Therapeutic potential of FLANC, a novel primate-specific long non-coding RNA in colorectal cancer

. 2020 Oct ; 69 (10) : 1818-1831. [epub] 20200127

Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem, Research Support, U.S. Gov't, Non-P.H.S.

Perzistentní odkaz   https://www.medvik.cz/link/pmid31988194

Grantová podpora
U01 CA213759 NCI NIH HHS - United States
U54 CA210181 NCI NIH HHS - United States
U54 CA096297 NCI NIH HHS - United States
UH3 TR000943 NCATS NIH HHS - United States
R01 CA184792 NCI NIH HHS - United States
U01 CA187956 NCI NIH HHS - United States
U54 CA096300 NCI NIH HHS - United States
U01 CA196403 NCI NIH HHS - United States
R01 CA181572 NCI NIH HHS - United States
R01 CA072851 NCI NIH HHS - United States
R01 CA182905 NCI NIH HHS - United States
P30 CA016672 NCI NIH HHS - United States
R01 CA222007 NCI NIH HHS - United States
R01 CA226537 NCI NIH HHS - United States
R01 GM122775 NIGMS NIH HHS - United States

OBJECTIVE: To investigate the function of a novel primate-specific long non-coding RNA (lncRNA), named FLANC, based on its genomic location (co-localised with a pyknon motif), and to characterise its potential as a biomarker and therapeutic target. DESIGN: FLANC expression was analysed in 349 tumours from four cohorts and correlated to clinical data. In a series of multiple in vitro and in vivo models and molecular analyses, we characterised the fundamental biological roles of this lncRNA. We further explored the therapeutic potential of targeting FLANC in a mouse model of colorectal cancer (CRC) metastases. RESULTS: FLANC, a primate-specific lncRNA feebly expressed in normal colon cells, was significantly upregulated in cancer cells compared with normal colon samples in two independent cohorts. High levels of FLANC were associated with poor survival in two additional independent CRC patient cohorts. Both in vitro and in vivo experiments demonstrated that the modulation of FLANC expression influenced cellular growth, apoptosis, migration, angiogenesis and metastases formation ability of CRC cells. In vivo pharmacological targeting of FLANC by administration of 1,2-dioleoyl-sn-glycero-3-phosphatidylcholine nanoparticles loaded with a specific small interfering RNA, induced significant decrease in metastases, without evident tissue toxicity or pro-inflammatory effects. Mechanistically, FLANC upregulated and prolonged the half-life of phosphorylated STAT3, inducing the overexpression of VEGFA, a key regulator of angiogenesis. CONCLUSIONS: Based on our findings, we discovered, FLANC as a novel primate-specific lncRNA that is highly upregulated in CRC cells and regulates metastases formation. Targeting primate-specific transcripts such as FLANC may represent a novel and low toxic therapeutic strategy for the treatment of patients.

Center for Gastrointestinal Research and Center for Translational Genomics and Oncology Baylor Scott and White Health Research Institute and Charles A Sammons Cancer Center Baylor University Medical Center Dallas Texas USA

Center for RNA interference and Non coding RNA The University of Texas MD Anderson Cancer Center Houston Texas USA

Central European Institute of Technology Masaryk University Brno Czech Republic

China America Cancer Research Institute Dongguan Scientific Research Center Guangdong Medical University Dongguan China

Computational Medicine Center and Department of Pathology Anatomy and Cell Biology Thomas Jefferson University Philadelphia Pennsylvania USA

Department of Cancer Biology University of Texas MD Anderson Cancer Center Houston Texas USA

Department of Clinical Cancer Prevention University of Texas MD Anderson Cancer Center Houston Texas USA

Department of Comprehensive Cancer Care Masaryk Memorial Cancer Institute Brno Czech Republic

Department of Experimental Therapeutics University of Texas MD Anderson Cancer Center Houston Texas USA

Department of Internal Medicine Institute of Gastroenterology Yonsei University College of Medicine Seoul South Korea

Department of Medical Biology Faculty of Health Sciences UiT The Arctic University of Norway Tromsø Norway

Department of Medical Sciences University of Ferrara Ferrara Emilia Romagna Italy

Department of Molecular Diagnostics Therapeutics and Translational Oncology City of Hope National Medical Center Duarte California USA

Department of Morphology Surgery and Experimental Medicine University of Ferrara Ferrara Emilia Romagna Italy

Department of Stem Cell Transplantation University of Texas MD Anderson Cancer Center Houston Texas USA

Department of Surgery Dubrava Clinical Hospital Zagreb Croatia

Department of Surgical Oncology University of Texas MD Anderson Cancer Center Houston Texas USA

Division of Molecular Medicine Ruder Boskovic Institute Zagreb Croatia

Division of Oncology Medical University of Graz Graz Styria Austria

Gastroenterology Department Kyungpook National University Hospital; School of Medicine Kyungpook National University Daegu South Korea

Mathematics in Medicine Program The Houston Methodist Research Institute Houston Texas USA

Medical and Molecular Genetics Department Indiana University Indianapolis Indiana USA

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