Mechanisms and therapeutic potential of YTHDF readers: Linking epitranscriptomics to cancer

Na Deng1,2, Qiang Sun3,4, Shuying Wang5

  • 1Key Laboratory of Molecular Pathology and Epidemiology of Gastric Cancer in Liaoning Education Department, The First Hospital of China Medical University, Shenyang, 110001, China.

Insights

YT521-B homology domain-containing family proteins (YTHDFs) are key players in RNA epigenetic modifications like m6A, influencing cancer development and treatment resistance. Targeting YTHDFs offers a promising strategy for effective cancer therapy.

Area of Science:

  • Molecular Biology
  • Cancer Biology
  • Epigenetics

Background:

  • YT521-B homology domain-containing family proteins (YTHDFs) act as effector proteins for RNA epigenetic modifications.
  • YTHDFs are involved in N6-methyladenosine (m6A), N1-methyladenosine (m1A), and 5-methylcytosine (m5C) modifications.
  • These modifications play critical roles in cancer biology and the maintenance of cancer hallmarks.

Purpose of the Study:

  • To review the regulatory mechanisms and pathological consequences of YTHDFs in tumorigenesis.
  • To explore the role of YTHDFs in therapeutic resistance.
  • To highlight the potential of targeting YTHDFs for cancer therapy.

Main Methods:

  • Literature review of accumulating evidence on YTHDFs.
  • Analysis of YTHDFs' involvement in RNA stability, translation, and metabolism.
  • Examination of YTHDFs' independent RNA epigenetic modification pathways.

Main Results:

  • YTHDFs manipulate RNA stability, translation, and metabolism.
  • YTHDFs influence tumor initiation, progression, and anti-tumor treatment efficacy.
  • YTHDFs are implicated in therapeutic resistance.

Conclusions:

  • YTHDFs are crucial in cancer development and progression.
  • Targeting YTHDFs presents a promising strategy for cancer treatment.
  • YTHDFs offer potential for eliminating tumor cells and improving treatment efficacy.

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