Highlights on selected growth factors and their receptors as promising anticancer drug targets
Related Experiment Video
Updated: Oct 19, 2025

Utilizing Functional Genomics Screening to Identify Potentially Novel Drug Targets in Cancer Cell Spheroid Cultures
Published on: December 26, 2016
Mohammed A Mansour1, Valentina S Caputo2, Eiman Aleem2
1Cancer Biology and Therapy Lab, Division of Human Sciences, School of Applied Sciences, London South Bank University, London, UK; Biochemistry Division, Department of Chemistry, Faculty of Science, Tanta University, Tanta 31527, Egypt.
Abstract:
Growth factor receptors (GFRs) and receptor tyrosine kinases (RTK) are groups of proteins mediating a plethora of physiological processes, including cell growth, proliferation, survival, differentiation and migration. Under certain circumstances, expression of GFRs and subsequently their downstream kinase signaling are deregulated by genetic, epigenetic, and somatic changes leading to uncontrolled cell division in many human diseases, most notably cancer. Cancer cells rely on growth factors to sustain the increasing need to cell division and metabolic reprogramming through cancer-associated activating mutations of their receptors (i.e., GFRs). In this review, we highlight the recent advances of selected GFRs and their ligands (growth factors) in cancer with emphasis on structural and functional differences. We also interrogate how overexpression and/or hyperactivation of GFRs contribute to cancer initiation, development, progression, and resistance to conventional chemo- and radiotherapies. Novel approaches are being developed as anticancer agents to target growth factor receptors and their signaling pathways in different cancers. Here, we illustrate how the current knowledge of GFRs biology, and their ligands lead to development of targeted therapies to inhibit and/or block the activity of growth factors, GFRs and downstream kinases to treat diseases such as cancer.
Insights
Growth factor receptors (GFRs) and receptor tyrosine kinases (RTKs) are key proteins in cell regulation. Deregulation of GFRs drives cancer, leading to new targeted therapies blocking growth factor signaling.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Growth factor receptors (GFRs) and receptor tyrosine kinases (RTKs) regulate vital cellular functions like growth, proliferation, and survival.
- Dysregulation of GFRs and their signaling pathways, often through genetic mutations, is a hallmark of many human cancers, driving uncontrolled cell division.
- Cancer cells exploit GFRs and their ligands to sustain rapid proliferation and metabolic reprogramming.
Purpose of the Study:
- To review recent advances in understanding selected GFRs and their ligands in cancer.
- To explore the structural and functional differences of GFRs and their roles in cancer development.
- To discuss how GFR overexpression/hyperactivation contributes to cancer initiation, progression, and therapeutic resistance.
Main Methods:
- Literature review focusing on recent advances in GFRs and their ligands in cancer.
- Analysis of structural and functional differences of key GFRs.
- Interrogation of the role of GFRs in cancer initiation, progression, and resistance to therapy.
Main Results:
- GFRs and their ligands play a critical role in cancer cell proliferation, survival, and migration.
- Overexpression and hyperactivation of GFRs contribute significantly to cancer development and progression.
- GFR signaling pathways are implicated in resistance to conventional cancer treatments.
Conclusions:
- Targeted therapies aimed at inhibiting GFRs and their downstream signaling pathways represent a promising strategy for cancer treatment.
- Understanding GFR biology and ligand interactions is crucial for developing effective targeted anticancer agents.
- Novel therapeutic approaches are emerging to block growth factor, GFR, and kinase activity in various cancers.
More Related Videos
13:18Network Pharmacology Prediction and Experimental Validation of Trichosanthes-Fritillaria thunbergii Action Mechanism Against Lung Adenocarcinoma
Published on: March 3, 2023
10:46A Flow Cytometry-Based Cell Surface Protein Binding Assay for Assessing Selectivity and Specificity of an Anticancer Aptamer
Published on: September 13, 2022
Related Concept Videos
Mitogens and the Cell Cycle
Targeted Cancer Therapies
There are several types of targeted therapies against...
Transducer Mechanism: Enzyme-Linked Receptors
Major types that are helpful drug targets include:
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Abnormal Proliferation
Cancer-Critical Genes II: Tumor Suppressor Genes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...