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Krüppel-like factor 4 (KLF4) activates the transcription of the gene for the platelet isoform of phosphofructokinase (PFKP) in breast cancer

Authors
 Jong-Seok Moon  ;  Hee Eun Kim  ;  Eunjin Koh  ;  Sahng Wook Park  ;  Kyung-Sup Kim  ;  Se Ho Park  ;  Won-Ji Jin  ;  Byeong-Woo Park 
Citation
 JOURNAL OF BIOLOGICAL CHEMISTRY, Vol.286(27) : 23808-23816, 2011 
Journal Title
JOURNAL OF BIOLOGICAL CHEMISTRY
ISSN
 0021-9258 
Issue Date
2011
MeSH
BreastNeoplasms ; Cell Line, Tumor ; Female ; GeneExpression Regulation, Enzymologic* ; GeneExpression Regulation, Neoplastic* ; Glucose/genetics ; Glucose/metabolism ; Glycolysis/genetics ; Humans ; Kruppel-LikeTranscriptionFactors/genetics ; Kruppel-LikeTranscriptionFactors/metabolism* ; Lactic Acid/metabolism ; Phosphofructokinase-1, Type C/biosynthesis* ; Phosphofructokinase-1, Type C/genetics ; Promoter Regions, Genetic* ; Transcription, Genetic*
Keywords
Breast Cancer ; Cell Metabolism ; Glycolysis ; Phosphofructokinase ; Transcription Regulation
Abstract
Krüppel-like factor 4 (KLF4) is a transcription factor that plays an important role in cell differentiation, proliferation, and survival, especially in the context of cancers. This study revealed that KLF4 activates glycolytic metabolism in breast cancer cells by up-regulating the platelet isoform of phosphofructokinase (PFKP). KLF4 activated the transcription of the PFKP gene by directly binding to the PFKP promoter. Whereas glucose uptake and lactate production were inhibited by the knockdown of KLF4, they were activated by the overexpression of KLF4. Unlike PFKP, the expressions of the other isoforms of phosphofructokinase and glycolytic genes were unaffected by KLF4. The human breast cancer tissues showed a close correlation between KLF4 and PFKP expression. This study also showed that PFKP plays a critical role in cell proliferation in breast cancer cells. In conclusion, it is suggested that KLF4 plays a role in maintenance of high glycolytic metabolism by transcriptional activation of the PFKP gene in breast cancer cells.
Files in This Item:
T201101611.pdf Download
DOI
10.1074/jbc.M111.236737
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Biochemistry and Molecular Biology (생화학-분자생물학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
Yonsei Authors
Koh, Eun Jin(고은진) ORCID logo https://orcid.org/0000-0001-8967-6266
Kim, Kyung Sup(김경섭) ORCID logo https://orcid.org/0000-0001-8483-8537
Kim, Hee Eun(김희은)
Moon, Jong-Seok(문종석)
Park, Byeong Woo(박병우) ORCID logo https://orcid.org/0000-0003-1353-2607
Park, Sahng Wook(박상욱) ORCID logo https://orcid.org/0000-0002-9594-7074
Park, Se Ho(박세호) ORCID logo https://orcid.org/0000-0001-8089-2755
Jin, Won Ji(진원지)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/93364
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