Uk study shows cell signaling interaction may prevent key step in lung cancer progression
University of Kentucky HealthCare News Nov 16, 2017
New findings from University of Kentucky faculty published in the journal Scientific Reports reveals a novel cell signaling interaction that may prevent a key step in lung cancer progression.
Kentucky continues to lead the nation in incidence and death rates from lung cancer, and the UK College of Pharmacy is committed to reducing these numbers. A collaboration between the UK College of Pharmacy and the Department of Statistics in the UK College of Arts and Sciences is working to address this problem. The project is the work of Madeline Krentz Gober, a recent graduate of the UK College of PharmacyÂs Graduate Program in the lab of pharmacy faculty member Penni Black. Staff scientist James Collard and UK College of Arts and Sciences faculty member Katherine Thompson also contributed to the findings.
Previous work from the group established that a collection of microRNAsÂsmall RNA that plays a role in regulating biological process like growth and proliferationÂcould predict sensitivity of non-small cell lung cancer cells to erlotinib, a drug that is effective in treating lung cancer in certain patients.
Further investigation into this collection of microRNA genes revealed a previously unknown relationship between the role of transforming growth factor TGFbeta in initiating metastasis and epidermal growth factor receptor (EGFR) signaling non-small cell lung cancers.
Essentially, microRNA molecules that alter TGFbeta activity may prevent a key step in metastasis for cancer progression known as epithelial-mesenchymal transition, and this interaction may also require the activity of EGFR, perhaps unappreciated in the initiation of metastasis.
ÂGetting the right drugs in the right patients is critical to improving cancer outcomes," said Jill Kolesar, co-director of the Molecular Tumor Board at the UK Markey Cancer Center. "Dr. BlackÂs work is an important step in predicting which patients benefit most from erlotinib treatment.Â
Ongoing work in the Black lab seeks to uncover biomarkers of response and toxicity to new immunotherapeutic agents used in the fight against lung cancer.
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Kentucky continues to lead the nation in incidence and death rates from lung cancer, and the UK College of Pharmacy is committed to reducing these numbers. A collaboration between the UK College of Pharmacy and the Department of Statistics in the UK College of Arts and Sciences is working to address this problem. The project is the work of Madeline Krentz Gober, a recent graduate of the UK College of PharmacyÂs Graduate Program in the lab of pharmacy faculty member Penni Black. Staff scientist James Collard and UK College of Arts and Sciences faculty member Katherine Thompson also contributed to the findings.
Previous work from the group established that a collection of microRNAsÂsmall RNA that plays a role in regulating biological process like growth and proliferationÂcould predict sensitivity of non-small cell lung cancer cells to erlotinib, a drug that is effective in treating lung cancer in certain patients.
Further investigation into this collection of microRNA genes revealed a previously unknown relationship between the role of transforming growth factor TGFbeta in initiating metastasis and epidermal growth factor receptor (EGFR) signaling non-small cell lung cancers.
Essentially, microRNA molecules that alter TGFbeta activity may prevent a key step in metastasis for cancer progression known as epithelial-mesenchymal transition, and this interaction may also require the activity of EGFR, perhaps unappreciated in the initiation of metastasis.
ÂGetting the right drugs in the right patients is critical to improving cancer outcomes," said Jill Kolesar, co-director of the Molecular Tumor Board at the UK Markey Cancer Center. "Dr. BlackÂs work is an important step in predicting which patients benefit most from erlotinib treatment.Â
Ongoing work in the Black lab seeks to uncover biomarkers of response and toxicity to new immunotherapeutic agents used in the fight against lung cancer.
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