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P-glycoprotein: new insights into structure, physiological function, regulation and alterations in disease
Iman Imtiyaz Ahmed Juvale1, Azzmer Azzar Abdul Hamid2, Khairul Bariyyah Abd Halim3
1Department of Neurosciences, School of Medical Sciences, Universiti Sains Malaysia Health Campus, Kubang Kerian, Kota Bharu, 16150, Kelantan, Malaysia.
Multidrug resistance, a major pharmaceutical threat, is often caused by P-glycoprotein transporters. Recent research is revealing the structure and function of this crucial protein involved in health and disease.
Area of Science:
- Biochemistry
- Molecular Biology
- Pharmacology
Background:
- Multidrug resistance (MDR) poses a significant challenge to the pharmaceutical industry and disease treatment.
- MDR is frequently mediated by multidrug transporters, such as P-glycoprotein, which actively efflux compounds from cells.
- P-glycoprotein's broad substrate specificity and involvement in various physiological processes highlight its importance.
Purpose of the Study:
- To review the discovery and structural elucidation of P-glycoprotein.
- To explore the regulatory mechanisms governing P-glycoprotein expression.
- To discuss the multifaceted role of P-glycoprotein in both health and disease states.
Main Methods:
- Literature review of P-glycoprotein research.
- Analysis of structural and functional studies.
- Examination of regulatory pathways and disease implications.
Main Results:
- P-glycoprotein is a key transporter implicated in multidrug resistance.
- Recent advancements have shed light on P-glycoprotein's structure and mechanisms.
- P-glycoprotein plays vital physiological roles and its dysregulation contributes to disease.
Conclusions:
- Understanding P-glycoprotein is critical for combating multidrug resistance.
- P-glycoprotein's diverse functions necessitate further investigation.
- Targeting P-glycoprotein offers potential therapeutic strategies for various diseases.
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