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  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Schema
  9. External Links
  10. Analytics And Tracking
  11. Libraries
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We are analyzing https://link.springer.com/article/10.1186/s40170-021-00276-3.

Title:
MicroRNA-377-3p inhibits hepatocellular carcinoma growth and metastasis through negative regulation of CPT1C-mediated fatty acid oxidation | Cancer & Metabolism
Description:
Background Altered lipid metabolism is closely related to the occurrence and development of hepatocellular carcinoma (HCC). Carnitine palmitoyltransferase 1C (CPT1C) is a member of CPT1 family and plays a key role in cancer development and progression. However, how microRNAs (miRNAs) regulate CPT1C-mediated fatty acid transport and oxidation remains to be elucidated. Methods Oil Red O staining, mitochondrial, and lipid droplets immunofluorescence staining were used to detect the functions of miR-377-3p and CPT1C in fatty acid oxidation. Colocalization of palmitate and mitochondria was performed to investigate the function of miR-377-3p and CPT1C in fatty acid transport into mitochondria. Fatty acid oxidation (FAO) assay was used to detect the function of miR-377-3p and CPT1C in FAO. Cell proliferation, migration and invasion assays and animal experiments were used to evaluate the role of miR-377-3p/CPT1C axis in HCC progression in vitro and in vivo. Immunofluorescence staining was used to identify the clinical significance of miR-377-3p and CPT1C in HCC patients. Results MiR-377-3p inhibits CPT1C expression by targeting its 3’-untranslated region. Through repression of CPT1C, miR-377-3p suppresses fatty acid oxidation by preventing fatty acid from entering into mitochondria and decreasing ATP production in HCC cells. Inhibiting fatty acid oxidation abolishes the ability of miR-377-3p/CPT1C axis to regulate HCC proliferation, migration, invasion and metastasis in vitro and in vivo. In HCC patients, CPT1C is significantly upregulated, and miR-377-3p expression and lipid droplets are negatively correlated with CPT1C expression. High expression of miR-377-3p and CPT1C predict better and worse clinical outcomes, respectively. Conclusions We uncover the key function and the relevant mechanisms of the miR-377-3p/CPT1C axis in HCC, which might provide a potential target for the treatment of HCC.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Science
  • Education
  • Photography

Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {πŸ“ˆ}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,642,828 visitors per month in the current month.

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How Does Link.springer.com Make Money? {πŸ’Έ}

The income method remains a mystery to us.

While many websites aim to make money, others are created to share knowledge or showcase creativity. People build websites for various reasons. This could be one of them. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

Keywords {πŸ”}

cptc, mirp, cells, expression, hcc, lipid, cell, pubmed, cancer, article, fatty, fao, acid, google, scholar, proliferation, migration, fig, tumor, invasion, oxidation, mitochondria, assay, cas, data, hepg, metabolism, metastasis, axis, growth, mirpcptc, supplementary, droplet, carnitine, control, regulates, figure, central, results, utr, mhcch, shown, mimics, analysis, hepatocellular, carcinoma, transfected, etomoxir, content, inhibitor,

Topics {βœ’οΈ}

regulating mir-377-3p/fgfr1/erk axis mir-377-3p inhibitor-mediated enhancement cpt1a-mediated fat oxidation mir-377-3p/cpt1c axis regulates mir-377-3p-mediated cell proliferation wnt/beta-catenin signaling formalin-fixed paraffin-embedded samples recombinant vectors cpt1c-wild-type lihua ding mir-377-3p inhibitor reduced quantitative real-time pcr mir-148a targets hmgcr mir-377-3p significantly inhibited mir-377-3p inhibitor promoted mir-377-3p-transfected cells reversed mir-377-3p/cpt1c axis mir-377-3p regulates fao mir-377-3p mimics inhibited mir-377-3p suppresses proliferation mir-377-3p targeted lasp1 real-time qpcr reactions brain-expressed protein related mir-377-3p-transfected cells rescued mir-377-3p targets cpt1c hek-293t cell showed kaplan-meier survival curves mir-377-3p mimics increased mir-377-3p decreased transport abolished cpt1c-mediated fao mir-377-3p inhibitor group fatty acid oxidation mir-377-3p target site fatty acid metabolism kaplan-meier survival analysis mir-377-3p repressed fao mir-377-3p regulated fao mir-377-3p-induced suppression anti-mouse horseradish peroxidase results mir-377-3p targets mito-tracker red cmxros mir-377-3p-induced reduction hcc-related risk factors primary liver cancer carnitine palmitoyltransferase 1c recent research showed differentiated 3t3-l1 adipocyte central nervous system article download pdf tumor growth curves rate-limiting fao enzyme

Schema {πŸ—ΊοΈ}

WebPage:
      mainEntity:
         headline:MicroRNA-377-3p inhibits hepatocellular carcinoma growth and metastasis through negative regulation of CPT1C-mediated fatty acid oxidation
         description:Altered lipid metabolism is closely related to the occurrence and development of hepatocellular carcinoma (HCC). Carnitine palmitoyltransferase 1C (CPT1C) is a member of CPT1 family and plays a key role in cancer development and progression. However, how microRNAs (miRNAs) regulate CPT1C-mediated fatty acid transport and oxidation remains to be elucidated. Oil Red O staining, mitochondrial, and lipid droplets immunofluorescence staining were used to detect the functions of miR-377-3p and CPT1C in fatty acid oxidation. Colocalization of palmitate and mitochondria was performed to investigate the function of miR-377-3p and CPT1C in fatty acid transport into mitochondria. Fatty acid oxidation (FAO) assay was used to detect the function of miR-377-3p and CPT1C in FAO. Cell proliferation, migration and invasion assays and animal experiments were used to evaluate the role of miR-377-3p/CPT1C axis in HCC progression in vitro and in vivo. Immunofluorescence staining was used to identify the clinical significance of miR-377-3p and CPT1C in HCC patients. MiR-377-3p inhibits CPT1C expression by targeting its 3’-untranslated region. Through repression of CPT1C, miR-377-3p suppresses fatty acid oxidation by preventing fatty acid from entering into mitochondria and decreasing ATP production in HCC cells. Inhibiting fatty acid oxidation abolishes the ability of miR-377-3p/CPT1C axis to regulate HCC proliferation, migration, invasion and metastasis in vitro and in vivo. In HCC patients, CPT1C is significantly upregulated, and miR-377-3p expression and lipid droplets are negatively correlated with CPT1C expression. High expression of miR-377-3p and CPT1C predict better and worse clinical outcomes, respectively. We uncover the key function and the relevant mechanisms of the miR-377-3p/CPT1C axis in HCC, which might provide a potential target for the treatment of HCC.
         datePublished:2022-01-20T00:00:00Z
         dateModified:2022-01-20T00:00:00Z
         pageStart:1
         pageEnd:16
         license:http://creativecommons.org/publicdomain/zero/1.0/
         sameAs:https://doi.org/10.1186/s40170-021-00276-3
         keywords:
            Hepatocellular carcinoma
            miR-377-3p
            CPT1C
            Fatty acid oxidation
            Tumor growth
            Metastasis
            Cancer Research
            Oncology
            Metabolomics
            Metabolic Diseases
            Imaging / Radiology
            Cell Biology
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            issn:
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            type:
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               name:Ting Zhang
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                     address:
                        name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
                        type:PostalAddress
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                     name:Beijing University of Technology
                     address:
                        name:Faculty of Environment and Life, Beijing University of Technology, Beijing, China
                        type:PostalAddress
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               name:Yanan Zhang
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                        name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
                        type:PostalAddress
                     type:Organization
                     name:Beijing Institute of Basic Medical Sciences
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                        name:The Brain Science Center, Beijing Institute of Basic Medical Sciences, Beijing, China
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Jie Liu
               affiliation:
                     name:Beijing Institute of Biotechnology
                     address:
                        name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Yan Ma
               affiliation:
                     name:Beijing Institute of Biotechnology
                     address:
                        name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
                        type:PostalAddress
                     type:Organization
                     name:No. 970 Hospital of Joint Logistics Support Force of PLA
                     address:
                        name:No. 970 Hospital of Joint Logistics Support Force of PLA, Yantai, China
                        type:PostalAddress
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                     address:
                        name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
                        type:PostalAddress
                     type:Organization
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               name:Xinlong Yan
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                     name:Beijing University of Technology
                     address:
                        name:Faculty of Environment and Life, Beijing University of Technology, Beijing, China
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               name:Lihua Ding
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                     name:Beijing Institute of Biotechnology
                     address:
                        name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
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ScholarlyArticle:
      headline:MicroRNA-377-3p inhibits hepatocellular carcinoma growth and metastasis through negative regulation of CPT1C-mediated fatty acid oxidation
      description:Altered lipid metabolism is closely related to the occurrence and development of hepatocellular carcinoma (HCC). Carnitine palmitoyltransferase 1C (CPT1C) is a member of CPT1 family and plays a key role in cancer development and progression. However, how microRNAs (miRNAs) regulate CPT1C-mediated fatty acid transport and oxidation remains to be elucidated. Oil Red O staining, mitochondrial, and lipid droplets immunofluorescence staining were used to detect the functions of miR-377-3p and CPT1C in fatty acid oxidation. Colocalization of palmitate and mitochondria was performed to investigate the function of miR-377-3p and CPT1C in fatty acid transport into mitochondria. Fatty acid oxidation (FAO) assay was used to detect the function of miR-377-3p and CPT1C in FAO. Cell proliferation, migration and invasion assays and animal experiments were used to evaluate the role of miR-377-3p/CPT1C axis in HCC progression in vitro and in vivo. Immunofluorescence staining was used to identify the clinical significance of miR-377-3p and CPT1C in HCC patients. MiR-377-3p inhibits CPT1C expression by targeting its 3’-untranslated region. Through repression of CPT1C, miR-377-3p suppresses fatty acid oxidation by preventing fatty acid from entering into mitochondria and decreasing ATP production in HCC cells. Inhibiting fatty acid oxidation abolishes the ability of miR-377-3p/CPT1C axis to regulate HCC proliferation, migration, invasion and metastasis in vitro and in vivo. In HCC patients, CPT1C is significantly upregulated, and miR-377-3p expression and lipid droplets are negatively correlated with CPT1C expression. High expression of miR-377-3p and CPT1C predict better and worse clinical outcomes, respectively. We uncover the key function and the relevant mechanisms of the miR-377-3p/CPT1C axis in HCC, which might provide a potential target for the treatment of HCC.
      datePublished:2022-01-20T00:00:00Z
      dateModified:2022-01-20T00:00:00Z
      pageStart:1
      pageEnd:16
      license:http://creativecommons.org/publicdomain/zero/1.0/
      sameAs:https://doi.org/10.1186/s40170-021-00276-3
      keywords:
         Hepatocellular carcinoma
         miR-377-3p
         CPT1C
         Fatty acid oxidation
         Tumor growth
         Metastasis
         Cancer Research
         Oncology
         Metabolomics
         Metabolic Diseases
         Imaging / Radiology
         Cell Biology
      image:
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         name:Cancer & Metabolism
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            Periodical
            PublicationVolume
      publisher:
         name:BioMed Central
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            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Ting Zhang
            affiliation:
                  name:Beijing Institute of Biotechnology
                  address:
                     name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
                     type:PostalAddress
                  type:Organization
                  name:Beijing University of Technology
                  address:
                     name:Faculty of Environment and Life, Beijing University of Technology, Beijing, China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Yanan Zhang
            affiliation:
                  name:Beijing Institute of Biotechnology
                  address:
                     name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
                     type:PostalAddress
                  type:Organization
                  name:Beijing Institute of Basic Medical Sciences
                  address:
                     name:The Brain Science Center, Beijing Institute of Basic Medical Sciences, Beijing, China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Jie Liu
            affiliation:
                  name:Beijing Institute of Biotechnology
                  address:
                     name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Yan Ma
            affiliation:
                  name:Beijing Institute of Biotechnology
                  address:
                     name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
                     type:PostalAddress
                  type:Organization
                  name:No. 970 Hospital of Joint Logistics Support Force of PLA
                  address:
                     name:No. 970 Hospital of Joint Logistics Support Force of PLA, Yantai, China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Qinong Ye
            affiliation:
                  name:Beijing Institute of Biotechnology
                  address:
                     name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
            name:Xinlong Yan
            affiliation:
                  name:Beijing University of Technology
                  address:
                     name:Faculty of Environment and Life, Beijing University of Technology, Beijing, China
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
            name:Lihua Ding
            url:http://orcid.org/0000-0002-5280-8162
            affiliation:
                  name:Beijing Institute of Biotechnology
                  address:
                     name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
                     type:PostalAddress
                  type:Organization
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         name:Faculty of Environment and Life, Beijing University of Technology, Beijing, China
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         name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
         type:PostalAddress
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      address:
         name:The Brain Science Center, Beijing Institute of Basic Medical Sciences, Beijing, China
         type:PostalAddress
      name:Beijing Institute of Biotechnology
      address:
         name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
         type:PostalAddress
      name:Beijing Institute of Biotechnology
      address:
         name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
         type:PostalAddress
      name:No. 970 Hospital of Joint Logistics Support Force of PLA
      address:
         name:No. 970 Hospital of Joint Logistics Support Force of PLA, Yantai, China
         type:PostalAddress
      name:Beijing Institute of Biotechnology
      address:
         name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
         type:PostalAddress
      name:Beijing University of Technology
      address:
         name:Faculty of Environment and Life, Beijing University of Technology, Beijing, China
         type:PostalAddress
      name:Beijing Institute of Biotechnology
      address:
         name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
         type:PostalAddress
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      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Ting Zhang
      affiliation:
            name:Beijing Institute of Biotechnology
            address:
               name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
               type:PostalAddress
            type:Organization
            name:Beijing University of Technology
            address:
               name:Faculty of Environment and Life, Beijing University of Technology, Beijing, China
               type:PostalAddress
            type:Organization
      name:Yanan Zhang
      affiliation:
            name:Beijing Institute of Biotechnology
            address:
               name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
               type:PostalAddress
            type:Organization
            name:Beijing Institute of Basic Medical Sciences
            address:
               name:The Brain Science Center, Beijing Institute of Basic Medical Sciences, Beijing, China
               type:PostalAddress
            type:Organization
      name:Jie Liu
      affiliation:
            name:Beijing Institute of Biotechnology
            address:
               name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
               type:PostalAddress
            type:Organization
      name:Yan Ma
      affiliation:
            name:Beijing Institute of Biotechnology
            address:
               name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
               type:PostalAddress
            type:Organization
            name:No. 970 Hospital of Joint Logistics Support Force of PLA
            address:
               name:No. 970 Hospital of Joint Logistics Support Force of PLA, Yantai, China
               type:PostalAddress
            type:Organization
      name:Qinong Ye
      affiliation:
            name:Beijing Institute of Biotechnology
            address:
               name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Xinlong Yan
      affiliation:
            name:Beijing University of Technology
            address:
               name:Faculty of Environment and Life, Beijing University of Technology, Beijing, China
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Lihua Ding
      url:http://orcid.org/0000-0002-5280-8162
      affiliation:
            name:Beijing Institute of Biotechnology
            address:
               name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
      name:Faculty of Environment and Life, Beijing University of Technology, Beijing, China
      name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
      name:The Brain Science Center, Beijing Institute of Basic Medical Sciences, Beijing, China
      name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
      name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
      name:No. 970 Hospital of Joint Logistics Support Force of PLA, Yantai, China
      name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China
      name:Faculty of Environment and Life, Beijing University of Technology, Beijing, China
      name:Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China

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