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New data on the regulation of the genetic activity that protects against lung cancer

A research project led by the University of Granada, which includes researchers from Harvard and Yale, has provided new data for a better understanding of the alterations produced during the development of lung cancer, the tumour with the highest yearly death rate in Spain
This research clears the path for the development of new antitumoral therapeutic strategies based on microRNAs activity
Scientists at the University of Granada, in collaboration with the universities of Harvard and Yale (United States) have provided new data for a better understanding of the alterations produced during the development of lung cancer, the tumour with the highest yearly death rate in Spain.
This research has found that certain small RNA molecules called microRNAs can deactivate the function of the SMARCA4 gene, which protects healthy cells from becoming tumour cells.
These findings, which were developed in pre-clinical models, constitute the foundation for the development of future applications for the diagnosis and prognostication of lung cancer.
“We had previously discovered that lung tumours in patients lost the activity of the SMARCA4 gene, which carries out tasks that protect normal cells from turning into tumour cells. This new research proves that this loss in the tumour-suppression activity of SMARCA4 could be attributed to the activity of certain microRNAs”, says prof. Pedro P. Medina, the principal investigator in this project, and a researcher at the Molecular Biochemistry and Biology I Department at the University of Granada.
“This result has opened up a new research line in our lab, by means of which we aim to explore new therapeutic pathways based on the regulation conducted by microRNAs”, he added.
The “Regulation of Genetic Expression and Cancer” research group is made up of young scientists recently established at the University of Granada, and it includes researchers from the Molecular Biochemistry and Biology I Department
This research has been led by prof. Pedro P. Medina, and its first authors are the University of Granada researchers Isabel Fernández and Eva Rufino, who are also members of the Molecular Biochemistry and Biology I Department. The team included researchers from the University of Valencia (Spain), the Bellvitge Institute of Biomedical Research at the University of Barcelona, as well as researchers from Yale and Harvard.
The article has been published recently in the prestigious journal Human Molecular Genetics, published by Oxford University Press, and which ranks at the top of international journals on genetics.
Bibliography:
Expression inactivation of SMARCA4 by microRNAs in lung tumors
Isabel F. Coira, Eva E. Rufino-Palomares, Octavio A. Romero, Paola Peinado, Chanatip Metheetrairut, Laura Boyero-Corral, Julian Carretero, Esther Farez-Vidal, Marta Cuadros, Fernando Reyes-Zurita, Jose A.Lupiáñez, Montse Sánchez-Cespedes, Frank J. Slack, Pedro Medina
Hum. Mol. Genet. (2014) doi: 10.1093/hmg/ddu55
The article can be downloaded here:
SWI/SNF proteins as targets in cancer therapy.
Schiaffino-Ortega S, Balinas C, Cuadros M, Medina PP.
J Hematol Oncol. 2014 Nov 13;7(1):81.
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Contact:
Pedro Medina Vico
Molecular Biochemistry and Biology I Department, University of Granada
Phone: 958 243252

A research project led by the University of Granada, which includes researchers from Harvard and Yale, has provided new data for a better understanding of the alterations produced during the development of lung cancer, the tumour with the highest yearly death rate in Spain

This research clears the path for the development of new antitumoral therapeutic strategies based on microRNAs activity 

Scientists at the University of Granada, incollaboration with the universities of Harvard and Yale (United States) have provided new data for a better understanding of the alterations produced during the development of lung cancer, the tumour with the highest yearly death rate in Spain.

This research has found that certain small RNA molecules called microRNAs can deactivate the function of the SMARCA4 gene, which protects healthy cells from becoming tumour cells.

These findings, which were developed in pre-clinical models, constitute the foundation for the development of future applications for the diagnosis and prognostication of lung cancer.

“We had previously discovered that lung tumours in patients lost the activity of the SMARCA4 gene, which carries out tasks that protect normal cells from turning into tumour cells. This new research proves that this loss in the tumour-suppression activity of SMARCA4 could be attributed to the activity of certain microRNAs”, says prof. Pedro P. Medina, the principal investigator in this project, and a researcher at the Molecular Biochemistry and Biology I Department at the University of Granada.

“This result has opened up a new research line in our lab, by means of which we aim to explore new therapeutic pathways based on the regulation conducted by microRNAs”, he added.

The “Regulation of Genetic Expression and Cancer” research group is made up of young scientists recently established at the University of Granada, and it includes researchers from the Molecular Biochemistry and Biology I Department

This research has been led by prof. Pedro P. Medina, and its first authors are the University of Granada researchers Isabel Fernández and Eva Rufino, who are also members of the Molecular Biochemistry and Biology I Department. The team included researchers from the University of Valencia (Spain), the Bellvitge Institute of Biomedical Research at the University of Barcelona, as well as researchers from Yale and Harvard. 

The article has been published recently in the prestigious journal Human Molecular Genetics, published by Oxford University Press, and which ranks at the top of international journals on genetics.

Bibliography:
Expression inactivation of SMARCA4 by microRNAs in lung tumors
Isabel F. Coira, Eva E. Rufino-Palomares, Octavio A. Romero, Paola Peinado, Chanatip Metheetrairut, Laura Boyero-Corral, Julian Carretero, Esther Farez-Vidal, Marta Cuadros, Fernando Reyes-Zurita, Jose A.Lupiáñez, Montse Sánchez-Cespedes, Frank J. Slack, Pedro Medina 
Hum. Mol. Genet. (2014) doi: 10.1093/hmg/ddu55

The article can be downloaded here:
http://hmg.oxfordjournals.org/content/early/2014/10/29/hmg.ddu554.long

SWI/SNF proteins as targets in cancer therapy.
Schiaffino-Ortega S, Balinas C, Cuadros M, Medina PP.
J Hematol Oncol. 2014 Nov 13;7(1):81. 

Research Team at the University of Granada

 

Contact: 
Pedro Medina Vico
Molecular Biochemistry and Biology I Department, University of Granada
Phone: 958 243252
Email: pedromedina@ugr.es