Jianrong Lu

ORCID: 0000-0002-4969-6040
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Cancer, Hypoxia, and Metabolism
  • Epigenetics and DNA Methylation
  • Cancer Cells and Metastasis
  • Histone Deacetylase Inhibitors Research
  • RNA modifications and cancer
  • Cancer-related gene regulation
  • Genomics and Chromatin Dynamics
  • Lung Cancer Treatments and Mutations
  • Metabolism, Diabetes, and Cancer
  • Muscle Physiology and Disorders
  • Hippo pathway signaling and YAP/TAZ
  • ATP Synthase and ATPases Research
  • Microtubule and mitosis dynamics
  • Genetic factors in colorectal cancer
  • Congenital heart defects research
  • Cancer-related molecular mechanisms research
  • Advanced biosensing and bioanalysis techniques
  • Tissue Engineering and Regenerative Medicine
  • MicroRNA in disease regulation
  • Neonatal Respiratory Health Research
  • Ubiquitin and proteasome pathways
  • DNA and Nucleic Acid Chemistry
  • Signaling Pathways in Disease
  • Mitochondrial Function and Pathology
  • Angiogenesis and VEGF in Cancer

University of Florida
2015-2024

Florida College
2010-2024

University of Florida Health
2013-2024

Nanjing Drum Tower Hospital
2016-2024

Chinese Academy of Medical Sciences & Peking Union Medical College
2024

Harbin Medical University
2024

Shaanxi Provincial People's Hospital
2022-2023

Nanyang Normal University
2022

UF Health Cancer Center
2018-2021

Institute of Genetics
2021

Myocyte enhancer factor-2 (MEF2) transcription factors control muscle-specific and growth factor-inducible genes. We show that hypertrophic of cardiomyocytes in response to phenylephrine serum is accompanied by activation MEF2 through a posttranslational mechanism mediated calcium, calmodulin-dependent protein kinase (CaMK), mitogen-activated (MAPK) signaling. CaMK stimulates activity dissociating class II histone deacetylases (HDACs) from the DNA-binding domain. MAPKs, which activate...

10.1073/pnas.080064097 article EN Proceedings of the National Academy of Sciences 2000-03-28

Paclitaxel (Taxol) is an effective chemotherapeutic agent for treatment of cancer patients. Despite impressive initial clinical responses, the majority patients eventually develop some degree resistance to Taxol-based therapy. The mechanisms underlying cells Taxol are not fully understood. MicroRNA (miRNA) has emerged play important roles in tumorigenesis and drug resistance. However, interaction between development miRNA been previously explored. In this study we utilized a array compare...

10.1074/jbc.m109.083337 article EN cc-by Journal of Biological Chemistry 2010-05-12

Abstract Background Taxol is one of the most effective chemotherapeutic agents for treatment patients with breast cancer. Despite impressive clinical responses initially, majority eventually develop resistance to Taxol. Lactate dehydrogenase-A (LDH-A) predominant isoforms LDH expressed in tissue, which controls conversion pyruvate lactate and plays an important role glucose metabolism. In this study we investigated LDH-A mediating human cancer cells. Results Taxol-resistant subclones,...

10.1186/1476-4598-9-33 article EN cc-by Molecular Cancer 2010-02-09

The LKB1 tumor suppressor gene is frequently mutated and inactivated in non-small cell lung cancer (NSCLC). Loss of promotes progression influences therapeutic responses preclinical studies; however, specific targeted therapies for with inactivation are currently unavailable. Here, we have identified a long noncoding RNA (lncRNA) signature that associated the loss function. We discovered LINC00473 consistently most highly induced LKB1-inactivated human primary NSCLC samples derived lines....

10.1172/jci85250 article EN Journal of Clinical Investigation 2016-05-02

ABSTRACT The embryonic vasculature develops from endothelial cells that form a primitive vascular plexus which recruits smooth muscle to the arterial and venous systems. MADS-box transcription factor MEF2C is expressed in developing (SMCs), as well surrounding mesenchyme, during embryogenesis. Targeted deletion of mouse gene resulted severe abnormalities lethality homozygous mutants by day 9.5. Endothelial were present able differentiate, but failed organize normally into plexus, did not...

10.1242/dev.125.22.4565 article EN Development 1998-11-15

PICK1 is a protein kinase C (PKC) α-binding initially identified using the yeast two-hybrid system. Here we report that contains PDZ domain interacts specifically with previously unidentified PDZ-binding (QSAV) at extreme COOH terminus of PKCα and mutation putative carboxylate-binding loop within abolishes this interaction. The in absent from other PKC isoforms do not interact PICK1. We also demonstrate can homooligomerize through sequences are distinct loop, suggesting self-association...

10.1074/jbc.272.51.32019 article EN cc-by Journal of Biological Chemistry 1997-12-01

Members of the GATA family zinc finger transcription factors have been shown to play important roles in control gene expression a variety cell types. GATA-1, -2, and -3 are expressed primarily hematopoietic lineages required for proliferation differentiation multiple types, whereas GATA-4, -5, -6 heart, where they activate cardiac muscle structural genes. Friend GATA-1 (FOG) is multitype protein that interacts with serves as cofactor GATA-1-mediated transcription. FOG coexpressed developing...

10.1128/mcb.19.6.4495 article EN Molecular and Cellular Biology 1999-06-01

The class II histone deacetylases (HDACs) 4, 5, and 7 share a common structural organization, with carboxyl-terminal catalytic domain an amino-terminal extension that mediates interactions members of the myocyte enhancer factor-2 (MEF2) family transcription factors. Association these HDACs MEF2 factors represses target genes. MEF2-interacting repressor (MITR) shares homology extensions also acts as transcriptional repressor, but lacks deacetylase domain. This suggests MITR by recruiting...

10.1074/jbc.m007364200 article EN cc-by Journal of Biological Chemistry 2001-01-01

Histone deacetylase 6 (HDAC6) is a cytoplasmic that uniquely catalyzes alpha-tubulin deacetylation and promotes cell motility. However, the mechanism underlying HDAC6-dependent migration role for microtubule acetylation in motility are not known. Here we show HDAC6-induced global was sufficient to stimulate migration. Unexpectedly, response growth factor stimulation, HDAC6 underwent rapid translocation actin-enriched membrane ruffles subsequently became associated with macropinosomes,...

10.1128/mcb.00393-07 article EN Molecular and Cellular Biology 2007-10-16

Cancer cells exhibit altered glucose metabolism characterized by a preference for aerobic glycolysis or the Warburg effect, and resist matrix detachment-induced apoptosis, which is called anoikis, barrier to metastasis. It remains largely unclear whether tumor influences anoikis Here we show that when detached from matrix, untransformed mammary epithelial undergo metabolic reprogramming markedly upregulating pyruvate dehydrogenase (PDH) kinase 4 (PDK4) through estrogen-related receptor gamma...

10.1128/mcb.06248-11 article EN Molecular and Cellular Biology 2012-03-20

Members of the MyoD family basic helix-loop-helix (bHLH) transcription factors control formation all skeletal muscles in vertebrates, but little is known molecules or mechanisms that confer unique identities to different types muscles. MyoR and capsulin are related bHLH expressed specific facial muscle precursors. We show missing mice lacking both , reflecting absence gene expression ablation corresponding myogenic lineages. These findings identify as for development head

10.1126/science.1078273 article EN Science 2002-12-20

Normal cells require adhesion to extracellular matrix for survival. Cell detachment causes a drastic increase in reactive oxygen species (ROS) that promotes anoikis. In the present study, we observed upon from matrix, human mammary epithelial strongly upregulate manganese superoxide dismutase (MnSOD, or SOD2), principal mitochondrial antioxidant enzyme detoxifies ROS through dismutation of superoxide. Induction MnSOD by cell is dependent on NFκB transcription factor. Detachment potently...

10.1038/cddis.2013.20 article EN cc-by Cell Death and Disease 2013-02-21
Coming Soon ...