Beneficial Effects of PIN1 Inhibition on Diabetes Mellitus: A Concise Review

Meeramol C Chellappan1, Soumya Vasu1, Shriraam Mahadevan2

  • 1Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Sri Ramachandra Institute of Higher Education and Research, (DU) Porur-600 116, Chennai, India.

Insights

Type 2 diabetes mellitus (T2DM) management is challenging due to combinatorial therapy side effects. This review explores the protein interacting with NIMA (PIN1) enzyme as a potential therapeutic target for T2DM and related disorders.

Area of Science:

  • Biochemistry
  • Endocrinology
  • Molecular Biology

Background:

  • Type 2 diabetes mellitus (T2DM) is a chronic condition requiring complex management, often involving combinatorial therapies with significant side effects like weight gain and hypoglycemia.
  • Current T2DM treatments face limitations due to short-lived effectiveness and adverse effects, necessitating novel therapeutic strategies.
  • The protein interacting with NIMA (PIN1) enzyme has emerged as a potential factor in T2DM pathogenesis and associated complications.

Purpose of the Study:

  • To review the existing literature on the role of PIN1 in the progression of T2DM.
  • To examine the correlation between PIN1 activity and diabetes-related disorders.
  • To explore the potential of PIN1 as a therapeutic target for T2DM management.

Main Methods:

  • Literature review of studies investigating PIN1's role in T2DM.
  • Analysis of research on PIN1 substrates and their involvement in metabolic pathways.
  • Examination of evidence linking PIN1 to diabetes-related complications.

Main Results:

  • PIN1 interacts with various substrates implicated in T2DM development and progression.
  • Evidence suggests PIN1 may influence insulin resistance and pancreatic beta-cell function.
  • PIN1 inhibition could offer a novel approach to managing T2DM and its comorbidities.

Conclusions:

  • PIN1 is a promising molecular target for T2DM therapy.
  • Targeting PIN1 may mitigate common side effects associated with current T2DM treatments.
  • Further research into PIN1 inhibition is warranted for developing effective T2DM regimens.

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