Molecular Targeting and Novel Therapeutic Approaches against Fungal Infections.


Journal

Current molecular medicine
ISSN: 1875-5666
Titre abrégé: Curr Mol Med
Pays: Netherlands
ID NLM: 101093076

Informations de publication

Date de publication:
2023
Historique:
received: 08 06 2022
revised: 08 12 2022
accepted: 09 01 2023
medline: 23 8 2023
pubmed: 22 8 2023
entrez: 22 8 2023
Statut: ppublish

Résumé

Fungal infections have become a worldwide problem due to their involvement in numerous diseases. The risk factors for fungal infections are multiple surgeries, transplant therapies, frequent administration of antibiotics, cancer treatments, and prosthetic devices. The problem of resistance in fungi against drug therapies is widespread, becoming a severe health-related problem. The study's objective was to identify molecular targets that may open new paths for fungal treatment. Several research and review articles were studied to gather information regarding the novel mechanism of antifungal drugs. However, identifying novel targets is challenging due to the similarities between host and fungal cells. Although, the plasma membrane and cell wall of fungus offer various drug targets that may target to fight against microbial infections. Unfortunately, biofilm formation and over-expression of protein are a few mechanisms through which fungi develop resistance. Despite these problems, several approaches have been working to prevent and treat fungal infections. Modifying the chemical structure of antifungal drugs may also improve their activity and pharmacokinetics. In this review article, we have discussed the molecular targets and novel techniques to be used for the development of antifungal drugs. In addition, different strategies to overcome resistance in fungi have also been described. This article may be helpful for the researchers working on the discovery and development of new antifungal works for resistance to fungal diseases.

Sections du résumé

BACKGROUND
Fungal infections have become a worldwide problem due to their involvement in numerous diseases. The risk factors for fungal infections are multiple surgeries, transplant therapies, frequent administration of antibiotics, cancer treatments, and prosthetic devices. The problem of resistance in fungi against drug therapies is widespread, becoming a severe health-related problem.
OBJECTIVE
The study's objective was to identify molecular targets that may open new paths for fungal treatment.
METHODS
Several research and review articles were studied to gather information regarding the novel mechanism of antifungal drugs. However, identifying novel targets is challenging due to the similarities between host and fungal cells. Although, the plasma membrane and cell wall of fungus offer various drug targets that may target to fight against microbial infections. Unfortunately, biofilm formation and over-expression of protein are a few mechanisms through which fungi develop resistance.
RESULTS
Despite these problems, several approaches have been working to prevent and treat fungal infections. Modifying the chemical structure of antifungal drugs may also improve their activity and pharmacokinetics. In this review article, we have discussed the molecular targets and novel techniques to be used for the development of antifungal drugs. In addition, different strategies to overcome resistance in fungi have also been described.
CONCLUSION
This article may be helpful for the researchers working on the discovery and development of new antifungal works for resistance to fungal diseases.

Identifiants

pubmed: 37606033
pii: CMM-EPUB-129964
doi: 10.2174/1566524023666230302123310
doi:

Substances chimiques

Antifungal Agents 0
Anti-Bacterial Agents 0

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

726-736

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Abhishek Kumar (A)

Department of Pharmacology, KIET School of Pharmacy, KIET Group of Institutions, Delhi-NCR, Ghaziabad- 201206, U.P., India.

Priya Bansal (P)

Department of Pharmacology, KIET School of Pharmacy, KIET Group of Institutions, Delhi-NCR, Ghaziabad- 201206, U.P., India.

Deepti Katiyar (D)

Department of Pharmacognosy, KIET School of Pharmacy, KIET Group of Institutions, Delhi-NCR, Ghaziabad-201206, U.P., India.

Surya Prakash (S)

Department of Pharmaceutical Chemistry, KIET School of Pharmacy, KIET Group of Institutions, Delhi-NCR, Ghaziabad-201206, U.P., India.

Nidagurthi Guggilla Raghavendra Rao (NG)

Department of Pharmaceutics, KIET School of Pharmacy, KIET Group of Institutions, Delhi-NCR, Ghaziabad-201206, U.P., India.

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Classifications MeSH