To Investigate Growth Factor Receptor Targets and Generate Cancer Targeting Inhibitors

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Receptor tyrosine kinase (RTK) regulates multiple pathways, including Mitogenactivated protein kinases (MAPKs), PI3/AKT, JAK/STAT pathway, etc. which has a significant role in the progression and metastasis of tumor. As RTK activation regulates numerous essential bodily processes, including cell proliferation and division, RTK dysregulation has been identified in many types of cancers. Targeting RTK is a significant challenge in cancer due to the abnormal upregulation and downregulation of RTK receptors subfamily EGFR, FGFR, PDGFR, VEGFR, and HGFR in the progression of cancer, which is governed by multiple RTK receptor signalling pathways and impacts treatment response and disease progression. In this review, an extensive focus has been carried out on the normal and abnormal signalling pathways of EGFR, FGFR, PDGFR, VEGFR, and HGFR and their association with cancer initiation and progression. These are explored as potential therapeutic cancer targets and therefore, the inhibitors were evaluated alone and merged with additional therapies in clinical trials aimed at combating global cancer.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:23

Enthalten in:

Current topics in medicinal chemistry - 23(2023), 30 vom: 02., Seite 2877-2972

Sprache:

Englisch

Beteiligte Personen:

Basu, Debroop [VerfasserIn]
Pal, Riya [VerfasserIn]
Sarkar, Maitrayee [VerfasserIn]
Barma, Soubhik [VerfasserIn]
Halder, Sumit [VerfasserIn]
Roy, Harekrishna [VerfasserIn]
Nandi, Sisir [VerfasserIn]
Samadder, Asmita [VerfasserIn]

Links:

Volltext

Themen:

Cancer treatment.
EC 2.7.10.1
EC 2.7.10.2
EGFR
ErbB Receptors
FGFR
HGFR
Janus Kinases
Journal Article
PDGFR
Potential inhibitors
Protein Kinase Inhibitors
RTK
Receptor Protein-Tyrosine Kinases
Review
STAT Transcription Factors
VEGFR

Anmerkungen:

Date Completed 16.01.2024

Date Revised 16.01.2024

published: Print

Citation Status MEDLINE

doi:

10.2174/0115680266261150231110053650

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM366553542