Investigating regulated signaling pathways in therapeutic targeting of non-small cell lung carcinoma

Copyright © 2023 The Authors. Published by Elsevier Masson SAS.. All rights reserved..

Non-small cell lung carcinoma (NSCLC) is the most common malignancy worldwide. The signaling cascades are stimulated via genetic modifications in upstream signaling molecules, which affect apoptotic, proliferative, and differentiation pathways. Dysregulation of these signaling cascades causes cancer-initiating cell proliferation, cancer development, and drug resistance. Numerous efforts in the treatment of NSCLC have been undertaken in the past few decades, enhancing our understanding of the mechanisms of cancer development and moving forward to develop effective therapeutic approaches. Modifications of transcription factors and connected pathways are utilized to develop new treatment options for NSCLC. Developing designed inhibitors targeting specific cellular signaling pathways in tumor progression has been recommended for the therapeutic management of NSCLC. This comprehensive review provided deeper mechanistic insights into the molecular mechanism of action of various signaling molecules and their targeting in the clinical management of NSCLC.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:161

Enthalten in:

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie - 161(2023) vom: 15. Mai, Seite 114452

Sprache:

Englisch

Beteiligte Personen:

Alam, Manzar [VerfasserIn]
Hasan, Gulam Mustafa [VerfasserIn]
Eldin, Sayed M [VerfasserIn]
Adnan, Mohd [VerfasserIn]
Riaz, Muhammad Bilal [VerfasserIn]
Islam, Asimul [VerfasserIn]
Khan, Ilyas [VerfasserIn]
Hassan, Md Imtaiyaz [VerfasserIn]

Links:

Volltext

Themen:

Apoptosis
Cancer signaling
Journal Article
Non-small cell lung carcinoma
Review
Small molecule inhibitors
Targeted therapy, Drug development

Anmerkungen:

Date Completed 03.04.2023

Date Revised 03.04.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.biopha.2023.114452

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM35383873X