Creative Biolabs-Immuno-oncology

FGFR1/2/3/4 Mutant Cell Panel Screening Service

Introduction

Fibroblast Growth Factor Receptors (FGFRs) are vital components of cellular signaling, encompassing four main types: FGFR1, FGFR2, FGFR3, and FGFR4. These transmembrane receptor tyrosine kinases are intrinsically involved in key biological processes such as cell proliferation, differentiation, angiogenesis, and development. Their activation involves binding with fibroblast growth factors (FGFs) which leads to dimerization, trans-autophosphorylation, and subsequent initiation of downstream signaling pathways, including RAS/MAPK and PI3K/AKT pathways. Physiological and pathological variants in these pathways significantly influence cellular behavior and are pivotal in oncogenesis across various cancers, especially through mutations and gene amplifications. In the context of cancer treatment, FGFR-targeted therapies have emerged as promising interventions. FGFR inhibitors have demonstrated efficacy in clinical trials, represent significant advancements in targeting FGFR mutations.

Fig.1 FGFR signal and inhibitors. (OA Literature)Fig.1 FGFR signal pathway and targeted-inhibitors.1

FGFR1/2/3/4 Mutant Cell Panel Screening Service at Creative Biolabs

At Creative Biolabs, we offer an advanced FGFR1/2/3/4 Mutant Cell Panel Screening Service designed to advance cancer research and therapeutic development. This service is tailored to evaluate the functional impact and drug sensitivity of a wide array of FGFR mutations. Through cutting-edge high-throughput screening methodologies, our platform facilitates the comprehensive assessment of FGFR alterations.

The utility of our cell panel screening service lies in its meticulous construction, leveraging next-generation sequencing and sophisticated bioinformatics tools. This empowers researchers to elucidate the transforming potentials of FGFR variants and their responses to FGFR-targeted modalities. Such insights can drive the discovery of novel therapeutics with enhanced specificity and efficacy against FGFR-mutated cancers.

Key Features

The FGFR1/2/3/4 Mutant Cell Panel Screening at Creative Biolabs encompasses several key features:

High-throughput Functional Assays

Evaluation of mutation-driven oncogenesis and sensitivity to targeted therapies, ensuring precise and reliable data.

Customizable Screening Panels

Tailored services to meet specific research needs, including custom mutant selections and assay configurations.

Drug Sensitivity Profiling

Systematic testing of FGFR inhibitors for efficacy against specific mutations, facilitating the identification of resistant variants and responsive therapeutics.

Applications of FGFR1/2/3/4 Mutant Cell Panel Screening

The applications of FGFR Mutant Cell Panel Screening are multifaceted and crucial for advancing cancer therapeutics:

Frequently Asked Questions

Q1: Why are FGFR mutations critical in cancer research?

A1: FGFR mutations drive key oncogenic processes, making them vital targets for therapeutic intervention. Their role in tumors' proliferation and survival underlies the need to explore targeted treatments.

Q2: How does the cell panel screening enhance FGFR-targeted drug efficacy?

A2: Our screening identifies specific mutations responsive or resistant to drugs, enabling the formulation of more effective and personalized treatment plans.

Q3: Can this service support early-phase drug discovery?

A3: Absolutely. By elucidating the interaction between FGFR mutations and novel inhibitors, our service facilitates the early-phase evaluation and optimization of potential drug candidates.

Creative Biolabs remains committed to advancing cancer research through innovative FGFR mutational screening solutions. Our services not only support new therapeutic developments but also contribute to scientific understanding, paving the way for breakthroughs in personalized cancer therapy.

Reference

  1. Zhang, Pei, et al. "Targeting FGFR for cancer therapy." Journal of Hematology & Oncology 17.1 (2024): 39. Distributed under Open Access License CC BY 4.0, without modification.

For Research Use Only | Not For Clinical Use

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