Related Experiment Video
Updated: Jun 16, 2026

Establishing Dual Resistance to EGFR-TKI and MET-TKI in Lung Adenocarcinoma Cells In Vitro with a 2-step Dose-escalation Procedure
Published on: August 11, 2017
[The effect of simultaneously blocking target epidermal growth factor receptor tyrosine kinase and cyclooxygenase-2
Shi-sheng Li1, Xin Zhang, Jing Xu
1Department of Otorhinolaryngology, Affiliated Xiangya Hospital, Central South University, Changsha, 410008, China.
Objective:
This study was designed to prove simultaneously blocking both EGFR and COX-2-mediated pathways may be an efficient means of inhibiting cancer cell growth in NPC.
Method:
A combination of tarceva (EGFR-selective tyrosine kinase inhibitors) with celecoxib (Cox-2 inhibitor) was studied on its effects on cell growth, cell cycle progression, apoptosis and protein expression in CNE-2 cell lines by cell growth assay, flow cytometric analysis assay and Western blotting.
Result:
(1) The inhibition rate of cell growth was higher in the group treated with a combination of two agents than that the sum of rates of the two groups treated with only one agent (P < 0.05). (2) The combination of tarceva with celecoxib significantly induced G1 arrest (P < 0.05), but did not increase apoptosis rate (P > 0.05). (3) The group of combination showed less expressions of p-EGFR and COX-2 than any other group.
Conclusion:
Simultaneously blocking EGFR and COX-2 mediated pathways would significantly inhibit the growth of CNE-2 cell line, increase G1 arrest and reduce the expression levels of p-EGFR and COX-2.
Insights
Simultaneously blocking EGFR and COX-2 pathways with Tarceva and celecoxib significantly inhibits NPC cell growth. This combination therapy also induces G1 cell cycle arrest and reduces key protein expressions.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Epidermal Growth Factor Receptor (EGFR) and Cyclooxygenase-2 (COX-2) pathways are implicated in cancer progression.
- Targeting these pathways individually has shown potential in cancer treatment.
- NPC (Nasopharyngeal Carcinoma) remains a significant health concern, necessitating novel therapeutic strategies.
Purpose of the Study:
- To investigate the efficacy of simultaneously blocking EGFR and COX-2 pathways in inhibiting cancer cell growth.
- To evaluate the combined effects of Tarceva (EGFR inhibitor) and celecoxib (COX-2 inhibitor) on CNE-2 cell lines.
Main Methods:
- Utilized cell growth assays, flow cytometry for cell cycle analysis, and Western blotting for protein expression.
- Examined the impact of Tarceva and celecoxib, both individually and in combination, on CNE-2 cell lines.
- Assessed effects on cell growth, cell cycle progression, apoptosis, and levels of p-EGFR and COX-2.
Main Results:
- Combined treatment demonstrated a significantly higher inhibition rate of cell growth compared to single-agent treatments (P < 0.05).
- The combination therapy significantly induced G1 cell cycle arrest (P < 0.05) without increasing apoptosis (P > 0.05).
- Reduced expression of p-EGFR and COX-2 was observed in the combination group compared to other treatment groups.
Conclusions:
- Simultaneous blockade of EGFR and COX-2 pathways is an effective strategy for inhibiting CNE-2 cell line growth.
- Combination therapy with Tarceva and celecoxib enhances G1 cell cycle arrest.
- This approach leads to a significant reduction in p-EGFR and COX-2 expression levels.
Related Concept Videos
Mitogens and the Cell Cycle
Inhibition of Cdk Activity
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Interactions Between Signaling Pathways
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
GPCRs Regulate Adenylyl Cylase Activity
Two...
