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Hedgehog Pathway Activation Might Mediate Pemetrexed Resistance in NSCLC Cells.
- Source :
-
Anticancer research [Anticancer Res] 2020 Mar; Vol. 40 (3), pp. 1451-1458. - Publication Year :
- 2020
-
Abstract
- Background/aim: Resistance to chemotherapeutic agents is the main cause of reduced survival in non-small cell lung cancer (NSCLC) patients. The Hedgehog (HH) pathway has been shown to be crucial in cell development and survival. Activated in several types of cancer it might be a potent bypass mechanism mediating chemotherapy resistance.<br />Materials and Methods: HCC827 NSCLC cells were treated with sub-lethal doses of pemetrexed to produce pemetrexed resistance. RT-qPCR was performed to measure gene expression of HH pathway proteins. A cell growth assay was used to measure the impact of the HH-inhibitor Gant61 in naïve and chemoresistant cell lines.<br />Results: Pemetrexed resistant cells showed significantly increased expression of HH signaling genes (GLI1, GLI2, GLI3, PTCH1, SHH). Supporting these results, pemetrexed resistant cells treated with the HH inhibitor Gant61 showed reduced proliferation compared to naïve cells.<br />Conclusion: HH pathway may play an important role in mediating pemetrexed resistance in NSCLC cells. Blocking the HH pathway may be a potential option to overcome this resistance.<br /> (Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.)
- Subjects :
- Antineoplastic Agents pharmacology
Carcinoma, Non-Small-Cell Lung drug therapy
Carcinoma, Non-Small-Cell Lung genetics
Carcinoma, Non-Small-Cell Lung metabolism
Cell Growth Processes drug effects
Cell Line, Tumor
Drug Resistance, Neoplasm
Gene Expression drug effects
Hedgehog Proteins antagonists & inhibitors
Humans
Lung Neoplasms drug therapy
Lung Neoplasms genetics
Lung Neoplasms metabolism
Pyridines pharmacology
Pyrimidines pharmacology
Signal Transduction
Hedgehog Proteins metabolism
Pemetrexed pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1791-7530
- Volume :
- 40
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Anticancer research
- Publication Type :
- Academic Journal
- Accession number :
- 32132042
- Full Text :
- https://doi.org/10.21873/anticanres.14087