoxia and the Stem-Like State as Contributors to Cancer Aggressiveness

Lucy Wanjiku Macharia1,2, Caroline Muriithi Wanjiru1,3, Marianne Wanjiru Mureithi4

  • 1Instituto Estadual do Cérebro Paulo Niemeyer - Secretaria de Estado de Saúde, Rio de Janeiro, Brazil.

Frontiers in Genetics
|March 8, 2019
PubMed

Insights

MicroRNAs (miRNAs) regulate cancer. Hypoxia and cancer stem-like cells interact with miRNAs, driving aggressive tumor growth in cancers like glioblastoma.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • MicroRNAs (miRNAs) are small non-coding RNAs with critical regulatory functions in cancer, acting as oncogenes or tumor suppressors.
  • Altered miRNA expression is observed under hypoxia, a condition linked to the development of aggressive cancer stem-like cells.
  • Cancer stem-like cells possess self-renewal and tumor-sustaining capabilities, crucial for cancer development.

Purpose of the Study:

  • To elucidate the interconnected roles of miRNAs, hypoxia, and the stem-like state in promoting cancer aggressiveness.
  • To differentiate the combined impact from independent contributions of these factors.
  • To focus on aggressive tumor types including glioblastoma, cervical, prostate, and breast cancers.

Main Methods:

  • This review synthesizes findings from existing studies.
  • It analyzes the interplay between miRNA expression, hypoxic microenvironments, and cancer stem-like cell characteristics.
  • The review focuses on evidence from four specific aggressive cancers.

Main Results:

  • Hypoxia influences miRNA expression, contributing to the selection and maintenance of cancer stem-like cells.
  • The interaction between miRNAs, hypoxia, and stem-like properties enhances tumor aggressiveness.
  • These interconnected mechanisms are particularly relevant in aggressive cancers such as glioblastoma.

Conclusions:

  • MiRNAs, hypoxia, and cancer stem-like cells collectively drive tumor aggressiveness.
  • Understanding these interactions is vital for developing novel cancer prognostics, diagnostics, and therapeutics.
  • Targeting these interconnected pathways may offer new strategies to combat aggressive cancers.

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