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Published on: September 25, 2018
Meloxicam inhibits the growth of non-small cell lung cancer
Y Tsubouchi1, S Mukai, Y Kawahito
1First Department of Internal Medicine, Kyoto Prefectural University of Medicine, Japan.
Abstract:
Cyclooxygenase (COX)-2 has been reported to play an important role in carcinogenesis. Meloxicam (preferential COX-2 inhibitor) inhibits the growth of COX-2 positive and COX-1 negative colorectal cancer cells. We evaluated the effects of meloxicam on the growth of lung cancer cells. By reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blot analysis, COX-2 but not COX-1 was expressed in human non-small cell lung cancer (NSCLC) cell lines (A549 and PC14). In human small cell lung cancer (SCLC) cell line (H841), both COX-1 and COX-2 were not detected. MTT assay and prostaglandin (PG) E2 enzyme immunoassay showed that meloxicam inhibited the growth and PGE2 production of both A549 and PC14, but not H841 cells. These findings suggest that COX-2 may play an important role in the pathogenesis and progression of NSCLC, and that meloxicam may be a useful therapeutic agents in the treatment of NSCLC.
Insights
Meloxicam, a cyclooxygenase-2 (COX-2) inhibitor, effectively reduced the growth of non-small cell lung cancer (NSCLC) cells. This suggests COX-2 plays a role in NSCLC, and meloxicam may be a potential therapeutic agent.
Area of Science:
- Oncology
- Pharmacology
Background:
- Cyclooxygenase (COX)-2 is implicated in carcinogenesis.
- Meloxicam is a preferential COX-2 inhibitor with known effects on colorectal cancer cells.
Purpose of the Study:
- To investigate the effects of meloxicam on lung cancer cell growth.
- To determine the expression of COX-1 and COX-2 in lung cancer cell lines.
Main Methods:
- Reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blot analysis were used to assess COX expression.
- MTT assays and prostaglandin E2 enzyme immunoassays evaluated cell growth and PGE2 production.
Main Results:
- COX-2 was expressed in non-small cell lung cancer (NSCLC) cell lines (A549, PC14), but not in small cell lung cancer (SCLC) cells (H841).
- Meloxicam inhibited the growth and prostaglandin E2 production in A549 and PC14 cells, but not in H841 cells.
Conclusions:
- COX-2 appears to be involved in the pathogenesis and progression of NSCLC.
- Meloxicam demonstrates potential as a therapeutic agent for NSCLC treatment.
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